Method for reducing tissue damage associated with ischemia-reperfusion or hypoxia injury

FIELD OF THE INVENTION
The present invention relates generally to a method for modulating the inflammatory response induced in a mammal following tissue injury. More particularly, this invention relates to a method for alleviating immune-cell mediated tissue destruction associated with the inflammatory response.
BACKGROUND OF THE INVENTION
The body's inflammatory response to tissue injury can cause significant tissue destruction, leading to loss of tissue function. Damage to cells resulting from the effects of inflammatory response e.g., by immune-cell mediated tissue destruction, has been implicated as the cause of reduced tissue function or loss of tissue function in diseases of the joints (e.g., rheumatoid and osteo-arthritis) and of many organs, including the kidney, pancreas, skin, lung and heart. For example, glomular nephritis, diabetes, inflammatory bowel disease, vascular diseases such as atheroclerosis and vasculitis, and skin diseases such as psoriasis and dermatitis are believed to result in large part from unwanted acute inflammatory reaction and fibrosis. A number of these diseases, including arthritis, psoriasis and inflammatory bowel disease are considered to be chronic inflammatory diseases. The damaged tissue also often is replaced by fibrotic tissue, e.g., scar tissue, which further reduces tissue function. Graft and transplanted organ rejection also is believed to be primarily due to the action of the body's immune/inflammatory response system.
The immune-cell mediated tissue destruction often follows an initial tissue injury or insult. The secondary damage, resulting from the inflammatory response, often is the source of significant tissue damage. Among the factors thought to mediate these damaging effects are those associated with modulating the body's inflammatory response following tissue injury, e.g., cytokines such as interleukin-1 (IL-1) and tumor necrosis factor (TNF), and oxygen-derived free radicals such as superoxide anions. These humoral agents are produced by adhering neutrophilic leukocytes or by endothelial cells and have been identified at ischemic sites upon reperfusion. Moreover, TNF concentrations are increased in humans after myocardial infarction.
A variety of lung diseases are characterized by airway inflammation, including chronic bronchitis, emphysema, idiopathic pulmonary fibrosis and asthma. Another type of lung-related inflammation disorders are inflammatory diseases characterized by a generalized, wide-spread, acute inflammatory response such as adult respiratory distress syndrome. Another dysfunction associated with the inflammatory response is that mounted in response to injury caused by hyperoxia, e.g., prolonged exposure to lethally high concentrations of O.sub.2 (95-100% O.sub.2). Similarly, reduced blood flow to a tissue (and, therefore reduced or lack of oxygen to tissues), as described below, also can induce a primary tissue injury that stimulates the inflammatory response.
It is well known that damage occurs to cells in mammals which have been deprived of oxygen. In fact, the interruption of blood flow, whether partial (hypoxia) or complete (ischemia) and the ensuing inflammatory responses may be the most important cause of coagulative necrosis or cell death in human disease. The complications of atherosclerosis, for example, are generally the result of ischemic cell injury in the brain, heart, small intestines, kidneys, and lower extremities. Highly differentiated cells, such as the proximal tubular cells of the kidney, cardiac myocytes, and the neurons of the central nervous system, all depend on aerobic respiration to produce ATP, the energy necessary to carry out their specialized functions. When ischemia limits the oxygen supply and ATP is depleted, the affected cells may become irreversibly injured. The ensuing inflammatory responses to this initial injury provide additional insult to the affected tissue. Examples of such hypoxia or ischemia are the partial or total loss of blood supply to the body as a whole, an organ within the body, or a region within an organ, such as occurs in cardiac arrest, pulmonary embolus, renal artery occlusion, coronary occlusion or occlusive stroke.
The tissue damage associated with ischemia-reperfusion injury is believed to comprise both the initial cell damage induced by the deprivation of oxygen to the cell and its subsequent recirculation, as well as the damage caused by the body's response to this initial damage. It is thought that reperfusion injury may result in dysfunction to the endothelium of the vasculature as well as injury to the surrounding tissue. In idiopathic pulmonary fibrosis, for example, scar tissue accumulates on the lung tissue lining, inhibiting the tissue's elasticity. The tissue damage associated with hyperoxia injury is believed to follow a similar mechanism, where the initial damage is mediated primarily through the presence of toxic oxygen metabolites, followed by an inflammatory response to this initial injury.
Similarly, tissues and organs for transplantation also are subject to the tissue destructive effects associated with the recipient host body's inflammatory response following transplantation. It is currently believed that the initial destructive response is due in large part to reperfusion injury to the transplanted organ after it has been transplanted to the organ recipient.
Accordingly, the success of organ or tissue transplantation depends greatly on the preservation of the tissue activity (e.g., tissue or organ viability) at the harvest of the organ, during storage of the harvested organ, and at transplantation. To date, preservation of organs such as lungs, pancreas, heart and liver remains a significant stumbling block to the successful transplantation of these organs. U.S. Pat. No. 4,952,409 describes a superoxide dismutase-containing liposome to inhibit reperfusion injury. U.S. Pat. No. 5,002,965 describes the use of ginkolides, known platelet activating factor antagonists, to inhibit reperfusion injury. Both of these factors are described as working primarily by inhibiting the release of and/or inhibiting the damaging effects of free oxygen radicals. A number of patents also have issued on the use of immunosuppressants for inhibiting graft rejection. A representative listing includes U.S. Pat. Nos. 5,104,858, 5,008,246 and 5,068,323. A significant problem with many immunosuppressants is their low therapeutic index, requiring the administration of high doses that can have significant toxic side effects.
Rheumatoid and osteoarthritis are prevalent diseases characterized by chronic inflammation of the synovial membrane lining the afflicted joint. A major consequence of chronic inflammatory joint disease (e.g., rheumatoid arthritis) and degenerative arthritis (e.g., osteoarthritis) is loss of function of those affected joints. This loss of function is due primarily to destruction of the major structural components of the joint, cartilage and bone, and subsequent loss of the proper joint anatomy. As a consequence of chronic disease, joint destruction ensues and can lead to irreversible and permanent damage to the joint and loss of function. Current treatment methods for severe cases of rheumatoid arthritis typically include the removal of the synovial membrane, e.g., synovectomy. Surgical synovectomy has many limitations, including the risk of the surgical procedure itself, and the fact that a surgeon often cannot remove all of the diseased membrane. The diseased tissue remaining typically regenerates, causing the same symptoms which the surgery was meant to alleviate.
Psoriasis is a chronic, recurrent, scaling skin disease of unknown etiology characterized by chronic inflammation of the skin. Erythematous eruptions, often in papules or plaques, and usually having a white silvery scale, can affect any part of the skin, but most commonly affect the scalp, elbows, knees and lower back. The disease usually occurs in adults, but children may also be affected. Patients with psoriasis have a much greater incidence of arthritis (psoraitic arthritis), and generalized exfoliation and even death can threaten afflicted individuals.
Current therapeutic regimens include topical or intralesional application of corticosteroids, topical administration of keratolytics, and use of tar and UV light on affected areas. No single therapy is ideal, and it is rare for a patient not to be treated with several alternatives during the relapsing and remitting course of the disease. Whereas systematic treatment can induce prompt resolution of psoriatic lesions, suppression often requires ever-increasing doses, sometimes with toxic side effect, and tapering of therapy may result in rebound phenomena with extensions of lesions, possibly to exfoliation.
Inflammatory bowel disease (IBD) describes a class of clinical disorders of the gastrointestinal mucosa characterized by chronic inflammation and severe ulceration of the mucosa. The two major diseases in this classification are ulcerative colitis and regional enteritis (Crohn's Disease). Like oral mucositis, the diseases classified as IBD are associated with severe mucosal ulceration (frequently penetrating the wall of the bowel and forming strictures and fistulas), severe mucosal and submucosal inflammation and edema, and fibrosis (e.g., scar tissue formation which interferes with the acid protective function of the gastrointestinal lining.) Other forms of IBD include regional ileitis and proctitis. Clinically, patients with fulminant IBD can be severely ill with massive diarrhea, blood loss, dehydration, weight loss and fever. The prognosis of the disease is not good and frequently requires resection of the diseased tissue.
Therefore, an object of the present invention is to provide a method for protecting mammalian tissue, particularly human tissue, from the damage associated with the inflammatory response following a tissue injury. The inflammatory reaction may be in response to an initial tissue injury or insult. The original injury may be chemically, mechanically, immunologically or biologically related. Another object is to provide methods and compositions for protecting tissue from the tissue destructive effects associated with chronic inflammatory diseases, including arthritis (e.g., reheumatoid or osteoarthritis), psoriatic arthritis, psoriasis and dermatitis, inflammatory bowel disease and other autoimmune diseases.
Another object of the invention is to provide methods and compositions for enhancing the viability of mammalian tissues and organs to be transplanted, including protecting the transplanted organs from immune cell-mediated tissue destruction, such as the tissue damage associated with ischemia-reperfusion injury, such as can occur upon initiation of blood flow after transplantation of the organ in the recipient host.
Another object of the invention is to provide a method for alleviating tissue damage associated with ischemic-reperfusion injury in a mammal following a deprivation of oxygen to a tissue in the mammal. Other objects of the present invention include providing a method for alleviating tissue damage associated with ischemic-reperfusion injury in a human which has suffered from hypoxia or ischemia following cardiac arrest, pulmonary embolus, renal artery occlusion, coronary occlusion or occlusive stroke, as well as tissue damage associated with a surgical or other aggressive clinical procedure. Still another object is to provide a method for alleviating tissue damage associated with hyperoxia-induced injury in a human following exposure to lethally high oxygen concentrations.
Still another object of the invention is to provide a method for modulating inflammatory responses in general, particularly those induced in a human following tissue injury.
These and other objects and features of the invention will be apparent from the description, drawings and claims which follow.
SUMMARY OF THE INVENTION
The present invention provides a method for alleviating the tissue destructive effects associated with activation of the inflammatory response following tissue injury. The method comprises the step of providing to the affected tissue a therapeutically effective concentration of a morphogenic protein ("morphogen", as defined herein) upon tissue injury or in anticipation of tissue injury, sufficient to substantially inhibit or reduce the tissue destructive effects of the inflammatory response.
In one aspect, the invention features compositions and therapeutic treatment methods that comprise the step of administering to a mammal a therapeutically effective amount of a morphogenic protein ("morphogen"), as defined herein, upon injury to a tissue, or in anticipation of such injury, for a time and at a concentration sufficient to inhibit the tissue destructive effects associated with the body's inflammatory response, including repairing damaged tissue, and/or inhibiting additional damage thereto.
In another aspect, the invention features compositions and therapeutic treatment methods for protecting tissues and organs from the tissue destructive effects of the inflammatory response which include administering to the mammals upon injury to a tissue or in anticipation of such injury, a compound that stimulates in vivo a therapeutically effective concentration of an endogenous morphogen within the body of the mammal sufficient to protect the tissue from the tissue destructive effects associated with the inflammatory response, including repairing damaged tissue and/or inhibiting additional damage thereto. These compounds are referred to herein as morphogen-stimulating agents, and are understood to include substances which, when administered to a mammal, act on cells of tissue(s) or organ(s) that normally are responsible for, or capable of, producing a morphogen and/or secreting a morphogen, and which cause the endogenous level of the morphogen to be altered. The agent may act, for example, by stimulating expression and/or secretion of an endogenous morphogen.
As embodied herein, the term "ischemic-reperfusion injury" refers to the initial damage associated with oxygen deprivation of a cell and the subsequent damage associated with the inflammatory response when the cell is resupplied with oxygen. As embodied herein, the term "hyperoxia-induced injury" refers to the tissue damage associated with prolonged exposure to lethally high doses of oxygen, e.g., greater than 95% O.sub.2, including the tissue damage associated with the inflammatory response to the initial toxically high oxygen concentration. Accordingly, as used herein, "toxic oxygen concentrations" refers to the tissue damage associated with the injury induced by both lethally low oxygen concentrations of oxygen (including the complete lack of oxygen), and by lethally high oxygen concentrations. The expression "alleviating" means the protection from, reduction of and/or elimination of undesired tissue destruction, particularly immune cell-mediated tissue destruction. The tissue destruction may be in response to an initial tissue injury, which may be mechanical, chemical or immunological in origin. The expression "enhance the viability of" tissues or organs, as used herein, means protection from, reduction of and/or elimination of reduced or lost tissue or organ function as a result of tissue death, particularly immune cell-mediated tissue death. "Transplanted" living tissue includes both tissue transplants, (e.g., as in the case of bone marrow transplants, for example), and tissue grafts. Finally, a "free oxygen radical inhibiting agent" means a molecule capable of inhibiting the release of and/or inhibiting the tissue damaging effects of free oxygen radicals.
In one embodiment of the invention, the invention provides methods and compositions for alleviating the ischemic-reperfusion injury in mammalian tissue resulting from a deprivation of, and subsequent reperfusion of, oxygen to the tissue. In another embodiment, the invention provides a method for alleviating the tissue-destructive effects associated with hyperoxia. In still another embodiment of the invention, the invention provides methods and compositions for maintaining the viability of tissues and organs, particularly transplanted tissues and organs, including protecting these tissues and organs from ischemia-reperfusion injury. In still another embodiment, the invention provides methods for protecting tissues and organs from the tissue destructive effects of chronic inflammatory diseases, such as arthritis, psoriasis, dermatitis, including contact dermatitis, IBD and other chronic inflammatory diseases of the gastrointestinal tract, as well as the tissue destructive effects associated with other, known autoimmune diseases, such as diabetes, multiple sclerosis, amyotrophic lateral sclerosis (ALS), and other autoimmune neurodegenerative diseases.
In one aspect of the invention, the morphogen is provided to the damaged tissue following an initial injury to the tissue. The morphogen may be provided directly to the tissue, as by injection to the damaged tissue site or by topical administration, or may be provided indirectly, e.g., systemically by oral or parenteral means. Alternatively, as described above, an agent capable of stimulating endogenous morphogen expression and/or secretion may be administered to the mammal. Preferably, the agent can stimulate an endogenous morphogen in cells associated with the damaged tissue. Alternatively, morphogen expression and/or secretion may be stimulated in a distant tissue and the morphogen transported to the damaged tissue by the circulatory system.
In another aspect of the invention, the morphogen is provided to tissue at risk of damage due to immune cell-mediated tissue destruction. Examples of such tissues include tissue grafts and transplanted tissue or organs, as well as any tissue or organ about to undergo a surgical procedure or other clinical procedure likely to either inhibit blood flow to the tissue or otherwise induce an inflammatory response. Here the morphogen or morphogen-stimulating agent preferably is provided to the patient prior to induction of the injury, e.g., as a prophylactic, to provide a cyto-protective effect to the tissue at risk.
The morphogens described herein are envisioned to be useful in enhancing viability of any organ or living tissue to be transplanted The morphogens may be used to particular advantage in lung, heart, kidney, liver and pancreas transplants, as well as in transplantation and/or grafting of skin, gastrointestinal mucosa, bone marrow and other living tissues.
Where the patient suffers from a chronic inflammatory disease, such as diabetes, arthritis, psoriasis, IBD, and the like, the morphogen or morphogen-stimulating agent preferably is administered at regular intervals as a prophylactic, to prevent and/or inhibit the tissue damage normally associated with the disease during flare periods. As above, the morphogen or morphogen-stimulating agent may be provided directly to the tissue at risk, for example by injection or by topical administration, or indirectly, as by systemic e.g., oral or parenteral administration.
Among the morphogens useful in this invention are proteins originally identified as osteogenic proteins, such as the OP-1, OP-2 and CBMP2 proteins, as well as amino acid sequence-related proteins such as DPP (from Drosophila), Vgl (from Xenopus), Vgr-1 (from mouse, see U.S. Pat. No. 5,011,691 to Oppermann et al.), GDF-1 (from mouse, see Lee (1991) PNAS 88:4250-4254), all of which are presented in Table II and Seq. ID Nos. 5-14), and the recently identified 60A protein (from Drosophila, Seq. ID No. 24, see Wharton et al. (1991) PNAS 88:9214-9218.) The members of this family, which include members of the TGF-.beta. super-family of proteins, share substantial amino acid sequence homology in their C-terminal regions. The proteins are translated as a precursor, having an N-terminal signal peptide sequence, typically less than about 30 residues, followed by a "pro" domain that is cleaved to yield the mature sequence. The signal peptide is cleaved rapidly upon translation, at a cleavage site that can be predicted in a given sequence using the method of Von Heijne ((1986) Nucleic Acids Research 14:4683-4691.) Table I, below, describes the various morphogens identified to date, including their nomenclature as used herein, their Seq. ID references, and publication sources for the amino acid sequences for the full length proteins not included in the Seq. Listing. The disclosure of these publications is incorporated herein by reference.
TABLE I______________________________________"OP-1" Refers generically to the group of morphogenically active proteins expressed from part or all of a DNA sequence encoding OP-1 protein, including allelic and species variants thereof, e.g., human OP-1 ("hOP-1", Seq. ID No. 5, mature protein amino acid sequence), or mouse OP-1 ("mOP-1", Seq. ID No, 6, mature protein amino acid sequence.) The conserved seven cysteine skeleton is defined by residues 38 to 139 of Seq. ID Nos. 5 and 6. The cDNA sequences and the amino acids encoding the full length proteins are provided in Seq. Id Nos. 16 and 17 (hOP1) and Seq. ID Nos. 18 and 19 (mOP1.) The mature proteins are defined by residues 293-431 (hOP1) and 292-430 (mOP1). The "pro" regions of the proteins, cleaved to yield the mature, morphogenically active proteins are defined essentially by residues 30-292 (hOP1) and residues 30-291 (mOP1)."OP-2" refers generically to the group of active proteins expressed from part or all of a DNA sequence encoding OP-2 protein, including allelic and species variants thereof, e.g., human OP-2 ("hOP-2", Seq. ID No. 7, mature protein amino acid sequence) or mouse OP-2 ("mOP-2", Seq. ID No. 8, mature protein amino acid sequence). The conserved seven cysteine skeleton is defined by residues 38 to 139 of Seq. ID Nos. 7 and 8. The cDNA sequences and the amino acids encoding the full length proteins are provided in Seq. ID Nos. 20 and 21 (hOP2) and Seq. ID Nos. 22 and 23 (mOP2.) The mature proteins are defined essentially by residues 264-402 (hOP2) and 261-399 (mOP2). The "pro" regions of the proteins, cleaved to yield the mature, morphogenically active proteins likely are defined essentially by residues 18-263 (hOP2) and residues 18-260 (mOP2). (Another cleavage site also occurs 21 residues upstream for both OP-2 proteins.)"CBMP2" refers generically to the morphogenically active proteins expressed from a DNA sequence encoding the CBMP2 proteins, including allelic and species variants thereof, e.g., human CBMP2A ("CBMP2A(fx)", Seq ID No. 9) or human CBMP2B DNA ("CBMP2B(fx)", Seq. ID No. 10). The amino acid sequence for the full length proteins, referred to in the literature as BMP2A and BMP2B, or BMP2 and BMP4, appear in Wozney, et al. (1988) Science 242:1528- 1534. The pro domain for BMP2 (BMP2A) likely includes residues 25-248 or 25-282; the mature protein, residues 249-396 or 283-396. The pro domain for BMP4 (BMP2B) likely includes residues 25-256 or 25-292; the mature protein, residues 257-408 or 293-408."DPP(fx)" refers to protein sequences encoded by the Drosophila DPP gene and defining the conserved seven cysteine skeleton (Seq. ID No. 11). The amino acid sequence for the full length protein appears in Padgett, et al (1987) Nature 325: 81-84. The pro domain likely extends from the signal peptide cleavage site to residue 456; the mature protein likely is defined by residues 457-588."Vgl(fx)" refers to protein sequences encoded by the Xenopus Vgl gene and defining the conserved seven cysteine skeleton (Seq. ID No. 12). The amino acid sequence for the full length protein appears in Weeks (1987) Cell 51: 861-867. The prodomain likely extends from the signal peptide cleavage site to residue 246; the mature protein likely is defined by residues 247-360."Vgr-1(fx)" refers to protein sequences encoded by the murine Vgr-1 gene and defining the conserved seven cysteine skeleton (Seq. ID No. 13). The amino acid sequence for the full length protein appears in Lyons, et al, (1989) PNAS 86: 4554-4558. The prodomain likely extends from the signal peptide cleavage site to residue 299; the mature protein likely is defined by residues 300-438."GDF-1(fx)" refers to protein sequences encoded by the human GDF-1 gene and defining the conserved seven cysteine skeleton (Seq. ID No. 14). The cDNA and encoded amino sequence for the full length protein is provided in Seq. ID. No. 32. The prodomain likely extends from the signal peptide clavage site to residue 214; the mature protein likely is defined by residues 215-372."60A" refers generically to the morphogenically active proteins expressed from part or all of a DNA sequence (from the Drosophila 60A gene) encoding the 60A proteins (see Seq. ID No. 24 wherein the cDNA and encoded amino acid sequence for the full length protein is provided). "60A(fx)" refers to the protein sequences defining the conserved seven cysteine skeleton (residues 354 to 455 of Seq. ID No. 24.) The prodomain likely extends from the signal peptide cleavage site to residue 324; the mature protein likely is defined by residues 325-455."BMP3(fx)" refers to protein sequences encoded by the human BMP3 gene and defining the conserved seven cysteine skeleton (Seq. ID No. 26). The amino acid sequence for the full length protein appears in Wozney et al. (1988) Science 242: 1528-1534. The pro domain likely extends from the signal peptide cleavage site to residue 290; the mature protein likely is defined by residues 291-472."BMP5(fx)" refers to protein sequences encoded by the human BMP5 gene and defining the conserved seven cysteine skeleton (Seq. ID No. 27). The amino acid sequence for the full length protein appears in Celeste, et al. (1991) PNAS 87: 9843-9847. The pro domain likely extends from the signal peptide cleavage site to residue 316; the mature protein likely is defined by residues 317-454."BMP6(fx)" refers to protein sequences encoded by the human BMP6 gene and defining the conserved seven cysteine skeleton (Seq. ID No. 28). The amino acid sequence for the full length protein appears in Celeste, et al. (1990) PNAS 87: 9843-5847. The pro domain likely includes extends from the signal peptide cleavage site to residue 374; the mature sequence likely includes residues 375-513.______________________________________
The OP-2 proteins have an additional cysteine residue in this region (e.g., see residue 41 of Seq. ID Nos. 7 and 8), in addition to the conserved cysteine skeleton in common with the other proteins in this family. The GDF-1 protein has a four amino acid insert within the conserved skeleton (residues 44-47 of Seq. ID No. 14) but this insert likely does not interfere with the relationship of the cysteines in the folded structure. In addition, the CBMP2 proteins are missing one amino acid residue within the cysteine skeleton.
The morphogens are inactive when reduced, but are active as oxidized homodimers and when oxidized in combination with other morphogens of this invention (e.g., asheterodimers). Thus, as defined herein, a morphogen is a dimeric protein comprising a pair of polypeptide chains, wherein each polypeptide chain comprises at least the C-terminal six cysteine skeleton defined by residues 43-139 of Seq. ID No. 5, including functionally equivalent arrangements of these cysteines (e.g., amino acid insertions or deletions which alter the linear arrangement of the cysteines in the sequence but not their relationship in the folded structure), such that, when the polypeptide chains are folded, the dimeric protein species comprising the pair of polypeptide chains has the appropriate three-dimensional structure, including the appropriate intra- or inter-chain disulfide bonds such that the protein is capable of acting as a morphogen as defined herein. Specifically, the morphogens generally are capable of all of the following biological functions in a morphogenically permissive environment: stimulating proliferation of progenitor cells; stimulating the differentiation of progenitor cells; stimulating the proliferation of differentiated cells; and supporting the growth and maintenance of differentiated cells, including the "redifferentiation" of transformed cells. In addition, it is also anticipated that these morphogens are capable of inducing redifferentiation of committed cells under appropriate environmental conditions.
In one preferred aspect, the morphogens of this invention comprise one of two species of generic amino acid sequences: Generic Sequence 1 (Seq. ID No. 1) or Generic Sequence 2 (Seq. ID No. 2); where each Xaa indicates one of the 20 naturally-occurring L-isomer, .alpha.-amino acids or a derivative thereof. Generic Sequence 1 comprises the conserved six cysteine skeleton and Generic Sequence 2 comprises the conserved six cysteine skeleton plus the additional cysteine identified in OP-2 (see residue 36, Seq. ID No. 2). In another preferred aspect, these sequences further comprise the following additional sequence at their N-terminus:
Cys Xaa Xaa Xaa Xaa (Seq. ID No. 15) 1 5
Preferred amino acid sequences within the foregoing generic sequences include: Generic Sequence 3 (Seq. ID No. 3), Generic Sequence 4 (Seq. ID No. 4), Generic Sequence 5 (Seq. ID No. 30) and Generic Sequence 6 (Seq. ID No. 31), listed below. These Generic Sequences accommodate the homologies shared among the various preferred members of this morphogen family identified in Table II, as well as the amino acid sequence variation among them. Specifically, Generic Sequences 3 and 4 are composite amino acid sequences of the following proteins presented in Table II and identified in Seq. ID Nos. 5-14: human OP-1 (hOP-1, Seq. ID Nos. 5 and 16-17), mouse OP-1 (mOP-1, Seq. ID Nos. 6 and 18-19), human and mouse OP-2 (Seq. ID Nos. 7, 8, and 20-22), CBMP2A (Seq. ID No. 9), CBMP2B (Seq. ID No. 10), DPP (from Drosophila, Seq. ID No. 11), Vgl, (from Xenopus, Seq. ID No. 12), Vgr-1 (from mouse, Seq. ID No. 13), and GDF-1 (from mouse, Seq. ID No. 14.) The generic sequences include both the amino acid identity shared by the sequences in Table II, as well as alternative residues for the variable positions within the sequence. Note that these generic sequences allow for an additional cysteine at position 41 or 46 in Generic Sequences 3 or 4, respectively, providing an appropriate cysteine skeleton where inter- or intramolecular disulfide bonds can form, and contain certain critical amino acids which influence the tertiary structure of the proteins.
______________________________________Generic Sequence 3______________________________________ Leu Tyr Val Xaa Phe 1 5Xaa Xaa Xaa Gly Trp Xaa Xaa Trp Xaa 10Xaa Ala Pro Xaa Gly Xaa Xaa Ala 15 20Xaa Tyr Cys Xaa Gly Xaa Cys Xaa 25 30Xaa Pro Xaa Xaa Xaa Xaa Xaa 35Xaa Xaa Xaa Asn His Ala Xaa Xaa 40 45Xaa Xaa Leu Xaa Xaa Xaa Xaa Xaa 50Xaa Xaa Xaa Xaa Xaa Xaa Xaa Cys 55 60Cys Xaa Pro Xaa Xaa Xaa Xaa Xaa 65Xaa Xaa Xaa Leu Xaa Xaa Xaa 70 75Xaa Xaa Xaa Xaa Val Xaa Leu Xaa 80Xaa Xaa Xaa Xaa Met Xaa Val Xaa 85 90Xaa Cys Gly Cys Xaa 95______________________________________
wherein each Xaa is independently selected from a group of one or more specified amino acids defined as follows: "Res." means "residue" and Xaa at res.4=(Ser. Asp or Glu); Xaa at res.6=(Arg, Gln, Ser or Lys); Xaa at res.7=(Asp or Glu); Xaa at res.8=(Leu or Val); Xaa at res.11=(Gln, Leu, Asp, His or Asn); Xaa at res.12=(Asp, Arg or Asn); Xaa at res.14=(Ile or Val); Xaa at res.15=(Ile or Val); Xaa at res.18=(Glu, Gln, Leu, Lys, Pro or Arg); Xaa at res.20=(Tyr or Phe); Xaa at res.21=(Ala, Ser, Asp, Met, His, Leu or Gln); Xaa at res.23=(Tyr, Asn or Phe); Xaa at res.26=(Glu, His, Tyr, Asp or Gln); Xaa at res.28=(Glu, Lys, Asp or Gln); Xaa at res.30=(Ala, Ser, Pro or Gln); Xaa at res.31=(Phe, Leu or Tyr); Xaa at res.33=(Leu or Val); Xaa at res.34=(Asn, Asp, Ala or Thr); Xaa at res.35=(Ser, Asp, Glu, Leu or Ala); Xaa at res.36=(Tyr, Cys, His, Ser or Ile); Xaa at res.37=(Met, Phe, Gly or Leu); Xaa at res.38=(Asn or Ser); Xaa at res.39=(Ala, Ser or Gly); Xaa at res.40=(Thr, Leu or Ser); Xaa at res.44=(Ile or Val); Xaa at res.45=(Val or Leu); Xaa at res.46=(Gln or Arg); Xaa at res.47=(Thr, Ala or Ser); Xaa at res.49=(Val or Met); Xaa at res.50=(His or Asn); Xaa at res.51=(Phe, Leu, Asn, Ser, Ala or Val); Xaa at res.52=(Ile, Met, Asn, Ala or Val); Xaa at res.53=(Asn, Lys, Ala or Glu); Xaa at res.54=(Pro or Ser); Xaa at res.55=(Glu, Asp, Asn, or Gly); Xaa at res.56=(Thr, Ala, Val, Lys, Asp, Tyr, Ser or Ala); Xaa at res.57=(Val, Ala or Ile); Xaa at res.58=(Pro or Asp); Xaa at res.59=(Lys or Leu); Xaa at res.60=(Pro or Ala); Xaa at res.63=(Ala or Val); Xaa at res.65=(Thr or Ala); Xaa at res.66=(Gln, Lys, Arg or Glu); Xaa at res.67=(Leu, Met or Val); Xaa at res.68=(Asn, Ser or Asp); Xaa at res.69=(Ala, Pro or Ser); Xaa at res.70=(Ile, Thr or Val); Xaa at res.71=(Ser or Ala); Xaa at res.72=(Val or Met); Xaa at res.74=(Tyr or Phe); Xaa at res.75=(Phe, Tyr or Leu); Xaa at res.76=(Asp or Asn); Xaa at res.77=(Asp, Glu, Asn or Ser); Xaa at res.78=(Ser, Gln, Asn or Tyr); Xaa at res.79=(Ser, Asn, Asp or Glu); Xaa at res.80=(Asn, Thr or Lys); Xaa at res.82=(Ile or Val); Xaa at res.84=(Lys or Arg); Xaa at res.85=(Lys, Asn, Gln or His); Xaa at res.86=(Tyr or His); Xaa at res.87=(Arg, Gln or Glu); Xaa at res.88=(Asn, Glu or Asp); Xaa at res.90=(Val, Thr or Ala); Xaa at res.92=(Arg, Lys, Val, Asp or Glu); Xaa at res.93=(Ala, Gly or Glu); and Xaa at res.97=(His or Arg);
______________________________________Generic Sequence 4______________________________________Cys Xaa Xaa Xaa Xaa Leu Tyr Val Xaa Phe 1 5 10Xaa Xaa Xaa Gly Trp Xaa Xaa Trp Xaa 15Xaa Ala Pro Xaa Gly Xaa Xaa Ala 20 25Xaa Tyr Cys Xaa Gly Xaa Cys Xaa 30 35Xaa Pro Xaa Xaa Xaa Xaa Xaa 40Xaa Xaa Xaa Asn His Ala Xaa Xaa 45 50Xaa Xaa Leu Xaa Xaa Xaa Xaa Xaa 55Xaa Xaa Xaa Xaa Xaa Xaa Xaa Cys 60 65Cys Xaa Pro Xaa Xaa Xaa Xaa Xaa 70Xaa Xaa Xaa Leu Xaa Xaa Xaa 75 80Xaa Xaa Xaa Xaa Val Xaa Leu Xaa 85Xaa Xaa Xaa Xaa Met Xaa Val Xaa 90 95Xaa Cys Gly Cys Xaa 100______________________________________
wherein each Xaa is independently selected from a group of one or more specified amino acids as defined by the following: "Res." means "residue" and Xaa at res.2=(Lys or Arg); Xaa at res.3=(Lys or Arg); Xaa at res.4=(His or Arg); Xaa at res.5=(Glu, Ser, His, Gly, Arg or Pro); Xaa at res.9=(Ser, Asp or Glu); Xaa at res.11=(Arg, Gln, Ser or Lys); Xaa at res.12=(Asp or Glu); Xaa at res.13=(Leu or Val); Xaa at res.16=(Gln, Leu, Asp, His or Asn); Xaa at res.17=(Asp, Arg, or Asn); Xaa at res.19=(Ile or Val); Xaa at res.20=(Ile or Val); Xaa at res.23=(Glu, Gln, Leu, Lys, Pro or Arg); Xaa at res.25=(Tyr or Phe); Xaa at res.26=(Ala, Ser, Asp, Met, His, Leu, or Gln); Xaa at res.28=(Tyr, Asn or Phe); Xaa at res.31=(Glu, His, Tyr, Asp or Gln); Xaa at res.33=Glu, Lys, Asp or Gln); Xaa at res.35=(Ala, Ser or Pro); Xaa at res.36=(Phe, Leu or Tyr); Xaa at res.38=(Leu or Val); Xaa at res.39=(Asn, Asp, Ala or Thr); Xaa at res.40=(Ser, Asp, Glu, Leu or Ala); Xaa at res.41=(Tyr, Cys, His, Ser or Ile); Xaa at res.42=(Met, Phe, Gly or Leu); Xaa at res.44=(Ala, Ser or Gly); Xaa at res.45=(Thr, Leu or Ser); Xaa at res.49=(Ile or Val); Xaa at res.50=(Val or Leu); Xaa at res.51=(Gln or Arg); Xaa at res.52=(Thr, Ala or Ser); Xaa at res.54=(Val or Met); Xaa at res.55=(His or Asn); Xaa at res.56=(Phe, Leu, Asn, Ser, Ala or Val); Xaa at res.57=(Ile, Met, Asn, Ala or Val); Xaa at res.58=(Asn, Lys, Ala or Glu); Xaa at res.59=(Pro or Ser); Xaa at res.60=(Glu, Asp, or Gly); Xaa at res.61=(Thr, Ala, Val, Lys, Asp, Tyr, Ser or Ala); Xaa at res.62=(Val, Ala or Ile); Xaa at res.63=(Pro or Asp); Xaa at res.64=(Lys or Leu); Xaa at res.65=(Pro or Ala); Xaa at res.68=(Ala or Val); Xaa at res.70=(Thr or Ala); Xaa at res.71=(Gln, Lys, Arg or Glu); Xaa at res.72=(Leu, Met or Val); Xaa at res.73=(Asn, Ser or Asp); Xaa at res.74=(Ala, Pro or Ser); Xaa at res.75=(Ile, Thr or Val); Xaa at res.76=(Ser or Ala); Xaa at res.77=(Val or Met); Xaa at res.79=(Tyr or Phe); Xaa at res.80=(Phe, Tyr or Leu); Xaa at res.81=(Asp or Asn); Xaa at res.82=(Asp, Glu, Asn or Ser); Xaa at res.83=(Ser, Gln, Asn or Tyr); Xaa at res.84=(Ser, Asn, Asp or Glu); Xaa at res.85=(Asn, Thr or Lys); Xaa at res.87=(Ile or Val); Xaa at res.89=(Lys or Arg); Xaa at res.90=(Lys, Asn, Gln or His); Xaa at res.91=(Tyr or His); Xaa at res.92=(Arg, Gln or Glu); Xaa at res.93=(Asn, Glu or Asp); Xaa at res.95=(Val, Thr or Ala); Xaa at res.97=(Arg, Lys, Val, Asp or Glu); Xaa at res.98=(Ala, Gly or Glu); and Xaa at res.102=(His or Arg).
Similarly, Generic Sequence 5 (Seq. ID No. 30) and Generic Sequence 6 (Seq. ID No. 31) accommodate the homologies shared among all the morphogen protein family members identified in Table II. Specifically, Generic Sequences 5 and 6 are composite amino acid sequences of human OP-1 (hOP-1, Seq. ID Nos. 5 and 16-17), mouse OP-1 (mOP-1, Seq. ID Nos. 6 and 18-19), human and mouse OP-2 (Seq. ID Nos. 7, 8, and 20-22), CBMP2A (Seq. ID No. 9), CBMP2B (Seq. ID No. 10), DPP (from Drosophila, Seq. ID No. 11), Vgl, (from Xenopus, Seq. ID No. 12), Vgr-1 (from mouse, Seq. ID No. 13), and GDF-1 (from mouse, Seq. ID No. 14), human BMP3 (Seq. ID No. 26), human BMP5 (Seq. ID No. 27), human BMP6 (Seq. ID No. 28) and 60(A) (from Drosophila, Seq. ID Nos. 24-25). The generic sequences include both the amino acid identity shared by these sequences in the C-terminal domain, defined by the six and seven cysteine skeletons (Generic Sequences 5 and 6, respectively), as well as alternative residues for the variable positions within the sequence. As for Generic Sequences 3 and 4, Generic Sequences 5 and 6 allow for an additional cysteine at position 41 (Generic Sequence 5) or position 46 (Generic Sequence 6), providing an appropriate cysteine skeleton where inter- or intramolecular disulfide bonds can form, and containing certain critical amino acids which influence the tertiary structure of the proteins.
______________________________________Generic Sequence 5______________________________________ Leu Xaa Xaa Xaa Phe 1 5Xaa Xaa Xaa Gly Trp Xaa Xaa Trp Xaa 10Xaa Xaa Pro Xaa Xaa Xaa Xaa Ala 15 20Xaa Tyr Cys Xaa Gly Xaa Cys Xaa 25 30Xaa Pro Xaa Xaa Xaa Xaa Xaa 35Xaa Xaa Xaa Asn His Ala Xaa Xaa 40 45Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa 50Xaa Xaa Xaa Xaa Xaa Xaa Xaa Cys 55 60Cys Xaa Pro Xaa Xaa Xaa Xaa Xaa 65Xaa Xaa Xaa Leu Xaa Xaa Xaa 70 75Xaa Xaa Xaa Xaa Val Xaa Leu Xaa 80Xaa Xaa Xaa Xaa Met Xaa Val Xaa 85 90Xaa Cys Xaa Cys Xaa 95______________________________________
wherein each Xaa is independently selected from a group of one or more specified amino acids defined as follows: "Res." means "residue" and Xaa at res.2=(Tyr or Lys); Xaa at res.3=Val or Ile); Xaa at res.4=(Ser, Asp or Glu); Xaa at res.6=(Arg, Gln, Ser, Lys or Ala); Xaa at res.7=(Asp, Glu or Lys); Xaa at res.8 =(Leu, Val or Ile); Xaa at res.11=(Gln, Leu, Asp, His, Asn or Ser); Xaa at res.12=(Asp, Arg, Asn or Glu); Xaa at res.14=(Ile or Val); Xaa at res.15=(Ile or Val); Xaa at res.16 (Ala or Ser); Xaa at res.18=(Glu, Gln, Leu, Lys, Pro or Arg); Xaa at res.19=(Gly or Ser); Xaa at res.20=(Tyr or Phe); Xaa at res.21=(Ala, Ser, Asp, Met, His, Gln, Leu or Gly); Xaa at res.23=(Tyr, Asn or Phe); Xaa at res.26=(Glu, His, Tyr, Asp, Gln or Ser); Xaa at res.28=(Glu, Lys, Asp, Gln or Ala); Xaa at res.30=(Ala, Ser, Pro, Gln or Asn); Xaa at res.31=(Phe, Leu or Tyr); Xaa at res.33=(Leu, Val or Met); Xaa at res.34=(Asn, Asp, Ala, Thr or Pro); Xaa at res.35=(Ser, Asp, Glu, Leu, Ala or Lys); Xaa at res.36=(Tyr, Cys, His, Ser or Ile); Xaa at res.37=(Met, Phe, Gly or Leu); Xaa at res.38=(Asn, Ser or Lys); Xaa at res.39=(Ala, Ser, Gly or Pro); Xaa at res.40=(Thr, Leu or Ser); Xaa at res.44=(Ile, Val or Thr); Xaa at res.45=(Val, Leu or Ile); Xaa at res.46=(Gln or Arg); Xaa at res.47=(Thr, Ala or Ser); Xaa at res.48=(Leu or Ile); Xaa at res.49=(Val or Met); Xaa at res.50=(His, Asn or Arg); Xaa at res.51=(Phe, Leu, Asn, Ser, Ala or Val); Xaa at res.52=(Ile, Met, Asn, Ala, Val or Leu); Xaa at res.53=(Asn, Lys, Ala, Glu, Gly or Phe); Xaa at res.54=(Pro, Ser or Val); Xaa at res.55=(Glu, Asp, Asn, Gly, Val or Lys); Xaa at res.56=(Thr, Ala, Val, Lys, Asp, Tyr, Ser, Ala, Pro or His); Xaa at res.57=(Val, Ala or Ile); Xaa at res.58=(Pro or Asp); Xaa at res.59=(Lys, Leu or Glu); Xaa at res.60=(Pro or Ala); Xaa at res.63=(Ala or Val); Xaa at res.65=(Thr, Ala or Glu); Xaa at res.66=(Gln, Lys, Arg or Glu); Xaa at res.67=(Leu, Met or Val); Xaa at res.68=(Asn, Ser, Asp or Gly); Xaa at res.69=(Ala, Pro or Ser); Xaa at res.70=(Ile, Thr, Val or Leu); Xaa at res.71=(Ser, Ala or Pro); Xaa at res.72=(Val, Met or Ile); Xaa at res.74=(Tyr or Phe); Xaa at res.75=(Phe, Tyr, Leu or His); Xaa at res.76=(Asp, Asn or Leu); Xaa at res.77=(Asp, Glu, Asn or Ser); Xaa at res.78=(Ser, Gln, Asn, Tyr or Asp); Xaa at res.79=(Ser, Asn, Asp, Glu or Lys); Xaa at res.80=(Asn, Thr or Lys); Xaa at res.82=(Ile, Val or Asn); Xaa at res.84=(Lys or Arg); Xaa at res.85=(Lys, Asn, Gln, His or Val); Xaa at res.86=(Tyr or His); Xaa at res.87=(Arg, Gln, Glu or Pro); Xaa at res.88=(Asn, Glu or Asp); Xaa at res.90=(Val, Thr, Ala or Ile); Xaa at res.92=(Arg, Lys, Val, Asp or Glu); Xaa at res.93=(Ala, Gly, Glu or Ser); Xaa at res.95=(Gly or Ala) and Xaa at res.97=(His or Arg).
______________________________________Generic Sequence 6______________________________________Cys Xaa Xaa Xaa Xaa Leu Xaa Xaa Xaa Phe 1 5 10Xaa Xaa Xaa Gly Trp Xaa Xaa Trp Xaa 15Xaa Xaa Pro Xaa Xaa Xaa Xaa Ala 20 25Xaa Tyr Cys Xaa Gly Xaa Cys Xaa 30 35Xaa Pro Xaa Xaa Xaa Xaa Xaa 40Xaa Xaa Xaa Asn His Ala Xaa Xaa 45 50Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa 55Xaa Xaa Xaa Xaa Xaa Xaa Xaa Cys 60 65Cys Xaa Pro Xaa Xaa Xaa Xaa Xaa 70Xaa Xaa Xaa Leu Xaa Xaa Xaa 75 80Xaa Xaa Xaa Xaa Val Xaa Leu Xaa 85Xaa Xaa Xaa Xaa Met Xaa Val Xaa 90 95Xaa Cys Xaa Cys Xaa 100______________________________________
wherein each Xaa is independently selected from a group of one or more specified amino acids as defined by the following: "Res." means "residue" and Xaa at res.2=(Lys, Arg, Ala or Gln); Xaa at res.3=(Lys, Arg or Met); Xaa at res.4=(His, Arg or Gln); Xaa at res.5=(Glu, Ser, His, Gly, Arg, Pro, Thr, or Tyr); Xaa at res.7=(Tyr or Lys); Xaa at res.8=(Val or Ile); Xaa at res.9=(Ser, Asp or Glu); Xaa at res.11=(Arg, Gln, Ser, Lys or Ala); Xaa at res.12=(Asp, Glu, or Lys); Xaa at res.13=(Leu, Val or Ile); Xaa at res.16=(Gln, Leu, Asp, His, Asn or Ser); Xaa at res.17=(Asp, Arg, Asn or Glu); Xaa at res.19=(Ile or Val); Xaa at res.20=(Ile or Val); Xaa at res.21=(Ala or Ser); Xaa at res.23=(Glu, Gln, Leu, Lys, Pro or Arg); Xaa at res.24=(Gly or Ser); Xaa at res.25=(Tyr or Phe); Xaa at res.26=(Ala, Ser, Asp, Met, His, Gln, Leu, or Gly); Xaa at res.28=(Tyr, Asn or Phe); Xaa at res.31=(Glu, His, Tyr, Asp, Gln or Ser); Xaa at res.33=Glu, Lys, Asp, Gln or Ala); Xaa at res.35=(Ala, Ser, Pro, Gln or Asn); Xaa at res.36=(Phe, Leu or Tyr); Xaa at res.38=(Leu, Val or Met); Xaa at res.39=(Asn, Asp, Ala, Thr or Pro); Xaa at res.40=(Ser, Asp, Glu, Leu, Ala or Lys); Xaa at res.41=(Tyr, Cys, His, Ser or Ile); Xaa at res.42=(Met, Phe, Gly or Leu); Xaa at res.43=(Asn, Ser or Lys); Xaa at res.44=(Ala, Ser, Gly or Pro); Xaa at res.45=(Thr, Leu or Ser); Xaa at res.49=(Ile, Val or Thr); Xaa at res.50=(Val, Leu or Ile); Xaa at res.51=(Gln or Arg); Xaa at res.52=(Thr, Ala or Ser); Xaa at res.53=(Leu or Ile); Xaa at res.54=(Val or Met); Xaa at res.55=(His, Asn or Arg); Xaa at res.56=(Phe, Leu, Asn, Ser, Ala or Val); Xaa at res.57=(Ile, Met, Asn, Ala, Val or Leu); Xaa at res.58=(Asn, Lys, Ala, Glu, Gly or Phe); Xaa at res.59=(Pro, Ser or Val); Xaa at res.60=(Glu, Asp, Gly, Val or Lys); Xaa at res.61=(Thr, Ala, Val, Lys, Asp, Tyr, Ser, Ala, Pro or His); Xaa at res.62=(Val, Ala or Ile); Xaa at res.63=(Pro or Asp); Xaa at res.64=(Lys, Leu or Glu); Xaa at res.65=(Pro or Ala); Xaa at res.68=(Ala or Val); Xaa at res.70=(Thr, Ala or Glu); Xaa at res.71=(Gln, Lys, Arg or Glu); Xaa at res.72=(Leu, Met or Val); Xaa at res.73=(Asn, Ser, Asp or Gly); Xaa at res.74=(Ala, Pro or Ser); Xaa at res.75=(Ile, Thr, Val or Leu); Xaa at res.76=(Ser, Ala or Pro); Xaa at res.77=(Val, Met or Ile); Xaa at res.79=(Tyr or Phe); Xaa at res.80=(Phe, Tyr, Leu or His); Xaa at res.81=(Asp, Asn or Leu); Xaa at res.82=(Asp, Glu, Asn or Ser); Xaa at res.83=(Ser, Gln, Asn, Tyr or Asp); Xaa at res.84=(Ser, Asn, Asp, Glu or Lys); Xaa at res.85=(Asn, Thr or Lys); Xaa at res.87=(Ile, Val or Asn); Xaa at res.89=(Lys or Arg); Xaa at res.90=(Lys, Asn, Gln, His or Val); Xaa at res.91=(Tyr or His); Xaa at res.92=(Arg, Gln, Glu or Pro); Xaa at res.93=(Asn, Glu or Asp); Xaa at res.95=(Val, Thr, Ala or Ile); Xaa at res.97=(Arg, Lys, Val, Asp or Glu); Xaa at res.98=(Ala, Gly, Glu or Ser); Xaa at res.100=(Gly or Ala); and Xaa at res.102=(His or Arg).
Particularly useful sequences for use as morphogens in this invention include the C-terminal domains, e.g., the C-terminal 96-102 amino acid residues of Vgl, Vgr-l, DPP, OP-1, OP-2, CBMP-2A, CBMP-2B, GDF-1 (see Table II, below, and Seq. ID Nos. 5-14), as well as proteins comprising the C-terminal domains of 60A, BMP3, BMP5 and BMP6 (see Seq. ID Nos. 24-28), all of which include at least the conserved six or seven cysteine skeleton. In addition, biosynthetic constructs designed from the generic sequences, such as COP-1, 3-5, 7, 16, disclosed in U.S. Pat. No. 5,011,691, also are useful. Other sequences include the inhibins/activin proteins (see, for example, U.S. Pat. Nos. 4,968,590 and 5,011,691). Accordingly, other useful sequences are those sharing at least 70% amino acid sequence homology or "similarity", and preferably 80% homology or similarity with any of the sequences above. These are anticipated to include allelic and species variants and mutants, and biosynthetic muteins, as well as novel members of this morphogenic family of proteins. Particularly envisioned in the family of related proteins are those proteins exhibiting morphogenic activity and wherein the amino acid changes from the preferred sequences include conservative changes, e.g., those as defined by Dayoff et al., Atlas of Protein Sequence and Structure; vol. 5, Suppl. 3, pp. 345-362, (M. O. Dayoff, ed., Nat'l BioMed. Research Fdn., Washington, D.C. 1979). As used herein, potentially useful sequences are aligned with a known morphogen sequence using the method of Needleman et al. ((1970) J. Mol. Biol. 48:443-453) and identities calculated by the Align program (DNAstar, Inc.). "Homology" or "similarity" as used herein includes allowed conservative changes as defined by Dayoff et al.
The currently most preferred protein sequences useful as morphogens in this invention include those having greater than 60% identity, preferably greater than 65% identity, with the amino acid sequence defining the conserved six cysteine skeleton of hOP1 (e.g., residues 43-139 of Seq. ID No. 5). These most preferred sequences include both allelic and species variants of the OP-1 and OP-2 proteins, including the Drosophila 60A protein. Accordingly, in another preferred aspect of the invention, useful morphogens include active proteins comprising species of polypeptide chains having the generic amino acid sequence herein referred to as "OPX", which accommodates the homologies between the various identified species of OP1 and OP2 (Seq. ID No. 29).
The morphogens useful in the methods, composition and devices of this invention include proteins comprising any of the polypeptide chains described above, whether isolated from naturally-occurring sources, or produced by recombinant DNA or other synthetic techniques, and includes allelic and species variants of these proteins, naturally-occurring or biosynthetic mutants thereof, as well as various truncated and fusion constructs. Deletion or addition mutants also are envisioned to be active, including those which may alter the conserved C-terminal cysteine skeleton, provided that the alteration does not functionally disrupt the relationship of these cysteines in the folded structure. Accordingly, such active forms are considered the equivalent of the specifically described constructs disclosed herein. The proteins may include forms having varying glycosylation patterns, varying N-termini, a family of related proteins having regions of amino acid sequence homology, and active truncated or mutated forms of native or biosynthetic proteins, produced by expression of recombinant DNA in host cells.
The morphogenic proteins can be expressed from intact or truncated cDNA or from synthetic DNAs in procaryotic or eucaryotic host cells, and purified, cleaved, refolded, and dimerized to form morphogenically active compositions. Currently preferred host cells include E. coli or mammalian cells, such as CHO, COS or BSC cells. A detailed description of the morphogens useful in the methods, compositions and devices of this invention is disclosed in copending U.S. patent application Ser. Nos. 752,764, filed Aug. 30, 1991, and 667,274, filed Mar. 11, 1991, the disclosure of which are incorporated herein by reference.
Thus, in view of this disclosure, skilled genetic engineers can isolate genes from cDNA or genomic libraries of various different species which encode appropriate amino acid sequences, or construct DNAs from oligonucleotides, and then can express them in various types of host cells, including both procaryotes and eucaryotes, to produce large quantities of active proteins capable of protecting tissues and organs from immune cell-mediated tissue destruction, including substantially inhibiting such damage and/or regenerating the damaged tissue in a variety of mammals, including humans.
The foregoing and other objects, features and advantages of the present invention will be made more apparent from the following detailed description of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 shows the cardioprotective effects of morphogen (hOP1) in a rat myocardial ischemia-reperfusion model, as evidenced by the smaller loss of myocardial creatine kinase in hOP1-treated rats;
FIG. 2 shows the effects of 20 .mu.g of morphogen (hOP1 given 24 hours prior to isolation of rat heart on endothelial-dependent vasorelaxation to acetycholine following induced ischemia-reperfusion injury;
FIG. 3 shows the effect of morphogen (hOP1) on neutrophil adherence to LTB.sub.4 -stimulated mesenteric artery endothelium in neutrophil-activated rats;
FIGS. 4 (A and B) are schematic representations of morphogen inhibition of early mononuclear phagocytic multinuclearization in vivo;
FIG. 5 graphs the effect of a morphogen (e.g., OP-1) and a placebo control on mucositic lesion formation; and
FIGS. 6 (A-D) graphs the effects of a morphogen (eg., OP-1, FIGS. 6A and 6C) and TGF-P (FIGS. 6B and 6D) on collagen (6A and 6B) and hyaluronic acid (6C and 6D) production in primary fibroblast cultures.
DETAILED DESCRIPTION OF THE INVENTION
It now has been surprisingly discovered that the morphogens defined herein are effective agents in alleviating the tissue destructive effects associated with the body's inflammatory response to tissue injury. In particular, as disclosed herein, the morphogens are capable of alleviating the necrotic tissue effects associated with the ensuing inflammatory responses that occur following an initial tissue injury.
When tissue injury occurs, whether caused by bacteria, trauma, chemicals, heat, or any other phenomenon, the body's inflammatory response is stimulated. In response to signals released from the damaged cells (e.g., cytokines), extravascularization of immune effector cells is induced. Under ordinary circumstances these invading immune effector cells kill the infectious agent and/or infected or damaged cells (through the release of killing substances such as superoxides, performs, and other antimicrobial agents stored in granules), remove the dead tissues and organisms (through phagocytosis), release various biological response modifiers that promote rapid healing and covering of the wound (quite often resulting in the formation of fibrotic scar tissue), and then, after the area is successfully healed, exit from the site of the initial insult. Once the site is perceived to be normal, the local release of inflammatory cytokines ceases and the display of adhesion molecules on the vessel endothelium returns to basal levels. In some cases, however, the zeal of these interacting signals and cellular systems, which are designed to capture and contain very rapidly multiplying infectious agents, act to the detriment of the body, killing additional, otherwise healthy, surrounding tissue. This additional unnecessary tissue death further compromises organ function and sometimes results in death of the individual. In addition, the resulting scar tissue that often forms can interfere with normal tissue function as occurs, for example, in idiopathic pulmonary fibrosis, IBD and organ cirrhosis.
The vascular endothelium constitutes the first barrier between circulating immune effector cells and extravascular tissues. Extravasation of these circulating cells requires that they bind to the vascular endothelial cells, cross the basement membrane, and enter insulted tissues e.g., by phagocytosis or protease-mediated extracellular matrix degradation. Without being limited to a particular theory, it is believed that the morphogens of this invention may modulate the inflammatory response in part by modulating the attachment of immune effector cells to the luminal side of the endothelium of blood vessels at or near sites of tissue damage and/or inflammatory lesions. Because the method reduces or prevents the attachment of immune effector cells at these sites, it also prevents the subsequent release of tissue destructive agents by these same immune effector cells at sites of tissue damage and/or inflammatory lesions. Because attachment of immune effector cells to the endothelium must precede their extravascularization, the method also prevents the initial or continued entry of these cells into extravascular sites of tissue destruction or ongoing inflammatory lesions. Therefore, the invention not only relates to a method to reduce or prevent the immune cell-mediated cellular destruction at extravascular sites of recent tissue destruction, but also relates to a method to prevent or reduce the continued entry of immune effector cells into extravascular sites of ongoing inflammatory cascades. As will be appreciated by those skilled in the art, the morphogens of this invention also may be contemplated in mechanisms for disrupting the functional interaction of immune effector cells with endothelium where the adhesion molecules are induced by means other than in response to tissue injury.
One source of tissue damage follows cell exposure to toxic oxygen concentrations, such as the tissue damage following ischemic-reperfusion tissue injury (oxygen deprivation), and following hyperoxia injury (lethally high oxygen concentrations). Accordingly, the process of the present invention provides a method for alleviating the tissue damage induced by ischemic-reperfusion injury or hyperoxia-induced injury comprising the step of administering to the afflicted individual a therapeutic amount of a morphogen prior to, during, or after damage to the affected tissue. Where the toxic oxygen concentrations may be deliberately or unavoidably induced, as by a surgical or clinical procedure, the morphogen preferably is administered prior to induction.
In addition, the morphogens described herein, in contrast to fibrogenic growth factors such as TGF-.beta., stimulate tissue morphogenesis and do not stimulate fibrosis or scar tissue formation (see Example 9, below.) Accordingly, in addition to inhibiting the tissue destructive effects associated with the inflammatory response, the morphogens further enhance the viability of damaged tissue and/or organs by stimulating the regeneration of the damaged tissue and preventing fibrogenesis.
The morphogens described herein also can inhibit epithelial cell proliferation (see Example 10, below.) This activity of the morphogens also may be particularly useful in the treatment of psoriasis and other inflammatory diseases that involve epithelial cell populations.
Provided below are detailed descriptions of suitable morphogens useful in the methods and compositions of this invention, as well as methods for their administration and application, and numerous, nonlimiting examples which 1) illustrate the suitability of the morphogens and morphogen-stimulating agents described herein as therapeutic agents for protecting tissue from the tissue destructive effects associated with the body's inflammatory response; and 2) provide assays with which to test candidate morphogens and morphogen-stimulating agents for their efficacy.
I. USEFUL MORPHOGENS
As defined herein a protein is morphogenic if it is capable of inducing the developmental cascade of cellular and molecular events that culminate in the formation of new, organ-specific tissue and comprises at least the conserved C-terminal six cysteine skeleton or its functional equivalent (see supra). Specifically, the morphogens generally are capable of all of the following biological functions in a morphogenically permissive environment: stimulating proliferation of progenitor cells; stimulating the differentiation of progenitor cells; stimulating the proliferation of differentiated cells; and supporting the growth and maintenance of differentiated cells, including the "redifferentiation" of transformed cells. Details of how the morphogens useful in the method of this invention first were identified, as well as a description on how to make, use and test them for morphogenic activity are disclosed in U.S. Ser. No. 667,274, filed Mar. 11, 1991 and U.S. Ser. No. 752,764, filed Aug. 30, 1991, the disclosures of which are hereinabove incorporated by reference.
A candidate morphogen or morphogen composition can be evaluated for in vivo morphogenic utility generally according to the procedures set forth in U.S. Ser. No. 07/752,764. The proteins and compositions may be injected or surgically implanted in a mammal, following any of a number of procedures well known in the art. For example, surgical implant bioassays may be performed essentially following the procedure of Sampath et al. (1983) PNAS 80:6591-6595.
Histological sectioning and staining is preferred to determine the extent of morphogenesis in vivo, particularly in tissue repair procedures. Excised implants are fixed in Bouins Solution, embedded in paraffin, and cut into 6-8 .mu.m sections. Staining with toluidine blue or hemotoxylin/eosin demonstrates clearly the ultimate development of the new tissue. Twelve day implants are usually sufficient to determine whether the implants contain newly induced tissue.
Successful implants exhibit a controlled progression through the stages of induced tissue development allowing one to identify and follow the tissue-specific events that occur. For example, in endochondral bone formation the stages include:
(1) leukocytes on day one;
(2) mesenchymal cell migration and proliferation on days two and three;
(3) chondrocyte appearance on days five and six;
(4) cartilage matrix formation on day seven;
(5) cartilage calcification on day eight;
(6) vascular invasion, appearance of osteoblasts, and formation of new bone on days nine and ten;
(7) appearance of osteoblastic and bone remodeling and dissolution of the implanted matrix on days twelve to eighteen; and
(8) hematopoietic bone marrow differentiation in the ossicle on day twenty-one.
In addition to histological evaluation, biological markers may be used as a marker for tissue morphogenesis. Useful markers include tissue-specific enzymes whose activity may be assayed (e.g., spectrophotometrically) after homogenization of the implant. These assays may be useful for quantitation and for obtaining an estimate of tissue formation quickly after the implants are removed from the animal. For example, alkaline phosphatase activity may be used as a marker for osteogenesis.
Incorporation of systemically provided morphogens may be followed using tagged morphogens (e.g., radioactively labeled) and determining their localization in new tissue, and/or by monitoring their disappearance from the circulatory system using a standard pulse-chase labeling protocol. The morphogen also may be provided with a tissue-specific molecular tag, whose uptake may be monitored and correlated with the concentration of morphogen provided.
The morphogen to be assayed according to the above-described exemplary procedures can be purified from naturally-sourced material, or can be recombinantly produced from procaryotic or eucaryotic host cells, into which genetic material encoding a morphogen, e.g., genetic material bearing one of the nucleic acid sequences disclosed herein, has been introduced. Alternatively, the above-described exemplary procedures can be used to determine whether a novel protein suspected of being a morphogen indeed has morphogenic activity. Alternatively, novel morphogenic sequences may be identified following the procedures disclosed therein.
Particularly useful proteins include those which comprise the naturally derived sequences disclosed in Table II. Other useful sequences include biosynthetic constructs such as those disclosed in U.S. Pat. No. 5,011,691, the disclosure of which is incorporated herein by reference (e.g., COP-1, COP-3, COP-4, COP-5, COP-7, and COP-16).
Accordingly, the morphogens useful in the methods and compositions of this invention also may be described by morphogenically active proteins having amino acid sequences sharing 70% or, preferably, 80% homology (similarity) with any of the sequences described above, where "homology" is as defined herein above.
The morphogens useful in the method of this invention also can be described by any of the 6 generic sequences described herein (Generic Sequences 1, 2, 3, 4, 5 and 6). Generic sequences 1 and 2 also may include, at their N-terminus, the sequence
Cys Xaa Xaa Xaa Xaa (Seq. ID No. 15) 1 5
Table II, set forth below, compares the amino acid sequences of the active regions of native proteins that have been identified as morphogens, including human OP-1 (hOP-1, Seq. ID Nos. 5 and 16-17), mouse OP-1 (mOP-1, Seq. ID Nos. 6 and 18-19), human and mouse OP-2 (Seq. ID Nos. 7, 8, and 20-23), CBMP2A (Seq. ID No. 9), CBMP2B (Seq. ID No. 10), BMP3 (Seq. ID No. 26), DPP (from Drosophila, Seq. ID No. 11), Vgl, (from Xenopus, Seq. ID No. 12), Vgr-1 (from mouse, Seq. ID No. 13), GDF-1 (from mouse, Seq. ID Nos. 14, 32 and 33), 60A protein (from Drosophila, Seq. ID Nos. 24 and 25), BMP5 (Seq. ID No. 27) and BMP6 (Seq. ID No. 28). The sequences are aligned essentially following the method of Needleman et al. (1970) J. Mol. Biol., 48:443-453, calculated using the Align Program (DNAstar, Inc.) In the table, three dots indicates that the amino acid in that position is the same as the amino acid in hOP-1. Three dashes indicates that no amino acid is present in that position, and are included for purposes of illustrating homologies. For example, amino acid residue 60 of CBMP-2A and CBMP-2B is "missing". Of course, both these amino acid sequences in this region comprise Asn-Ser (residues 58, 59), with CBMP-2A then comprising Lys and Ile, whereas CBMP-2B comprises Ser and Ile.
TABLE II__________________________________________________________________________hOP-1 Cys Lys Lys His Glu Leu Tyr ValmOP-1 -- -- -- -- -- -- -- --hOP-2 -- Arg Arg -- -- -- -- --mOP-2 -- Arg Arg -- -- -- -- --DPP -- Arg Arg -- Ser -- -- --Vgl -- -- Lys Arg His -- -- --Vgr-1 -- -- -- -- Gly -- -- --CBMP-2A -- -- Arg -- Pro -- -- --CBMP-2B -- Arg Arg -- Ser -- -- --BMP3 -- Ala Arg Arg Tyr -- Lys --GDF-1 -- Arg Ala Arg Arg -- -- --60A -- Gln Met Glu Thr -- -- --BNP5 -- -- -- -- -- -- -- --BMP6 -- Arg -- -- -- -- -- --hOP-1 Ser Phe Arg Asp Leu Gly Trp Gln AspmOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- -- Gln -- -- -- -- Leu --mOP-2 Ser -- -- -- -- -- -- Leu --DPP Asp -- Ser -- Val -- -- Asp --Vgl Glu -- Lys -- Val -- -- -- AsnVgr-1 -- -- Gln -- Val -- -- -- --CBMP-2A Asp -- Ser -- Val -- -- Asn --CBMP-2B Asp -- Ser -- Val -- -- Asn --BMP3 Asp -- Ala -- Ile -- -- Ser GluGDF-1 -- -- -- Glu Val -- -- His Arg60A Asp -- Lys -- -- -- -- His --BMP5 -- -- -- -- -- -- -- -- --BMP6 -- -- Gln -- -- -- -- -- --hOP-1 Trp Ile Ile Ala Pro Glu Gly Tyr AlamOP-1 -- -- Gln -- -- -- -- -- --hOP-2 -- Val -- -- -- Gln -- -- SermOP-2 -- Val -- -- -- Gln -- -- SerDPP -- -- Val -- -- Leu -- -- AspVgl -- Val -- -- -- Gln -- -- MetVgr-1 -- -- -- -- -- Lys -- -- --CBMP-2A -- -- Val -- -- Pro -- -- HisCBMP-2B -- -- Val -- -- Pro -- -- GlnBMP3 -- -- -- Ser -- Lys Ser Phe AspGDF-1 -- Val -- -- -- Arg -- Phe Leu60A -- -- -- -- -- -- -- -- GlyBMP5 -- -- -- -- -- -- -- --BMP6 -- -- -- -- -- Lys -- --hOP-1 Ala Tyr Tyr Cys Glu Gly Glu Cys AlamOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- -- -- -- -- -- -- -- SermOP-2 -- -- -- -- -- -- -- -- --DPP -- -- -- -- His -- Lys -- ProVgl -- Asn -- -- Tyr -- -- -- ProVgr-1 -- Asn -- -- Asp -- -- -- SerCBMP-2A -- Phe -- -- His -- Glu -- ProCBMP-2B -- Phe -- -- His -- Asp -- ProBMP3 -- -- -- -- Ser -- Ala -- GlnGDF-1 -- Asn -- -- Gln -- Gln -- --60A -- Phe -- -- Ser 13 -- -- AsnBMP5 -- Phe -- -- Asp -- -- -- SerBMP6 -- Asn -- -- Asp -- -- -- SerhOP-1 Phe Pro Leu Asn Ser Tyr Met Asn AlamOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- -- -- Asp -- Cys -- -- --mOP-2 -- -- -- Asp -- Cys -- -- --DPP -- -- -- Ala Asp His Phe -- SerVgl Tyr -- -- Thr Glu Ile Leu -- GlyVgr-1 -- -- -- -- Ala His -- -- --CBMP-2A -- -- -- Ala Asp His Leu -- SerCBMP-2B -- -- -- Ala Asp His Leu -- SerGDF-1 Leu -- Val Ala Leu Ser Gly Ser** --BMP3 -- -- Met Pro Lys Ser Leu Lys Pro60A -- -- -- -- Ala His -- -- --BMP5 -- -- -- -- Ala His Met -- --BMP6 -- -- -- -- Ala His Met -- --hOP-1 Thr Asn His Ala Ile Val Gln Thr LeumOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- -- -- -- -- Leu -- Ser --mOP-2 -- -- -- -- -- Leu -- Ser --DPP -- -- -- -- Val -- -- -- --Vgl Ser -- -- -- -- Leu -- -- --Vgr-1 -- -- -- -- -- -- -- -- --CBMP-2A -- -- -- -- -- -- -- -- --CBMP-2B -- -- -- -- -- -- -- -- --BMP3 Ser -- -- -- Thr Ile -- Ser IleGDF-1 Leu -- -- -- Val Leu Arg Ala --60A -- -- -- -- -- -- -- -- --BMP5 -- -- -- -- -- -- -- -- --BMP6 -- -- -- -- -- -- -- -- --hOP-1 Val His Phe Ile Asn Pro Glu Thr ValmOP-1 -- -- -- -- -- -- Asp -- --hOP-2 -- His Leu Met Lys -- Asn Ala --mOP-2 -- His Leu Met Lys -- Asp Val --DPP -- Asn Asn Asn -- -- Gly Lys --Vgl -- -- Ser -- Glu -- -- Asp IleVgr-1 -- -- Val Met -- -- -- Tyr --CBMP-2A -- Asn Ser Val -- Ser -- Lys IleCBMP-2B -- Asn Ser Val -- Ser -- Ser IleBMP3 -- Arg Ala** Gly Val Val Pro Gly IleGDF-1 Met -- Ala Ala Ala -- Gly Ala Ala60A -- -- Leu Leu Glu -- Lys Lys --BMP5 -- -- Leu Met Phe -- Asp His --BMP6 -- -- Leu Met -- -- -- Tyr --hOP-1 Pro Lys Pro Cys Cys Ala Pro Thr GlnmOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- -- Ala -- -- -- -- -- LysmOP-2 -- -- Ala -- -- -- -- -- LysDPP -- -- Ala -- -- Val -- -- --Vgl -- Leu -- -- -- Val -- -- LysVgr-1 -- -- -- -- -- -- -- -- LysCBMP-2A -- -- Ala -- -- Val -- -- GluCBMP-2B -- -- Ala -- -- Val -- -- GluBMP3 -- Glu -- -- -- Val -- Glu LysGDF-1 Asp Leu -- -- -- Val -- Ala Arg60A -- -- -- -- -- -- -- -- ArgBMP5 -- -- -- -- -- -- -- -- LysBMP6 -- -- -- -- -- -- -- -- LyshOP-1 Leu Asn Ala Ile Ser Val Leu Tyr PhemOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- Ser -- Thr -- -- -- -- TyrmOP-2 -- Ser -- Thr -- -- -- -- TyrVgl Met Ser Pro -- -- Met -- Phe TyrVgr-1 Val -- -- -- -- -- -- -- --DPP -- Asp Ser Val Ala Met -- -- LeuCBMP-2A -- Ser -- -- -- Met -- -- LeuCBMP-2B -- Ser -- -- -- Met -- -- LeuBMP3 Met Ser Ser Leu -- Ile -- Phe TyrGDF-1 -- Ser Pro -- -- -- -- Phe --60A -- Gly -- Leu Pro -- -- -- HisBMP5 -- -- -- -- -- -- -- -- --BMP6 -- -- -- -- -- -- -- -- --hOP-1 Asp Asp Ser Ser Asn Val Ile Leu LysmOP-1 -- -- -- -- -- -- -- -- --hOP-2 -- Ser -- Asn -- -- -- -- ArgmOP-2 -- Ser -- Asn -- -- -- -- ArgDPP Asn -- Gln -- Thr -- Val -- --Vgl -- Asn Asn Asp -- -- Val -- ArgVgr-1 -- -- Asn -- -- -- -- -- --CBMP-2A -- Glu Asn Glu Lys -- Val -- --CBMP-2B -- Glu Tyr Asp Lys -- Val -- --BMP3 -- Glu Asn Lys -- -- Val -- --GDF-1 -- Asn -- Asp -- -- Val -- Arg60A Leu Asn Asp Glu -- -- Asn -- --BMP5 -- -- -- -- -- -- -- -- --BMP6 -- -- Asn -- -- -- -- -- --hOP-1 Lys Tyr Arg Asn Met Val Val ArgmOP-1 -- -- -- -- -- -- -- --hOP-2 -- His -- -- -- -- -- LysmOP-2 -- His -- -- -- -- -- LysDPP Asn -- Gln Glu -- Thr -- ValVgl His -- Glu -- -- Ala -- AspVgr-1 -- -- -- -- -- -- -- --CBMP-2A Asn -- Gln Asp -- -- -- GluCBMP-2B Asn -- Gln Glu -- -- -- GluBMP3 Val -- Pro -- -- Thr -- GluGDF-1 Gln -- Glu Asp -- -- -- Asp60A -- -- -- -- -- Ile -- LysBMP5 -- -- -- -- -- -- -- --BMP6 -- -- -- Trp -- -- -- --hOP-1 Ala Cys Gly Cys HismOP-1 -- -- -- -- --hOP-2 -- -- -- -- --mOP-2 -- -- -- -- --DPP Gly -- -- -- ArgVgl Glu -- -- -- ArgVgr-1 -- -- -- -- --CBMP-2A Gly -- -- -- ArgCBMP-2B Gly -- -- -- ArgBMP3 Ser -- Ala -- ArgGDF-1 Glu -- -- -- Arg60A Ser -- -- -- --BMP5 Ser -- -- -- --BMP6 -- -- -- -- --__________________________________________________________________________ **Between residues 56 and 57 of BMP3 is a Val residue; between residues 4 and 44 of GDF1 lies the amino acid sequence GlyGly-Pro-Pro.
As is apparent from the foregoing amino acid sequence comparisons, significant amino acid changes can be made within the generic sequences while retaining the morphogenic activity. For example, while the GDF-1 protein sequence depicted in Table II shares only about 50% amino acid identity with the hOP1sequence described therein, the GDF-1 sequence shares greater than 70% amino acid sequence homology (or "similarity") with the hOP1 sequence, where "homology" or "similarity" includes allowed conservative amino acid changes within the sequence as defined by Dayoff, et al., Atlas of Protein Sequence and Structure vol.5, supp.3, pp.345-362, (M. O. Dayoff, ed., Nat'l BioMed. Res. Fd'n, Washington D.C. 1979.)
The currently most preferred protein sequences useful as morphogens in this invention include those having greater than 60% identity, preferably greater than 65% identity, with the amino acid sequence defining the conserved six cysteine skeleton of hOP1 (e.g., residues 43-139 of Seq. ID No. 5). These most preferred sequences include both allelic and species variants of the OP-1 and OP-2 proteins, including the Drosophila 60A protein. Accordingly, in still another preferred aspect, the invention includes morphogens comprising species of polypeptide chains having the generic amino acid sequence referred to herein as "OPX", which defines the seven cysteine skeleton and accommodates the identities between the various identified mouse and human OP1 and OP2 proteins. OPX is presented in Seq. ID No. 29. As described therein, each Xaa at a given position independently is selected from the residues occurring at the corresponding position in the C-terminal sequence of mouse or human OP1 or OP2 (see Seq. ID Nos. 5-8 and/or Seq. ID Nos. 16-23).
II. FORMULATIONS AND METHODS FOR ADMINISTERING THERAPEUTIC AGENTS
The morphogens may be provided to an individual by any suitable means, preferably directly (e.g., locally, as by injection or topical administration to a tissue locus) or systemically (e.g., parenterally or orally). Where the morphogen is to be provided parenterally, such as by intravenous, subcutaneous, intramuscular, intraorbital, ophthalmic, intraventricular, intracranial, intracapsular, intraspinal, intracisternal, intraperitoneal, buccal, rectal, vaginal, intranasal or by aerosol administration, the morphogen preferably comprises part of an aqueous solution. The solution is physiologically acceptable so that in addition to delivery of the desired morphogen to the patient, the solution does not otherwise adversely affect the patient's electrolyte and volume balance. The aqueous medium for the morphogen thus may comprise normal physiologic saline (9.85% NaCl, 0.15M), pH 7-7.4. The aqueous solution containing the morphogen can be made, for example, by dissolving the protein in 50% ethanol containing acetonitrile in 0.1% trifluoroacetic acid (TFA) or 0.1% HC1, or equivalent solvents. One volume of the resultant solution then is added, for example, to ten volumes of phosphate buffered saline (PBS), which further may include 0.1-0.2% human serum albumin (HSA). The resultant solution preferably is vortexed extensively. If desired, a given morphogen may be made more soluble by association with a suitable molecule. For example, association of the mature dimer with the pro domain of the morphogen keeps the morphogen soluble in physiological buffers. In fact, the endogenous protein is thought to be transported in this form. Another molecule capable of enhancing solubility and particularly useful for oral administrations, is casein. For example, addition of 0.2% casein increases solubility of the mature active form of OP-1 by 80%. Other components found in milk and/or various serum proteins also may be useful.
Useful solutions for parenteral administration may be prepared by any of the methods well known in the pharmaceutical art, described, for example, in Remington's Pharmaceutical Sciences (Gennaro, A., ed.), Mack Pub., 1990. Formulations may include, for example, polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, hydrogenated naphthalenes, and the like. Formulations for direct administration, in particular, may include glycerol and other compositions of high viscosity to help maintain the morphogen at the desired locus. Biocompatible, preferably bioresorbable, polymers, including, for example, hyaluronic acid, collagen, tricalcium phosphate, polybutyrate, lactide, and glycolide polymers and lactide/glycolide copolymers, may be useful excipients to control the release of the morphogen in vivo. Other potentially useful parenteral delivery systems for these morphogens include ethylene-vinyl acetate copolymer particles, osmotic pumps, implantable infusion systems, and liposomes. Formulations for inhalation administration contain as excipients, for example, lactose, or may be aqueous solutions containing, for example, polyoxyethylene-9-lauryl ether, glycocholate and deoxycholate, or oily solutions for administration in the form of nasal drops, or as a gel to be applied intranasally. Formulations for parenteral administration may also include glycocholate for buccal administration, methoxysalicylate for rectal administration, or cutric acid for vaginal administration.
Suppositories for rectal administration also may be prepared by mixing the morphogen or morphogen-stimulating agent with a non-irritating excipient such as cocoa butter or other compositions which are solid at room temperature and liquid at body temperatures.
Formulations for topical administration to the skin surface may be prepared by dispersing the morphogen or morphogen-stimulating agent with a dermatologically acceptable carrier such as a lotion, cream, ointment or soap. Particularly useful are carriers capable of forming a film or layer over the skin to localize application and inhibit removal. For topical administration to internal tissue surfaces, the morphogen may be dispersed in a liquid tissue adhesive or other substance known to enhance adsorption to a tissue surface. For example, hydroxypropylcellulose or fibrinogen/thrombin solutions may be used to advantage. Alternatively, tissue-coating solutions, such as pectin-containing formulations may be used.
Alternatively, the morphogens described herein may be administered orally. Oral administration of proteins as therapeutics generally is not practiced as most proteins are readily degraded by digestive enzymes and acids in the mammalian digestive system before they can be absorbed into the bloodstream. However, the morphogens described herein typically are acid stable and protease-resistant (see, for example, U.S. Pat. No. 4,968,590.) In addition, at least one morphogen, OP-1, has been identified in mammary gland extract, colostrum and 57-day milk. Moreover, the OP-1 purified from mammary gland extract is morphogenically active. Specifically, this protein induces endochondral bone formation in mammals when implanted subcutaneously in association with a suitable matrix material, using a standard in vivo bone assay, such as is disclosed in U.S. Pat. No. 4,968,590. Moreover, the morphogen also is detected in the bloodstream. Finally, soluble form morphogen, e.g., mature morphogen associated with the pro domain, is morphogenically active. These findings indicate that oral and parenteral administration are viable means for administering morphogens to an individual. In addition, while the mature forms of certain morphogens described herein typically are sparingly soluble, the morphogen form found in milk (and mammary gland extract and colostrum) is readily soluble, probably by association of the mature, morphogenically active form with part or all of the pro domain of the intact sequence and/or by association with one or more milk components. Accordingly, the compounds provided herein also may be associated with molecules capable of enhancing their solubility in vitro or in vivo.
The compounds provided herein also may be associated with molecules capable of targeting the morphogen or morphogen-stimulating agent to the desired tissue. For example, an antibody, antibody fragment, or other binding protein that interacts specifically with a surface molecule on cells of the desired tissue, may be used. Useful targeting molecules may be designed, for example, using the single chain binding site technology disclosed, for example, in U.S. Pat. No. 5,091,513.
As described above, the morphogens provided herein share significant sequence homology in the C-terminal active domains. By contrast, the sequences typically diverge significantly in the sequences which define the pro domain. Accordingly, the pro domain is thought to be morphogen-specific. As described above, it is also known that the various morphogens identified to date are differentially expressed in the different tissues. Accordingly, without being limited to any given theory, it is likely that, under natural conditions in the body, selected morphogens typically act on a given tissue. Accordingly, part or all of the pro domains which have been identified associated with the active form of the morphogen in solution, may serve as targeting molecules for the morphogens described herein. For example, the pro domains may interact specifically with one or more molecules at the target tissue to direct the morphogen associated with the pro domain to that tissue. Accordingly, another useful targeting molecule for targeting morphogen to a tissue of interest is part or all of a morphogen pro domain. For example, part or all of the pro domain of GDF-1, may be used to target a morphogen to nerve tissue. Alternatively, part or all of the pro domains of OP-1 or CBMP2 may be used to target a morphogen to bone tissue, both of which proteins are found naturally associated with bone tissue.
The morphogens described herein are useful for providing neuroprotective effects to alleviate neural pathway damage associated with the body's immune/inflammatory response to an initial injury to nerve tissue. As used herein, a "neural pathway" describes a nerve circuit for the passage of electric signals from a source to a target cell site and includes both the central nervous system (CNS) and peripheral nervous system (PNS). The pathway includes the neurons through which the electric impulse is transported, including groups of interconnecting neurons, the nerve fibers formed by bundled neuronal axons, and the glial cells surrounding and associated with the neurons. An inflammatory response to nerve tissue injury may follow trauma to nerve tissue, caused, for example, by an autoimmune (including autoantibody) dysfunction, neoplastic lesion, infection, chemical or mechanical trauma, or other disease. An exemplary nerve-related inflammatory disease is multiple sclerosis. Neural pathway damage also can result from a reduction or interruption, e.g., occlusion, of a neural blood supply, as in an embolic stroke, (e.g, ischemia or hypoxia-induced injury), or by other trauma to the nerve or surrounding material. In addition, at least part of the damage associated with a number of primary brain tumors also appears to be immunologically related. Application of the morphogen directly to the cells to be treated, or providing the morphogen to the mammal systemically, for example, intravenously or indirectly by oral administration, may be used to alleviate and/or inhibit the immunologically related response to a neural injury. Alternatively, administration of an agent capable of stimulating morphogen expression and/or secretion in vivo, preferably at the site of injury, also may be used. Where the injury is to be induced, as during surgery or other aggressive clinical treatment, the morphogen or agent may be provided prior to induction of the injury to provide a neuroprotective effect to the nerve tissue at risk.
Where the morphogen is intended for use as a therapeutic to alleviate tissue damage associated with an immune/inflammatory condition of the central nervous system (CNS) an additional problem must be addressed: overcoming the so-called "blood-brain barrier", the brain capillary wall structure that effectively screens out all but selected categories of molecules present in the blood, preventing their passage into the brain. The blood-brain barrier may be bypassed effectively by direct infusion of the morphogen or morphogen-stimulating agent into the brain. Alternatively, the morphogen or morphogen-stimulating agent may be modified to enhance its transport across the blood-brain barrier. For example, truncated forms of the morphogen or a morphogen-stimulating agent may be most successful. Alternatively, the morphogen or morphogen-stimulating agent may be modified to render it more lipophilic, or it may be conjugated to another molecule which is naturally transported across the barrier, using standard means known to those skilled in the art, as, for example, described in Pardridge, Endocrine Reviews: 7:314-330 (1986) and U.S. Pat. No. 4,801,575. A more detailed description of morphogens for use in treating inflammatory conditions in nerve tissue, including a model for evaluating morphogen transport across the blood brain barrier is disclosed in U.S. Ser. No. 922,813, the disclosure of which is incorporated herein by reference.
Finally, the morphogens or morphogen-stimulating agents provided herein may be administered alone or in combination with other molecules known to be beneficial in the treatment compositions and methods described herein, including, but not limited to anticoagulants, free oxygen radical inhibiting agents, salicylic acid, vitamin D, and other antiinflammatory agents. Psoriais treatments also may include ultra-violet light treatment, zinc oxide and retinoids.
The compounds provided herein can be formulated into pharmaceutical compositions by admixture with pharmaceutically acceptable nontoxic excipients and carriers. As noted above, such compositions may be prepared for parenteral administration, particularly in the form of liquid solutions or suspensions; for oral administration, particularly in the form of tablets or capsules; or intranasally, particularly in the form of powders, nasal drops, or aerosols.
The compositions can be formulated for parenteral or oral administration to humans or other mammals in therapeutically effective amounts, e.g., amounts which provide appropriate concentrations for a time sufficient to alleivate the tissue destructive effects associated with the inflammatory response, including protecting tissue in anticipation of tissue damage.
As will be appreciated by those skilled in the art, the concentration of the compounds described in a therapeutic composition will vary depending upon a number of factors, including the dosage of the drug to be administered, the chemical characteristics (e.g., hydrophobicity) of the compounds employed, and the route of administration. The preferred dosage of drug to be administered also is likely to depend on such variables as the type and extent of progression of the tissue damage, the overall health status of the particular patient, the relative biological efficacy of the compound selected, the formulation of the compound excipients, and its route of administration. In general terms, the compounds of this invention may be provided in an aqueous physiological buffer solution containing about 0.001% to 10% w/v compound for parenteral administration. Typical dose ranges are from about 10 ng/kg to about 1 g/kg of body weight per day; a preferred dose range is from about 0.1 .mu.g/kg to 100 mg/kg of body weight per day. Optimally, the morphogen dosage given in most cases is between 0.1-100 .mu.g of protein per kilogram weight of the patient. No obvious morphogen induced pathological lesions are induced when mature morphogen (e.g., OP-i, 20 .mu.g) is administered daily to normal growing rats for 21 consecutive days. Moreover, 10 .mu.g systemic injections of morphogen (e.g., OP-1) injected daily for 10 days into normal newborn mice does not produce any gross abnormalities.
In administering morphogens systemically in the methods of the present invention, preferably a large volume loading dose is used at the start of the treatment. The treatment then is continued with a maintenance dose. Further administration then can be determined by monitoring at intervals the levels of the morphogen in the blood.
Where tissue injury is induced deliberately as part of, for example, a surgical procedure, the morphogen preferably is provided just prior to, or concomitant with induction of the trauma. Preferably, the morphogen is administered prophylactically in a surgical setting.
Alternatively, an effective amount of an agent capable of stimulating endogenous morphogen levels may be administered by any of the routes described above. For example, an agent capable of stimulating morphogen production and/or secretion from cells of affected tissue or a transplanted organ may be provided to a mammal, e.g., by direct administration of the morphogen to the tissue or organ. A method for identifying and testing agents capable of modulating the levels of endogenous morphogens in a given tissue is described generally herein in Example 15, and in detail in copending U.S. Ser. No. 752,859, filed Aug. 30, 1991, the disclosure of which is incorporated herein by reference. Briefly, candidate compounds can be identified and tested by incubating the compound in vitro with a test tissue or cells thereof, for a time sufficient to allow the compound to affect the production, i.e., the expression and/or secretion, of a morphogen produced by the cells of that tissue.
For purposes of the present invention, the above-described morphogens effective in alleviating ischemic-reperfusion injury (or the agents that stimulate them, referred to herein collectively as "therapeutic agent") are administered prior to or during the restoration of oxygen (e.g., restoration of blood flow, reperfusion.) Where treatment is to follow an existing injury, the therapeutic agent preferably is administered as an intravenous infusion provided acutely after the hypoxic or ischemic condition occurs. For example, the therapeutic agent can be administered by intravenous infusion immediately after a cerebral infarction, a myocardial infarction, asphyxia, or a cardiopulmonary arrest. Where ischemia or hypoxia is deliberately induced as part of, for example, a surgical procedure where circulation to an organ or organ system is deliberately and/or transiently interrupted, e.g., in carotid enterectomy, coronary artery bypass, grafting, organ transplanting, fibrinolytic therapy, etc., the therapeutic agent preferably is provided just prior to, or concomitant with, reduction of oxygen to the tissue. Preferably, the therapeutic agent is administered prophylactically in a surgical setting.
Similarly, where hyperoxia induced-injury already has occurred, the morphogen is administered upon diagnosis. Where hyperoxia may be induced as, for example, during treatment of prematurely newborn babies, or patients suffering from pulmonary diseases such as emphysema, the therapeutic agent preferably is administered prior to administration of oxygen (e.g., prophylactically).

III. EXAMPLES
Example 1
Identification of Morphogen-Expressing Tissue
Determining the tissue distribution of morphogens may be used to identify different morphogens expressed in a given tissue, as well as to identify new, related morphogens. Tissue distribution also may be used to identify useful morphogen-producing tissue for use in screening and identifying candidate morphogen-stimulating agents. The morphogens (or their mRNA transcripts) readily are identified in different tissues using standard methodologies and minor modifications thereof in tissues where expression may be low. For example, protein distribution may be determined using standard Western blot analysis or immunofluorescent techniques, and antibodies specific to the morphogen or morphogens of interest. Similarly, the distribution of morphogen transcripts may be determined using standard Northern hybridization protocols and transcript-specific probes.
Any probe capable of hybridizing specifically to a transcript, and distinguishing the transcript of interest from other, related transcripts may be used. Because the morphogens described herein share such high sequence homology in their active, C-terminal domains, the tissue distribution of a specific morphogen transcript may best be determined using a probe specific for the pro region of the immature protein and/or the N-terminal region of the mature protein. Another useful sequence is the 3' non-coding region flanking and immediately following the stop codon. These portions of the sequence vary substantially among the morphogens of this invention, and accordingly, are specific for each protein. For example, a particularly useful Vgr-1-specific probe sequence is the PvuII-SacI fragment, a 265 bp fragment encoding both a portion of the untranslated pro region and the N-terminus of the mature sequence (see Lyons et al. (1989) PNAS 86:4554-4558 for a description of the cDNA sequence). Similarly, particularly useful mOP-1-specific probe sequences are the BstX1-BglI fragment, a 0.68 Kb sequence that covers approximately two-thirds of the mOP-1 pro region; a StuI--StuI fragment, a 0.2 Kb sequence immediately upstream of the 7-cysteine domain; and the Earl-Pst1 fragment, an 0.3 Kb fragment containing a portion of the 3'untranslated sequence (See Seq. ID No. 18, where the pro region is defined essentially by residues 30-291.) Similar approaches may be used, for example, with hOP-1 (Seq. ID No. 16) or human or mouse OP-2 (Seq. ID Nos. 20 and 22.)
Using these morphogen-specific probes, which may be synthetically engineered or obtained from cloned sequences, morphogen transcripts can be identified in mammalian tissue, using standard methodologies well known to those having ordinary skill in the art. Briefly, total RNA is prepared from various adult murine tissues (e.g., liver, kidney, testis, heart, brain, thymus and stomach) by a standard methodology such as by the method of Chomczyaski et al. ((1987) Anal. Biochem 162:156-159) and described below. Poly (A)+RNA is prepared by using oligo (dT)-cellulose chromatography (e.g., Type 7, from Pharmacia LKB Biotechnology, Inc.). Poly (A)+ RNA (generally 15 pg) from each tissue is fractionated on a 1% agarose/formaldehyde gel and transferred onto a Nytran membrane (Schleicher & Schuell). Following the transfer, the membrane is baked at 80.degree. C. and the RNA is cross-linked under UV light (generally 30 seconds at 1 mW/cm.sup.2). Prior to hybridization, the appropriate probe is denatured by heating. The hybridization is carried out in a lucite cylinder rotating in a roller bottle apparatus at approximately 1 rev/min for approximately 15 hours at 37.degree. C. using a hybridization mix of 40% formamide, 5.times. Denhardts, 5.times. SSPE, and 0.1% SDS. Following hybridization, the non-specific counts are washed off the filters in 0.1.times. SSPE, 0.1% SDS at 50.degree. C.
Examples demonstrating the tissue distribution of various morphogens, including Vgr-1, OP-1, BMP2, BMP3, BMP4, BMP5, GDF-1, and OP-2 in developing and adult tissue are disclosed in co-pending U.S. Ser. No. 752,764, and in Ozkaynak, et al., (1991) Biochem. Biophys. Res. Commn. 179:116-123, and Ozkaynak, et al. (1992) (JBC, in press), the disclosures of which are incorporated herein by reference. Using the general probing methodology described herein, northern blot hybridizations using probes specific for these morphogens to probe brain, spleen, lung, heart, liver and kidney tissue indicate that kidney-related tissue appears to be the primary expression source for OP-1, with brain, heart and lung tissues being secondary sources. OP-1 RNA also was identified in salivary glands, specifically rat parotid glands, using this probing methodology. Lung tissue appears to be the primary tissue expression source for Vgr-1, BMP5, BMP4 and BMP3. Lower levels of Vgr-1 also are seen in kidney and heart tissue, while the liver appears to be a secondary expression source for BMP5, and the spleen appears to be a secondary expression source for BMP4. GDF-1 appears to be expressed primarily in brain tissue. To date, OP-2 appears to be expressed primarily in early embryonic tissue. Specifically, northern blots of murine embryos and 6-day post-natal animals shows abundant OP2 expression in 8-day embryos. Expression is reduced significantly in 17-day embryos and is not detected in post-natal animals.
Example 2
Active Morphogens in Body Fluids
OP-1 expression has been identified in saliva (specifically, the rat parotid gland, see Example 1), human blood serum, and various milk forms, including mammary gland extract, colostrum, and 57-day bovine milk. Moreover, and as described in U.S. Ser. No. 923,780, the disclosure of which is incorporated herein by reference, the body fluid-extracted protein is morphogenically active. The discovery that the morphogen naturally is present in milk and saliva, together with the known observation that mature, active OP-1 is acid-stable and protease-resistant, indicate that oral administration is a useful route for therapeutic administration of morphogen to a mammal. Oral administration typically is the preferred mode of delivery for extended or prophylactic therapies. In addition, the identification of morphogen in all milk forms, including colostrum, suggests that the protein may play a significant role in tissue development, including skeletal development, of juveniles.
2.1 Morphogen Detection in Milk
OP-1 was partially purified from rat mammary gland extract and bovine colostrum and 57 day milk by passing these fluids over a series of chromatography columns: (e.g., cation-exchange, affinity and reverse phase). At each step the eluant was collected in fractions and these were tested for the presence of OP-1 by standard immunoblot. Immunoreactive fractions then were combined and purified further. The final, partially purified product then was examined for the presence of OP-1 by Western blot analysis using OP-1-specific antisera, and tested for in vivo and in vitro activity.
OP-1 purified from the different milk sources were characterized by Western blotting using antibodies raised against OP-1 and BMP2. Antibodies were prepared using standard immunology protocols well known in the art, and as described generally in Example 15, below, using full-length E. coli-produced OP-1 and BMP2 as the immunogens. In all cases, the purified OP-1 reacted only with the anti-OP-1 antibody, and not with anti-BMP2 antibody.
The morphogenic activity of OP-1 purified from mammary gland extract was evaluated in vivo essentially following the rat model assay described in U.S. Pat. No. 4,968,590, hereby incorporated by reference. Briefly, a sample was prepared from each OP-1 immunoreactive fraction of the mammary gland extract-derived OP-1 final product by lyophilizing a portion (33%) of the fraction and resuspending the protein in 220 .mu.l of 50% acetonitrile/0.1% TFA. After vortexing, 25 mg of collagen matrix was added. The samples were lyophilized overnight, and implanted in Long Evans rats (Charles River Laboratories, Wilmington, Mass., 28-35 days old). Each fraction was implanted in duplicate. For details of the collagen matrix implantation procedure, see, for example, U.S. Pat. No. 4,968,590, hereby incorporated by reference. After 12 days, the implants were removed and evaluated for new bone formation by histological observation as described in U.S. Pat. No. 4,968,590. In all cases, the immunoreactive fractions were osteogenically active.
2.2 Morphogen Detection in Serum
Morphogen may be detected in serum using morphogen-specific antibodies. The assay may be performed using any standard immunoassay, such as Western blot (immunoblot) and the like. Preferably, the assay is performed using an affinity column to which the morphogen-specific antibody is bound and through which the sample serum then is poured, to selectively extract the morphogen of interest. The morphogen then is eluted. A suitable elution buffer may be determined empirically by determining appropriate binding and elution conditions first with a control (e.g., purified, recombinantly-produced morphogen.) Fractions then are tested for the presence of the morphogen by standard immunoblot, and the results confirmed by N-terminal sequencing. Preferably, the affinity column is prepared using monoclonal antibodies. Morphogen concentrations in serum or other fluid samples then may be determined using standard protein quantification techniques, including by spectrophotometric absorbance or by quantitation of conjugated antibody.
Presented below is a sample protocol for identifying OP-1 in serum. Following this general methodology other morphogens may be detected in body fluids, including serum. The identification of morphogen in serum further indicates that systemic administration is a suitable means for providing therapeutic concentrations of a morphogen to an individual, and that morphogens likely behave systemically as endocrine-like factors. Finally, using this protocol, fluctuations in endogenous morphogen levels can be detected, and these altered levels may be used as an indicator of tissue dysfunction. Alternatively, fluctuations in morphogen levels may be assessed by monitoring morphogen transcription levels, either by standard northern blot analysis as described in Example 1, or by in situ hybridization, using a labelled probe capable of hybridizing specifically to morphogen "mRNA", and standard RNA hybridization protocols well described in the art and described generally in Example 1.
OP-1 was detected in human serum using the following assay. A monoclonal antibody raised against mammalian, recombinantly produced OP-1 using standard immunology techniques well described in the art and described generally in Example 15, was immobilized by passing the antibody over an aqarose-activated gel (e.g., Affi-Gel.TM., from Bio-Rad Laboratories, Richmond, Calif., prepared following manufacturer's instructions) and used to purify OP-1 from serum. Human serum then was passed over the column and eluted with 3M K-thiocyanate. K-thiocyanante fractions then were dialyzed in 6M urea, 20 mM PO.sub.4, pH 7.0, applied to a C8 HPLC column, and eluted with a 20 minute, 25-50% acetonitrile/0.1% TFA gradient. Mature, recombinantly produced OP-1 homodimers elute between 20-22 minutes. Fractions then were collected and tested for the presence of OP-1 by standard immunoblot using an OP-1 specific antibody as for Example 2.A.
Administered or endogenous morphogen levels may be monitored in the therapies described herein by comparing the quantity of morphogen present in a body fluid sample with a predetermined reference value, for example, to evaluate the efficiency of a therapeutic protocol, and the like. In addition, fluctuations in the level of endogenous morphogen antibodies may be detected by this method, most likely in serum, using an antibody or other binding protein capable of interacting specifically with the endogenous morphogen antibody. Detected fluctuations in the levels of the morphogen or endogenous antibody may be used, for example, as indicators of a change in tissue status. For example, as damaged tissue is regenerated and the tissue or organ's function returns to "normal" and, in the absence of additional tissue damage, lower doses of morphogen may be required, and a higher level of circulating morphogen antibody may be measured.
Example 3
Effect of Morphogen after the Onset of the Ischemic Process
The cardioprotective effect of morphogens following ischemic-reperfusion injury in a mammal can readily be assessed in a rat model. In this example, morphogen (e.g., OP-1) is administered just prior to the onset of the ischemic process in experimentally-induced myocardial infracted rats, essentially following the method of Lefer, et al. (1990) Science 249:61-64 and (1992) J. Mol. Cell. Cardiol. 24: 385-393, the disclosures of which are hereby incorporated by reference. Briefly, loss of myocardial tissue function following ischemia and reperfusion is assayed by measuring loss of myocardial creatine kinease activity (CK) and loss of endothelium-dependent vasorelaxation function (see Example 4, below).
In a first group of ether-anesthetized rats, the left coronary artery was occluded just proximal to the first main branch with a silk ligature to induce a myocardial infarction (MI). The ligature was removed 10 minutes after occlusion to allow for coronary reperfusion. This first group is referred to herein as the "myocardial infarcted" (MI) group. A second group of rats underwent the same procedure except that the coronary artery was not occluded, and thus no myocardial infarction occurred. The second group of rats is referred to herein as the "sham myocardial infarcted group" (SHAM MI).
The first group of rats, the MI group of rats, further was divided into three sup-groups. 2 .mu.g of morphogen (OP-1) were injected intravenously into the first sub-group of MI rats 10 minutes after ligature, immediately before reperfusion; into the second sub-group of MI rats 20 .mu.g of OP-1 were injected intravenously 10 minutes after ligature and immediately before reperfusion; and into the third sub-group of MI rats (control) was injected vehicle only, e.g., 0.9% NaCl, as for the OP-1 treated rats.
Twenty-four hours later, the hearts were removed from all of the rats and the levels of creatine kinase (CK) from the left ventricle (the infarcted region) and from the interventricular septum (the control nonischemic region) were determined by standard means. By comparing the difference in CK activities in both regions, the amount of CK activity lost from the infarcted region was used as an index of cardiac cellular injury to the infarcted region.
As shown in FIG. 1, the data indicate that morphogens (e.g., OP-1) can provide significant cardioprotective effect when provided to ischemic tissue. In the figure, CK loss is graphed as the difference in specific CK activity between the interventricular septum and the left ventricle.
The loss of CK activity by the subgroup of MI rats which received 2 .mu.g of OP-1 just before reperfusion showed some protection as compared with the control MI rats which received injections of vehicle alone, when the levels from both subgroups are measured against, and compared to, the levels obtained for the SHAM MI control. Significant cardioprotection was observed in the subgroup of MI rats which received 20 .mu.g of OP-1 immediately before reperfusion as compared with the control MI rats which received injections of vehicle alone, when the levels from both subgroups are measured against, and compared to, the levels contained within the SHAM MI control.
These data indicate that OP-1 offers significant cardiac protection when administered after ischemia and before reperfusion.
A variation of this example also may be performed providing morphogen to the animal prior to induction of ischemia. The experiments may be performed both in normal and immune-compromised rats to assess the cardioprotective effects of morphogen administered prior to ischemia.
Example 4
Vasodilation of Myocardial Infarcted Cardiac Tissue Treated with Morphogen
Certain vasodilators like acetylcholine (ACh) and adenosine diphosphate (ADP, an immune mediator) exert their vasodilation activity only in the presence of intact endothelium, which is stimulated to release a substance termed endothelium-derived relaxing factor (EDRF). If the endothelium is injured so that EDRF is not released, no vasodilation occurs in response to these endothelium-dependent agents. In contrast, several other vasodilators including nitroglycerine (NTG) and nitroprusside, are endothelium-independent dilators, as they dilate blood vessels directly.
The present example demonstrates the ability of OP-1 to prevent the loss of cardioendothelium-dependent relaxation (EDR) activity in the coronary microvasculature following reperfusion of ischemic myocardium, and their ability to reduce myocardial injury 24 hours after morphogen treatment. Briefly, 2 or 24 hours after morphogen treatment ischemia-reperfusion injury is induced in isolated rat hearts, the reperfused hearts are are vasodilated with either ACh or NTG. In the absence of morphogen treatment, injured tissue should inhibit ACh-induced vasodilation, but not NTG-induced vasodilation. Morphogen treatment in expected to enhance ACh-induced vasodilation in the reperfused hearts.
Accordingly, 48 adult male Sprague-Dawley rats (250-330 g) were divided into eight groups of 6 rats each. Twelve rats were subjected to sham myocardial infarcts (SHAM MI) as described in Example 3. The hearts of the remaining 36 rats were isolated as follows: one set of twelve rats was injected intravenously with OP-1 24 hours prior to isolation of the heart; another set of rats was injected intravenously with 20 .mu.g of OP-1 2 hours prior to isolation of the heart; the final group of rats was injected with vehicle only (e.g., 0.9% NaCl.). The rats then were anesthetized with pentobarbital sodium (35 mg/kg, intraperitonial); their hearts were isolated and perfused by the Langendorff method at a constant flow (15 ml/min) with oxygenated Krebs-Henseleit solution (Aoki et al. (1988) J. Pharmacol. 95:35).
Each group of rats then were divided into two subgroups of six rats each. Twenty minutes before reperfusion, coronary vasodilator response was measured by inducing constriction with 0.05 .mu.mol U-44619 (9,11-methanoepoxyprostaglandin H.sub.2) followed by a vasodilating agent 3 minutes later: subgroup one 3-15 nmol ACh; subgroup 2-15 nmol NTG and the increase in coronary perfusion pressure (CPP) level measured as an indication of vasodilation. When CPP levels returned to normal, the hearts were subjected to ischemia by reducing coronary infusion to 15% of control flow for 30 minutes, then reestablishing normal flow, i.e., reperfusion, for an additional 20 minutes.
The vasodilator reponse then was remeasured by constriction and administration of vasodilating agent as described above.
The results of these experiments are shown in FIG. 2. Before the ischemic event, both Ach and NTG gave normal vasorelaxant results in all events. The hearts which received OP-1 24 hours prior to ischemia showed an approximately 70% response to ACh while the hearts which received OP-1 2 hours prior to ischemia showed a 55% response to ACh. The group which received vehicle alone showed a 40% response to ACh. Finally, the control group which was not subjected to ischemia showed an ACh response of approximately 95%. This shows that endothelium-dependent vasodilators exert a reduced vasodilator response following ischemia and reperfusion in the rat heart. Moreover, OP-1 significantly preserved endothelium-dependent dilation when provided 24 hours prior to induction of myocardial ischemia. No defect in vasodilation occurred in response to the direct vasodilator (NTG); NTG-induced vasodilation activities were 95% of initial in hearts subject to ischemia and 100% of initial nonischemic hearts.
Example 5
Effect of Morphogen on Neutrophil Adherence
The role of neutrophil adherence in endothelium dysfunction and the cardioprotective effects of morphogens in modulating this activity can be assessed using a standard polymorphonuclear neutrophil (PMN) adherence assay such as described in Lefer et al., (1992) J. Mol. Cell. Cardiol. 24: 385-393, disclosed hereinabove by reference. Briefly, segments of superior mesenteric artery were isolated from rats which had either been treated with morphogen (OP-1, 20 .mu.g) or 0.9% NaCl, 24 h prior to isolation of the artery. The segments were cleaned, cut into transverse rings of 1-2 mm in length, and these were subsequently cut open and incubated in K-H solution at 37.degree. C., pH 7.4. Neutrophils were prepared and fluorescently labelled using standard procedures (e.g., leukocytes were isolated from rats essentially following the procedure of Pertroft et. al. (1968) Exp Cell Res 50: 355-368, washed in phosphate buffered saline (PBS), purified by gradient centrifugation; and labelled by the method of Yuan et. al. (1990) Microvasc Res 40: 218-229.
Labelled neutrophils then were added to open ring baths and activated with 100 nM leukotriene B.sub.4 (LTB.sub.4). Rings were incubated for 20 minutes and the number of neutrophils adhering to the endothelial surface then determined visually by fluorescent microscopy.
As shown in FIG. 3, unstimulated PMNs (i.e., PMNs alone) added to the baths did not significantly adhere to the vascular endothelium. In rings taken from rats injected with 0.9% NaCl, activation of neutrophils with LTB.sub.4 (100 nM) greatly increased the number of PMNs adherent to the endothelium (P<0.001). OP-1 (20 .mu.g administered 24 h prior) significantly inhibited adherence of PMNs activated by LTB.sub.4 (P<0.01 from control).
Example 6
In Vivo Models for Ischemic-Reperfusion Protection in Lung, Nerve and Renal Tissue.
Other tissues seriously affected by ischemic-reperfusion injury include neural tissue, renal tissue and lung tissue. The effect of morphogens on alleviating the ischemic-reperfusion injury in these tissues may be assessed using methodologies and models known to those skilled in the art, and disclosed below. Similarly, a methodology also is provided for assessing the tissue-protective effects of a morphogen on damaged lung tissue following hyperoxia injury.
For example, the rabbit embolic stroke model provides a useful method for assessing the effect of morphogens on tissue injury following cerebral ischemia-reperfusion. The protocol disclosed below is essentially that of Phillips et al. (1989) Annals of Neurology 25:281-285, the disclosure of which is herein incorporated by reference. Briefly, white New England rabbits (2-3 kg) are anesthesized and placed on a respirator. The intracranial circulation then is selectively catheterized by the Seldinger technique. Baseline cerebral angiography then is performed, employing a digital substration unit. The distal internal carotid artery or its branches then is selectively embolized with 0.035 ml of 18-hour-aged autologous thrombus. Arterial occlusion is documented by repeat angiography immediately after embolization. After a time sufficient to induce cerebral infarcts (15 minutes or 90 minutes), reperfusion is induced by administering a bolus of a reperfusion agent such as the TPA analogue Fb-FB-CF (e.g., 0.8 mg/kg over 2 minutes).
The effect of morphogen on cerebral infarcts can be assessed by administering varying concentrations of morphogens, e.g., OP1, at different times preceding or following embolization and/or reperfusion. The rabbits are sacrificed 3-14 days post embolization and their brains prepared for neuropathological examination by fixing by immersion in 10% neutral buffered formalin for at least 2 weeks. The brains then are sectioned in a coronal plane at 2-3 mm intervals, numbered and submitted for standard histological processing in paraffin, and the degree of neutral tissue necrosis determined visually.
The renal-protective effects of morphogens on renal ischemia-reperfusion injury readily can be assessed using the mouse model disclosed by Oueliette, et al. (1990), J. Clin. Invest. 85:766-771, the disclosure of which is hereby incorporated by reference. Briefly, renal ischemia is induced surgically in 35-45 days old out-bred Swiss male mice by performing a standard right nephrectomy, and occluding the artery to the left kidney with a microaneurism clamp for 10-30 minutes. Morphogen then may be provided parentally at various times prior to or following, occlusion and/or reperfusion. The effects of morphogen then may be assessed by biological and histological evaluation using standard techniuques well known in the art.
The tissue protective effects of morphogen on tissue exposed to lethally high oxygen concentrations may be assessed by the following procedure. Adult rats (275-300 gms) first are provided with morphogen (e.g., hOP1) or vehicle only, and then are exposed to 96-98% oxygen essentially as described by Rinaldo et al (1983) Am. Rev. Respir. Dis. 130:1065, to induce hyperoxia. Animals are housed in plastic cages (38 cm.times.48 .times.m.times.21 cm). A cage containing 4-5 animals is placed in a 75 liter water-sealed plexiglass chamber. An atmosphere of 96-98% oxygen then is maintained by delivery of O.sub.2 gas (liquid O.sub.2). Gas flow through the chamber is adjusted to maintain at least 10 air changes/hr., temperature at 22.+-.1.degree. C., minimal levels of condensation within the cage, and carbon dioxide concentration of <0.5% as measured with a mass spetrophotometric medical as analyzer.
At the end of 72 hours all survivors are observed at room air for 1.5 hours and at longer time periods to assess degree of respiratory distress and cyanosis induced by the initial insult and subsequent immune insult and subsequent immune cell-mediated damage. The number of survivors at the end of the challenge is recorded and the treated groups compared with the untreated control group by chi-square test of proportions. Several of the surviving animals for each group are randomly chosen for histological processing of lung tissue.
Lung tissue for histological processing is fixed by infusion of 10% buffered formalin through a tracheal cannula at a constant pressure of 20 cm H.sub.2 O. After fixation for 24-48 hours, sections from each lobe are cut and subsequently stained with hematoxylin and eosin. Coded slides then are examined, preferably in a double-blind fashion for evidence of pathological changes such as edema, interstitial cellularity, and inflammatory response.
Example 7
Morphogen Inhibition of Cellular and Humoral Inflammatory Response
Morphogens described herein inhibit multinucleation of mononuclear phagocytic cells under conditions where these cells normally would be activated, e.g., in response to a tissue injury or the presence of a foreign substance. For example, in the absence of morphogen, an implanted substrate material (e.g., implanted subcutaneously) composed of, for example, mineralized bone, a ceramic such as titanium oxide or any other substrate that provokes multinucleated giant cell formation, rapidly becomes surrounded by multinucleated giant cells, e.g., activated phagocytes stimulated to respond and destroy the foreign object. In the presence of morphogen however, the recruited cells remain in their mononuclear precursor form and the matrix material is undisturbed. FIG. 4 illustrates this effect of morphogens, in a schematic representation of histology results of a titanium oxide substrate implanted subcutaneously. In the figure, "mg" means mononuclear giant cells and "ob" means osteoblasts. The substrate represented in FIG. 4B was implanted together with morphogen (OP-1) and newly formed osteoblasts are evident surrounding the substrate. By contrast, the substrate represented in FIG. 4A was implanted without morphogen and extensive multinucleated giant cell formation is evident surrounding the substrate. Accordingly, the morphogens' effect in inhibiting excessive bone mass loss in a mammal also may include inhibiting activation of these cells.
In addition, the morphogens described herein also suppress antibody production stimulated in response to a foreign antigen in a mammal. Specifically, when bovine bone collagen matrix alone was implanted in a bony site in a rat, a standard antibody response to the collag,n is stimulated in the rat as determined by standard anti-bovine collagen ELISA experiments performed on blood samples taken at four week intervals following implantation (e.g., between 12 and 20 weeks.) Serum anti-collagen antibody titers, measured by ELISA essentially following the procedure described by Nagler-Anderson et al, (1986) PNAS 83:7443-7446, the disclosure of which is incorporated herein by reference, increased consistently throughout the experiment. However, when the matrix was implanted together with a morphogen (e.g., OP-1, dispersed in the matrix and adsorbed thereto, essentially as described in U.S. Pat. No. 4,968,590) anti-bovine collagen antibody production was suppressed significantly. This ability of morphogen to suppress the humoral response is further evidence of morphogen utility in alleviating tissue damage associated with autoimmune diseases, including autoantibody diseases, such as rheumatoid arthritis.
Example 8
Morphogen protection of Gastrointestinal Tract Mucosa from Ulceration and Inflammation
Oral mucositis is a gastrointestinal tract inflammatory disease which involves ulcerations of the mouth mucosa as a consequence of, e.g., radiation therapy or chemotherapy. While not typically a chronic disease, the tissue destructive effects of oral mucositis mirror those of chronic inflammatory diseases such as IBD. The example below demonstrates morphogen efficacy in protecting the oral mucosa from oral mucositis in a hamster model, including both inhibiting inflammatory ulceration and enhancing regeneration of ulcerated tissue, retails of the protocol can be found in Sonis, et al., (1990) Oral Surg. Oral Med. Oral Pathol 69: 437-443, the disclosure of which is incorporated herein by reference. Based on these data, the morphogens described herein should be efficacious in treating chronic inflammatory diseases including IBD, arthritis, psoriasis and psoriatic arthritis, multiple sclerosis, and the like.
Golden syrian hamsters (6-8 wks old, Charles River Laboratories, Wilmington, Mass.) were divided into 3 test groups: Group 1, a placebo (e.g., saline) control, and a morphogen low dose group (100 ng) and a morphogen high dose group (1 .mu.g), Groups 2 and 3, respectively. Morphogen dosages were provided in 30% ethanol. Each group contained 12 animals.
Beginning on day 0 and continuing through day 5, Groups 2 and 3 received twice daily morphogen applications. On day 3, all groups began the mucositis-induction procedure. 5-fluorouracil (60 mg/kg) was injected intraperitoneally on days 3 and 5. On day 7, the right buccal pouch mucosa was superficially irritated with a calibrated 18 gauge needle. In untreated animals, severe ulcerative mucositis was induced in at least 80% of the animals by day 10.
For each administration of the vehicle control (placebo) or morphogen, administration was performed by first gently drying the cheek pouch mucosa, then providing an even application over the mucosal surface of the vehicle or morphogen material. A hydroxypropylcellulose-based coating was used to maintain contact of the morphogen with the mucosa. This coating provided at least 4 hours of contact time.
On day 12, two animals in each group were sacrificed for histological studies. The right buccal pouch mucosa and underlying connective tissue were dissected and fixed in 10% formalin using standard dissection and histology procedures. The specimens were mounted in paraffin and prepared for histologic examination. Sections then were stained with hematoxylin and eosin and were examined blindly by three oral pathologists with expertise in hamster histology and scored blind against a standard mucositis panel. The extent of atrophy, cellular infiltration, connective tissue breakdown, degree of ulceration and epithelialization were assessed.
The mean mucositis score for each group was determined daily for each experimental group for a period of 21 days by photography and visual examination of the right buccal cheek pouch. Differences between groups were determined using a standard `t` test, e.g., the Students' `t` test. In addition, data was evaluated between groups by comparing the numbers of animals with severe mucositis using Chi Square statistical analysis. The significance of differences in mean daily weights also was determined.
The experimental results are presented in FIG. 5, which graphs the effect of morphogen (high dose, squares; low dose, diamonds) and placebo (circles) on mean mucositis scores. Both low and high morphogen doses inhibit lesion formation significantly in a dose-dependent manner. In addition, histology results consistently showed significantly reduced amounts of tissue atrophy, cellular debris, and immune effector cells, including macrophages and activated neutrophils, in the morphogen-treated animals, as compared with the untreated, control animals.
Example 9
Morphogen Effect on Fibrogenesis and Scar Tissue Formation
The morphogens described herein induce tissue morphogenesis of damaged or lost tissue. The ability of these proteins to regenerate new tissue enhances the anti-inflammatory effect of these proteins. Provided below are a series of in vitro experiments demonstrating the ability of morphogens to induce migration and accumulation of mesenchymal cells. In addition, the experiments demonstrate that morphogens, unlike TGF-.beta., do not stimulate fibrogenesis or scar tissue formation. Specifically, morphogens do not stimulate production of collagen, hyaluronic acid (HA) or metalloproteinases in primary fibroblasts, all of which are required for fibrogenesis or scar tissue formation. By contrast, TGF-.beta., a known inducer of fibrosis, but not of tissue morphogenesis, does stimulate production of these fibrosis markers.
Chemotaxis and migration of mesenchymal progenitor cells were measured in modified Boyden chambers essentially as described by Fava, R. A. et al (1991) J. Exp. Med. 173: 1121-1132, the disclosure of which is incorporated herein by reference, using polycarbonate filters of 2, 3 and 8 micron ports to measure migration of progenitor neutrophils, monocytes and fibroblasts. Chemotaxis was measured over a range of morphogen concentrations, e.g., 10.sup.-1 M to 10.sup.-12 M OP-1. For progenitor neutrophils and monocytes, 10.sup.-18 -10.sup.-17 M OP-1 consistently induced maximal migration, and 10.sup.-14 to 10.sup.-13 M OP-1 maximally induced migration of progenitor fibroblasts. In all cases the chemotactic activity could be inhibited with anti-OP-1 antibody. Similar migration activities also were measured and observed with TGF-.beta..
The effect of morphogen on fibrogenesis was determined by evaluating fibroblast production of hyaluronic acid (HA), collagen, collagenese and tissue inhibitor of metalloproteinases (TIMP).
Human fibroblasts were established from explants of infant foreskins and maintained in monolayer culture using standard culturing procedures. (See, for example, (1976) J. Exp. Med. 144: 1188-1203.) Briefly, fibroblasts were grown in maintenance medium consisting of Eagle's MEM, supplemented with nonessential amino acids, ascorbic acid (50 .mu.g/ml), NaHCO.sub.3 and HEPES buffers (pH 7.2), penicillin (100 U/ml), streptomycin (100 .mu.g/ml), amphotericin B (1 .mu.g/ml) and 9% heat inactivated FCS. Fibroblasts used as target cells to measure chemotaxis were maintained in 150 mm diameter glass petri dishes. Fibroblasts used in assays to measure synthesis of collagen, hyaluronic acid, collagenase and tissue inhibitors of metalloproteinases (TIMP) were grown in 100 mm diameter plastic tissue culture petri dishes.
The effects of morphogen on fibroblast production of hyaluronic acid, collagens, collagenase and TIMP were determined by standard assays (See, for example, Posttethwaite et dl. (.1989) J. Clin. Invest. 83: 629-636, Posttethwaithe (1988) J./ Cell Biol. 106: 311-318 and Clark et al (1985) Arch. Bio-chem Biophys. 241: 36-44, the disclosures of which are incorporated by reference.) For these assays, fibroblasts were transferred to 24-well tissue culture plates at a density of 8.times.10.sup.4 cells per well. Fibroblasts were grown confluency in maintenance medium containing 9% FCS for 72 h and then grown in serum-free maintenance medium for 24 h. Medium was then removed from each well and various concentrations of OP-1 (recombinantly produced mature or soluble form) or TGF-.beta.-1 (R&D Systems, Minneapolis) in 50 .mu.l PBS were added to triplicate wells containing the confluent fibroblast monolayers. For experiments that measured production of collagenase and TIMP, maintenance medium (450 .mu.l) containing 5% FCS was added to each well, and culture supernatants were harvested from each well 48 h later and stored at -70.degree. C. until assayed. For experiments that assessed HA production, maintenance medium (450 .mu.l) containing 2.5% FCS was added to each well, and cultures grown for 48 h. For experiments that measured fibroblast production of collagens, serum-free maintenance medium (450 .mu.l) without non-essential amino acids was added to each well and cultures grown for 72 h. Fibroblast production of HA was measured by labeling newly synthesized glycosaminoglycans (GAG) with [.sup.3 H]-acetate the last 24 h of culture and quantitating released radioactivity after incubation with hyaluronidase from Streptomyces hyalurolyticus (ICN Biochemicals, Cleveland, Ohio) which specifically degrades hyaluronic acid. Production of total collagen by fibroblasts was measured using a collagenase-sensitive protein assay that reflects [.sup.3 H]-proline incorporation the last 24 h of culture into newly synthesized collagens. Collagenase and TIMP protein levels in fibroblast cultures supernatants was measured by specific ELISAs.
As shown in FIG. 6, OP1 does not stimulate significant collagen or HA production, as compared with TGF-.beta.. In the figure, panel A shows OP-1 efect on collagen production, panel B shows TGF-.beta. effect on collagen production, and panels C and D show OP-1 (panel C) and TGF-.beta. (panel D) effect on HA production. The morphogen results were the same whether the soluble or mature form of OP1 was used. By contrast, the latent form of TGF-.beta. (e.g., pro domain-associated form of TGF-.beta.) was not active.
Example 10
Morphogen Inhibition of Epithelial Cell Proliferation
This example demonstrates the ability of morphogens to inhibit epithelial cell proliferation in vitro, as determined by .sup.3 H-thymidine uptake using culture cells from a mink lung epithelial cell line (ATCC No. CCL 64), and standard mammalian cell culturing procedures. Briefly, cells were grown to confluency in Eagle's minimum essential medium (EMEM) supplemented with 10% fetal bovine serum (FBS), 200 units/ml penicillin, and 200 .mu.g/ml streptomycin, and used to seed a 48-well cell culture plate at a cell density of 200,000 cells per well. When this culture became confluent, the media was replaced with 0.5 ml of EMEM containing 1% FBS and penicillin/streptomycin and the culture incubated for 24 hours at 37 C. Morphogen test samples in EMEM containing 5% FBS then were added to the wells, and the cells incubated for another 18 hours. After incubation, 1.0 .mu.Ci of .sup.3 H-thymidine in 10 .mu.l was added to each well, and the cells incubated for four hours at 37 C. The media then was removed and the cells washed once with ice-cold phosphate-buffer saline and DNA precipitated by adding 0.5 ml of 10% TCA to each well and incubating at room temperature of 15 minutes. The cells then were washed three times with ice-cold distilled water, lysed with 0.5 ml 0.4 M NaOH, and the lysate from each well then transferred to a scintillation vial and the radioactivity recorded using a scintillation counter (Smith-Kline Beckman).
The results are presented in Table III, below. The anti-proliferative effect of the various morphogens tested was expressed as the counts of 3H-thymidine (.times.1000) integrated into DNA, and were compared with untreated cells (negative control) and TGF-.beta. (1 ng), a local-acting factor also known to inhibit epithelial cell proliferation. COP-5 and COP-7 are biosynthetic constructs that previously have been shown to have osteogenic activity, capable of inducing the complete cascade resulting in endochondral bone formation in a standard rat bone assay (see U.S. Pat. No. 5,011,691.) The morphogens significantly inhibit epithelial cell proliferation. Similar experiments, performed with the morphogens COP-16, bOP (bone-purified osteogenic protein, a dimeric protein comprising CBMP2 and OP-1), and recombinant OP-1, also inhibit cell proliferation. bOP and COP-16 also induce endochondral bone formation (see U.S. Pat. Nos. 4,968,590 and 5,011,691.)
TABLE III______________________________________ Thymidine uptake (.times.1000)______________________________________control 50.048, 53.692COP-7-1 (10 ng) 11.874COP-7-2 (3 ng) 11.136COP-5-1 (66 ng) 16.094COP-5-2 (164 ng) 14.43TGF-.beta. (1 ng) 1.86, 1.478______________________________________
Example 11
Morphogen Treatment of a Systemic Inflammatory Disease
The following example provides a rat adjuvant-induced arthritis model for demonstrating morphogen efficacy in treating arthritis and other systemic inflammatory diseases. Rat adjuvant-induced arthritis induces a systemic inflammatory disease with bone and cartilage changes similar to those observed in rhematoid arthritis, but in an accelerated time span (see, for example, Pearson (1964) Arth. Rheum. 7:80). A detailed description of the protocol is provided in Walz, et al., (1971) J. Pharmac. Exp. Ther. 178: 223-231, the disclosure of which is incorporated herein by reference.
Briefly, Sprague-Dawley female rats (e.g., Charles River Laboratories, Wilmington, Mass.) are randomized into 3 groups: control; morphogen, low dose (e.g., 1-10 .mu.g/kg weight per day) and morphogen, high dose (e.g., 10-20 .mu.g/kg weight per day), referred to as Groups 1, 2, and 3, respectively.
Adjuvant arthritis is induced in all three groups by injection of 0.05 ml of a suspension of 1.5% dead Mycobacterium butyricum in mineral oil into the subplantar surface of the right hand paw. On Day 18 after adjavant injection, the limb volumes of both hind limbs are determined. In the absence of morphogen treatment, a systemic arthritic condition is induced in the rats by this time, as determined by rats with significant swelling of the uninjected hind limbs (<2.3 ml, volume measured by mercury displacement). Subsequent determinations of paw edema and x-ray scores are made on the uninjected hind limb. Rats in Group 2and 3 also are dosed orally daily, beginning on Day 1, with morphogen. Limb volumes are recorded on Days 29 and 50 after adjuvant injection and edema determined by volume difference compared to Day 18. The uninjected hind limb on each rat was x-rayed on Day 50 and the joint damage assayed on an arbitrary scale of 1 to 10 (1=no damage, 10=maximum damage). Data on differences between control and treated groups (Day 29 edema, Day 50 edema and Day 50 x-ray scores) are analyzed by using a standard "t-test". Morphogen-treated rats show consistently reduced joint damage (e.g., decreased in edema and in x-ray scores) as compared with untreated control rats.
As another, alternative example, Groups 2 and 3 are dosed daily with morphogen beginning on Day 18 and continuing through Day 50 to demonstrate the efficacy of morphogens in arthritic animals.
Example 12
Morphogen Inhibition of Localized Edema
The following example demonstrates morphogen efficacy in inhibiting a localized inflammatory response in a standard rat edema model. Experimental rats (e.g., Long-Evans from Charles River Laboratories, Wilmington, Mass.) are divided into three groups: Group 1, a negative control, which receives vehicle alone; Group 2, a positive control, to which is administered a well-known characterized anti-inflammatory agent (e.g., indomethacin), and Group 3, to which morphogen is provided.
Groups 2 and 3 may be further subdivided to test low, medium and high doses (e.g., Group 2: 1.0 mg/kg, 3.0 mg/kg and 9.0 mg/kg indomethacin; Group 3: 0.1-5 .mu.g; 5-20 .mu.g, and 20-50 .mu.g of morphogen). Sixty minutes after indomethacin or morphogen is provided to the rats of Group 2 or 3 (e.g., as by injection into the tail vein, or by oral gavage) inflammation is induced in all rats by a sub-plantar injection of a 1% carrageenin solution (50 .mu.l) into the right hind paw. Three hours after carrageenin administration paw thickness is measured as an indication of edema (e.g., swelling) and induced inflammatory response to the injected carrageenin solution.
Significant swelling is evident in untreated rats by three hours after carrageenin injection. Inflammation also is measured by histology by standard means, following euthanasia e.g.: the right hind paw from each animal is removed at the ankle joint and weighed and foot pad tissue is fixed in 10% neutral buffered formalin, and slides prepared for visual examination by staining the prepared tissue with hematoxylin and eosin.
The morphogen-treated rats show substantially reduced edema induction following carrageenin injection as compared with the untreated rats.
Example 13
Morphogen Treatment of Allergic Encephalomyelitis
The following example demonstrates morphogen efficacy in treating experimental allergic encephalomyelitis (EAE) in a rat. EAE is a well-characterized animal model for multiple sclerosis, an autoimmune disease. A detailed description of the protocol is disclosed in Kuruvilla, et al., (1991) PNAS 88:2918-2921, the disclosure of which is incorporated herein by reference.
Briefly, EAE is induced in rats (e.g., Long-Evans, Charles River Laboratories, Wilmington, Mass.) by injection of a CNS tissue (e.g., spinal cord) homogenate in complete Freund's adjuvant (CFA) on days -44, -30 and 0 (last day of immunization), by subcutaneous injection to three sites on the animal's back. Morphogen is administered daily by interperitoneal injection beginning on day -31. Preferably, a series of morphogen dose ranges is evaluated (e.g., low, medium and high) as for Example 12, above.) Control rats receive morphogen vehicle only (e.g. 0.9% NaCl or buffered saline). Rats are examined daily for signs of disease and graded on an increasing severity scale of 0-4.
In the absence of morphogen treatment, significant neurological dysfunction (e.g., hind and fore limb weakness, progressing to total hind limb paralysis) is evident by day +7 to +10. Hematology, serum chemistry profiles and histology are performed to evaluate the degree of tissue necropsy using standard procedures. Morphogen treatment significantly inhibits the neurological dysfunction normally evident in an EAE animal. In addition, the histopathological markers typically associated with EAE are absent in the morphogen-treated animals.
Example 14
Morphogen Treatment of Collagen-Induced Arthritis
The following example demonstrates the efficacy of morphogens in inhibiting the inflammatory response in a collagen-induced arthritis (CIA) in a rat. CIA is a well-characterized animal model for rheumatoid arthritis, an autoimmune disease. The protocol disclosed is essentially that disclosed in Kuruvilla et al., (1991) PNAS 88:2918-2921, incorporated by reference hereinabove. Briefly, CIA is induced in experimental rats (e.g., Long-Evans, Charles River Laboratories, Wilmington), by multiple intradermal injection of bovine Type II collagen (e.g., 100 .mu.g) in CFA (0.2 ml) on Day 1. Animals are divided into two groups: Group 1, control animals, which receive vehicle alone, and Group 2: morphogen-treated animals, which, preferably, are subdivided into low, medium and high dose ranges, as described for Example 13, above. Morphogen is administered daily (e.g., by tail vein injection) beginning at different times following collagen injection, e.g., beginning on day 7, 14, 28, 35 and 42. Animals are evaluated visually and paw thickness and body weight is monitored throughout the experiment. Animals are sacrificed on day 60 and the proximal and distal limb joints, and ear, tail and spinal cord prepared for histological evaluation as described for Examples 12 and 13, above. In a variation of the experiment, morphogen may be administered for prescribed periods, e.g., five day periods, beginning at different times following collagen injection (e.g., on days 0-4, 7-11, 14-18, 28-32.)
In the absence of morphogen treatment, an arthritic condition typically is induced by 30 days post collagen injection. In morphogen-treated animals, CIA is suppressed and the histopathological changes typically evidenced in control CIA-induced animals are absent: e.g., accumulations of activated mononuclear inflammatory cells and fibrous connective tissue. In addition, consistent with the results in Example 7, above, serum anti-collagen antibody titers are suppressed significantly in the morphogen-treated animals.
Example 15
Screening Assay for Candidate Compounds which Alter Endogenous Morphogen Levels
Candidate compound(s) which may be administered to affect the level of a given morphogen may be found using the following screening assay, in which the level of morphogen production by a cell type which produces measurable levels of the morphogen is determined with and without incubating the cell in culture with the compound, in order to assess the effects of the compound on the cell. This can be accomplished by detection of the morphogen either at the protein or RNA level. A more detailed description also may be found in U.S. Ser. No. 752,861, incorporated hereinabove by reference.
15.1 Growth of Cells in Culture
Cell cultures of kidney, adrenals, urinary bladder, brain, or other organs, may be prepared as described widely in the literature. For example, kidneys may be explanted from neonatal or new born or young or adult rodents (mouse or rat) and used in organ culture as whole or sliced (1-4 mm) tissues. Primary tissue cultures and established cell lines, also derived from kidney, adrenals, urinary, bladders brain, mammary, or other tissues may be established in multiwell plates (6 well or 24 well) according to conventional cell culture techniques, and are cultured in the absence or presence of serum for a period of time (1-7 days). Cells may be cultured, for example, in Dulbecco's Modified Eagle medium (Gibco, Long Island, N.Y.) containing serum (e.g., fetal calf serum at 1%-10%, Gibco) or in serum-deprived medium, as desired, or in defined medium (e.g., containing insulin, transferrin, glucose, albumin, or other growth factors).
Samples for testing the level of morphogen production includes culture supernatants or cell lysates, collected periodically and evaluated for OP-1 production by immunoblot analysis (Sambrook et al., eds., 1989, Molecular Cloning, Cold Spring Harbor Press, Cold Spring Harbor, N.Y.), or a portion of the cell culture itself, collected periodically and used to prepare polyA+ RNA for RNA analysis. To monitor de novo OP-1 synthesis, some cultures are labeled according to conventional procedures with an .sup.35 S-methionine/.sup.35 S-cysteine mixture for 6-24 hours and then evaluated to OP-1 synthesis by conventional immunoprecipitation methods.
15.2 Determination of Level of Morphogenic Protein
In order to quantitate the production of a morphogenic protein by a cell type, an immunoassay may be performed to detect the morphogen using a polyclonal or monoclonal antibody specific for that protein. For example, OP-1 may be detected using a polyclonal antibody specific for OP-1 in an ELISA, as follows.
1 .mu.g/100 .mu.l of affinity-purified polyclonal rabbit IgG specific for OP-1 is added to each well of a 96-well plate and incubated at 37.degree. C. for an hour. The wells are washed four times with 0.167M sodium borate buffer with 0.15 M NaCl (BSB), pH 8.2, containing 0.1% Tween 20. To minimize non-specific binding, the wells are blocked by filling completely with 1% bovine serum albumin (BSA) in BSB and incubating for 1 hour at 37.degree. C. The wells are then washed four times with BSB containing 0.1% Tween 20. A 100 .mu.l aliquot of an appropriate dilution of each of the test samples of cell culture supernatant is added to each well in triplicate and incubated at 37.degree. C. for 30 min. After incubation, 100 .mu.l biotinylated rabbit anti-OP-i serum (stock solution is about 1 mg/ml and diluted 1:400 in BSB containing 1% BSA before use) is added to each well and incubated at 37.degree. C. for 30 min. The wells are then washed four times with BSB containing 0.1% Tween 20. 100 .mu.l strepavidin-alkaline (Southern Biotechnology Associates, Inc. Birmingham, Ala., diluted 1:2000 in BSB containing 0.1% Tween 20 before use) is added to each well and incubated at 37.degree. C. for 30 min. The plates are washed four times with 0.5M Tris buffered Saline (TBS), pH 7.2. 50 .mu.l substrate (ELISA Amplification System Kit, Life Technologies, Inc., Bethesda, Md.) is added to each well incubated at room temperature for 15 min. Then, 50 .mu.l amplifier (from the same amplification system kit) is added and incubated for another 15 min at room temperature. The reaction is stopped by the addition of 50 .mu.l 0.3 M sulphuric acid. The OD at 490 nm of the solution in each well is recorded. To quantitate OP-1 in culture media, a OP-1 standard curve is performed in parallel with the test samples.
Polyclonal antibody may be prepared as follows. Each rabbit is given a primary immunization of 100 .mu.g/500 .mu.l E. coli produced OP-1 monomer (amino acids 328-431 in SEQ ID NO:5) in 0.1% SDS mixed with 500 .mu.l Complete Freund's Adjuvant. The antigen is injected subcutaneously at multiple sites on the back and flanks of the animal. The rabbit is boosted after a month in the same manner using incomplete Freund's Adjuvant. Test bleeds are taken from the ear vein seven days later. Two additional boosts and test bleeds are performed at monthly intervals until antibody against OP-1 is detected in the serum using an ELISA assay. Then, the rabbit is boosted monthly with 100 .mu.g of antigen and bled (15 ml per bleed) at days seven and ten after boosting.
Monoclonal antibody specific for a given morphogen may be prepared as follows. A mouse is given two injections of E. coli produced OP-1 monomer. The first injection contains 100 .mu.g of OP-1 in complete Freund's adjuvant and is given subcutaneously. The second injection contains 50 .mu.g of OP-1 in incomplete adjuvant and is given intraperitoneally. The mouse then receives a total of 230 .mu.g of OP-1 (amino acids 307-431 in SEQ ID NO:5) in four intraperitoneal injections at various times over an eight month period. One week prior to fusion, both mice are boosted intraperitoneally with 100 pg of OP-1 (307-431) and 30 .mu.g of the N-terminal peptide (Ser.sub.293 -Asn.sub.309 -Cys) conjugated through the added cysteine to bovine serum albumin with SMCC crosslinking agent. This boost was repeated five days (IP), four days (IP), three days (IP) and one day (IV) prior to fusion. The mouse spleen cells are then fused to myeloma (e.g., 653) cells at a ratio of 1:1 using PEG 1500 (Boeringer Mannheim), and the cell fusion is plated and screened for OP-1-specific antibodies using OP-1 (307-431) as antigen. The cell fusion and monoclonal screening then are according to standard procedures well described in standard texts widely available in the art.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
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#u Tyr Val Ser Phe Arg# 45- Asp Leu Gly Trp Gln Asp Trp Ile Ile Ala Pr - #o Glu Gly Tyr Ala Ala# 60- Tyr Tyr Cys Glu Gly Glu Cys Ala Phe Pro Le - #u Asn Ser Tyr Met Asn# 80- Ala Thr Asn His Ala Ile Val Gln Thr Leu Va - #l His Phe Ile Asn Pro# 95- Asp Thr Val Pro Lys Pro Cys Cys Ala Pro Th - #r Gln Leu Asn Ala Ile# 110- Ser Val Leu Tyr Phe Asp Asp Ser Ser Asn Va - #l Ile Leu Lys Lys Tyr# 125- Arg Asn Met Val Val Arg Ala Cys Gly Cys Hi - #s# 135- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 139 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: HOMO SAPI - #ENS (F) TISSUE TYPE: HIPPOC - #AMPUS- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..139#/label= HOP2-MATUREINFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:- Ala Val Arg Pro Leu Arg Arg Arg Gln Pro Ly - #s Lys Ser Asn Glu Leu# 15- Pro Gln Ala Asn Arg Leu Pro Gly Ile Phe As - #p Asp Val His Gly Ser# 30- His Gly Arg Gln Val Cys Arg Arg His Glu Le - #u Tyr Val Ser Phe Gln# 45- Asp Leu Gly Trp Leu Asp Trp Val Ile Ala Pr - #o Gln Gly Tyr Ser Ala# 60- Tyr Tyr Cys Glu Gly Glu Cys Ser Phe Pro Le - #u Asp Ser Cys Met Asn# 80- Ala Thr Asn His Ala Ile Leu Gln Ser Leu Va - #l His Leu Met Lys Pro# 95- Asn Ala Val Pro Lys Ala Cys Cys Ala Pro Th - #r Lys Leu Ser Ala Thr# 110- Ser Val Leu Tyr Tyr Asp Ser Ser Asn Asn Va - #l Ile Leu Arg Lys His# 125- Arg Asn Met Val Val Lys Ala Cys Gly Cys Hi - #s# 135- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 139 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: MURIDAE (F) TISSUE TYPE: EMBRYO- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..139#/label= MOP2-MATUREINFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:- Ala Ala Arg Pro Leu Lys Arg Arg Gln Pro Ly - #s Lys Thr Asn Glu Leu# 15- Pro His Pro Asn Lys Leu Pro Gly Ile Phe As - #p Asp Gly His Gly Ser# 30- Arg Gly Arg Glu Val Cys Arg Arg His Glu Le - #u Tyr Val Ser Phe Arg# 45- Asp Leu Gly Trp Leu Asp Trp Val Ile Ala Pr - #o Gln Gly Tyr Ser Ala# 60- Tyr Tyr Cys Glu Gly Glu Cys Ala Phe Pro Le - #u Asp Ser Cys Met Asn# 80- Ala Thr Asn His Ala Ile Leu Gln Ser Leu Va - #l His Leu Met Lys Pro# 95- Asp Val Val Pro Lys Ala Cys Cys Ala Pro Th - #r Lys Leu Ser Ala Thr# 110- Ser Val Leu Tyr Tyr Asp Ser Ser Asn Asn Va - #l Ile Leu Arg Lys His# 125- Arg Asn Met Val Val Lys Ala Cys Gly Cys Hi - #s# 135- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 101 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: bovinae- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..101#/label= CBMP-2A-FX INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:- Cys Lys Arg His Pro Leu Tyr Val Asp Phe Se - #r Asp Val Gly Trp Asn# 15- Asp Trp Ile Val Ala Pro Pro Gly Tyr His Al - #a Phe Tyr Cys His Gly# 30- Glu Cys Pro Phe Pro Leu Ala Asp His Leu As - #n Ser Thr Asn His Ala# 45- Ile Val Gln Thr Leu Val Asn Ser Val Asn Se - #r Lys Ile Pro Lys Ala# 60- Cys Cys Val Pro Thr Glu Leu Ser Ala Ile Se - #r Met Leu Tyr Leu Asp# 80- Glu Asn Glu Lys Val Val Leu Lys Asn Tyr Gl - #n Asp Met Val Val Glu# 95- Gly Cys Gly Cys Arg 100- (2) INFORMATION FOR SEQ ID NO:10:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 101 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: HOMO SAPI - #ENS (F) TISSUE TYPE: hippoc - #ampus- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..101#/label= CBMP-2B-FX INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:- Cys Arg Arg His Ser Leu Tyr Val Asp Phe Se - #r Asp Val Gly Trp Asn# 15- Asp Trp Ile Val Ala Pro Pro Gly Tyr Gln Al - #a Phe Tyr Cys His Gly# 30- Asp Cys Pro Phe Pro Leu Ala Asp His Leu As - #n Ser Thr Asn His Ala# 45- Ile Val Gln Thr Leu Val Asn Ser Val Asn Se - #r Ser Ile Pro Lys Ala# 60- Cys Cys Val Pro Thr Glu Leu Ser Ala Ile Se - #r Met Leu Tyr Leu Asp# 80- Glu Tyr Asp Lys Val Val Leu Lys Asn Tyr Gl - #n Glu Met Val Val Glu# 95- Gly Cys Gly Cys Arg 100- (2) INFORMATION FOR SEQ ID NO:11:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE:#MELANOGASTER ORGANISM: DROSOPHILA- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..101#/label= DPP-FXTHER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:- Cys Arg Arg His Ser Leu Tyr Val Asp Phe Se - #r Asp Val Gly Trp Asp# 15- Asp Trp Ile Val Ala Pro Leu Gly Tyr Asp Al - #a Tyr Tyr Cys His Gly# 30- Lys Cys Pro Phe Pro Leu Ala Asp His Phe As - #n Ser Thr Asn His Ala# 45- Val Val Gln Thr Leu Val Asn Asn Asn Asn Pr - #o Gly Lys Val Pro Lys# 60- Ala Cys Cys Val Pro Thr Gln Leu Asp Ser Va - #l Ala Met Leu Tyr Leu# 80- Asn Asp Gln Ser Thr Val Val Leu Lys Asn Ty - #r Gln Glu Met Thr Val# 95- Val Gly Cys Gly Cys Arg 100- (2) INFORMATION FOR SEQ ID NO:12:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: XENOPUS- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..102#/label= VGL-FXTHER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:- Cys Lys Lys Arg His Leu Tyr Val Glu Phe Ly - #s Asp Val Gly Trp Gln# 15- Asn Trp Val Ile Ala Pro Gln Gly Tyr Met Al - #a Asn Tyr Cys Tyr Gly# 30- Glu Cys Pro Tyr Pro Leu Thr Glu Ile Leu As - #n Gly Ser Asn His Ala# 45- Ile Leu Gln Thr Leu Val His Ser Ile Glu Pr - #o Glu Asp Ile Pro Leu# 60- Pro Cys Cys Val Pro Thr Lys Met Ser Pro Il - #e Ser Met Leu Phe Tyr# 80- Asp Asn Asn Asp Asn Val Val Leu Arg His Ty - #r Glu Asn Met Ala Val# 95- Asp Glu Cys Gly Cys Arg 100- (2) INFORMATION FOR SEQ ID NO:13:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: MURIDAE- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..102#/label= VGR-1-FXER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:- Cys Lys Lys His Glu Leu Tyr Val Ser Phe Gl - #n Asp Val Gly Trp Gln# 15- Asp Trp Ile Ile Ala Pro Lys Gly Tyr Ala Al - #a Asn Tyr Cys Asp Gly# 30- Glu Cys Ser Phe Pro Leu Asn Ala His Met As - #n Ala Thr Asn His Ala# 45- Ile Val Gln Thr Leu Val His Val Met Asn Pr - #o Glu Tyr Val Pro Lys# 60- Pro Cys Cys Ala Pro Thr Lys Val Asn Ala Il - #e Ser Val Leu Tyr Phe# 80- Asp Asp Asn Ser Asn Val Ile Leu Lys Lys Ty - #r Arg Asn Met Val Val# 95- Arg Ala Cys Gly Cys His 100- (2) INFORMATION FOR SEQ ID NO:14:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 106 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (iii) HYPOTHETICAL: NO- (iv) ANTI-SENSE: NO- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens (F) TISSUE TYPE: brain- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..106#/note= "GDF-1 (fx)"INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:- Cys Arg Ala Arg Arg Leu Tyr Val Ser Phe Ar - #g Glu Val Gly Trp His# 15- Arg Trp Val Ile Ala Pro Arg Gly Phe Leu Al - #a Asn Tyr Cys Gln Gly# 30- Gln Cys Ala Leu Pro Val Ala Leu Ser Gly Se - #r Gly Gly Pro Pro Ala# 45- Leu Asn His Ala Val Leu Arg Ala Leu Met Hi - #s Ala Ala Ala Pro Gly# 60- Ala Ala Asp Leu Pro Cys Cys Val Pro Ala Ar - #g Leu Ser Pro Ile Ser# 80- Val Leu Phe Phe Asp Asn Ser Asp Asn Val Va - #l Leu Arg Gln Tyr Glu# 95- Asp Met Val Val Asp Glu Cys Gly Cys Arg# 105- (2) INFORMATION FOR SEQ ID NO:15:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 5 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:- Cys Xaa Xaa Xaa Xaa1 5- (2) INFORMATION FOR SEQ ID NO:16:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1822 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA- (iii) HYPOTHETICAL: NO- (iv) ANTI-SENSE: NO- (vi) ORIGINAL SOURCE: (A) ORGANISM: HOMO SAPI - #ENS (F) TISSUE TYPE: HIPPOC - #AMPUS- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 49..1341 (C) IDENTIFICATION METHOD: - # experimental#/function= "OSTEOGENIC PROTEIN" /product=- # "OP1" /evidence=- # EXPERIMENTAL /standard.sub.-- - #name= "OP1"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #16:#CAC GTG 57AGCCCGG AGCCCGGGTA GCGCGTAGAG CCGGCGCG ATG# Met - # His Val# 1- CGC TCA CTG CGA GCT GCG GCG CCG CAC AGC TT - #C GTG GCG CTC TGG GCA 105Arg Ser Leu Arg Ala Ala Ala Pro His Ser Ph - #e Val Ala Leu Trp Ala# 15- CCC CTG TTC CTG CTG CGC TCC GCC CTG GCC GA - #C TTC AGC CTG GAC AAC 153Pro Leu Phe Leu Leu Arg Ser Ala Leu Ala As - #p Phe Ser Leu Asp Asn# 35- GAG GTG CAC TCG AGC TTC ATC CAC CGG CGC CT - #C CGC AGC CAG GAG CGG 201Glu Val His Ser Ser Phe Ile His Arg Arg Le - #u Arg Ser Gln Glu Arg# 50- CGG GAG ATG CAG CGC GAG ATC CTC TCC ATT TT - #G GGC TTG CCC CAC CGC 249Arg Glu Met Gln Arg Glu Ile Leu Ser Ile Le - #u Gly Leu Pro His Arg# 65- CCG CGC CCG CAC CTC CAG GGC AAG CAC AAC TC - #G GCA CCC ATG TTC ATG 297Pro Arg Pro His Leu Gln Gly Lys His Asn Se - #r Ala Pro Met Phe Met# 80- CTG GAC CTG TAC AAC GCC ATG GCG GTG GAG GA - #G GGC GGC GGG CCC GGC 345Leu Asp Leu Tyr Asn Ala Met Ala Val Glu Gl - #u Gly Gly Gly Pro Gly# 95- GGC CAG GGC TTC TCC TAC CCC TAC AAG GCC GT - #C TTC AGT ACC CAG GGC 393Gly Gln Gly Phe Ser Tyr Pro Tyr Lys Ala Va - #l Phe Ser Thr Gln Gly100 1 - #05 1 - #10 1 -#15- CCC CCT CTG GCC AGC CTG CAA GAT AGC CAT TT - #C CTC ACC GAC GCC GAC 441Pro Pro Leu Ala Ser Leu Gln Asp Ser His Ph - #e Leu Thr Asp Ala Asp# 130- ATG GTC ATG AGC TTC GTC AAC CTC GTG GAA CA - #T GAC AAG GAA TTC TTC 489Met Val Met Ser Phe Val Asn Leu Val Glu Hi - #s Asp Lys Glu Phe Phe# 145- CAC CCA CGC TAC CAC CAT CGA GAG TTC CGG TT - #T GAT CTT TCC AAG ATC 537His Pro Arg Tyr His His Arg Glu Phe Arg Ph - #e Asp Leu Ser Lys Ile# 160- CCA GAA GGG GAA GCT GTC ACG GCA GCC GAA TT - #C CGG ATC TAC AAG GAC 585Pro Glu Gly Glu Ala Val Thr Ala Ala Glu Ph - #e Arg Ile Tyr Lys Asp# 175- TAC ATC CGG GAA CGC TTC GAC AAT GAG ACG TT - #C CGG ATC AGC GTT TAT 633Tyr Ile Arg Glu Arg Phe Asp Asn Glu Thr Ph - #e Arg Ile Ser Val Tyr180 1 - #85 1 - #90 1 -#95- CAG GTG CTC CAG GAG CAC TTG GGC AGG GAA TC - #G GAT CTC TTC CTG CTC 681Gln Val Leu Gln Glu His Leu Gly Arg Glu Se - #r Asp Leu Phe Leu Leu# 210- GAC AGC CGT ACC CTC TGG GCC TCG GAG GAG GG - #C TGG CTG GTG TTT GAC 729Asp Ser Arg Thr Leu Trp Ala Ser Glu Glu Gl - #y Trp Leu Val Phe Asp# 225- ATC ACA GCC ACC AGC AAC CAC TGG GTG GTC AA - #T CCG CGG CAC AAC CTG 777Ile Thr Ala Thr Ser Asn His Trp Val Val As - #n Pro Arg His Asn Leu# 240- GGC CTG CAG CTC TCG GTG GAG ACG CTG GAT GG - #G CAG AGC ATC AAC CCC 825Gly Leu Gln Leu Ser Val Glu Thr Leu Asp Gl - #y Gln Ser Ile Asn Pro# 255- AAG TTG GCG GGC CTG ATT GGG CGG CAC GGG CC - #C CAG AAC AAG CAG CCC 873Lys Leu Ala Gly Leu Ile Gly Arg His Gly Pr - #o Gln Asn Lys Gln Pro260 2 - #65 2 - #70 2 -#75- TTC ATG GTG GCT TTC TTC AAG GCC ACG GAG GT - #C CAC TTC CGC AGC ATC 921Phe Met Val Ala Phe Phe Lys Ala Thr Glu Va - #l His Phe Arg Ser Ile# 290- CGG TCC ACG GGG AGC AAA CAG CGC AGC CAG AA - #C CGC TCC AAG ACG CCC 969Arg Ser Thr Gly Ser Lys Gln Arg Ser Gln As - #n Arg Ser Lys Thr Pro# 305- AAG AAC CAG GAA GCC CTG CGG ATG GCC AAC GT - #G GCA GAG AAC AGC AGC1017Lys Asn Gln Glu Ala Leu Arg Met Ala Asn Va - #l Ala Glu Asn Ser Ser# 320- AGC GAC CAG AGG CAG GCC TGT AAG AAG CAC GA - #G CTG TAT GTC AGC TTC1065Ser Asp Gln Arg Gln Ala Cys Lys Lys His Gl - #u Leu Tyr Val Ser Phe# 335- CGA GAC CTG GGC TGG CAG GAC TGG ATC ATC GC - #G CCT GAA GGC TAC GCC1113Arg Asp Leu Gly Trp Gln Asp Trp Ile Ile Al - #a Pro Glu Gly Tyr Ala340 3 - #45 3 - #50 3 -#55- GCC TAC TAC TGT GAG GGG GAG TGT GCC TTC CC - #T CTG AAC TCC TAC ATG1161Ala Tyr Tyr Cys Glu Gly Glu Cys Ala Phe Pr - #o Leu Asn Ser Tyr Met# 370- AAC GCC ACC AAC CAC GCC ATC GTG CAG ACG CT - #G GTC CAC TTC ATC AAC1209Asn Ala Thr Asn His Ala Ile Val Gln Thr Le - #u Val His Phe Ile Asn# 385- CCG GAA ACG GTG CCC AAG CCC TGC TGT GCG CC - #C ACG CAG CTC AAT GCC1257Pro Glu Thr Val Pro Lys Pro Cys Cys Ala Pr - #o Thr Gln Leu Asn Ala# 400- ATC TCC GTC CTC TAC TTC GAT GAC AGC TCC AA - #C GTC ATC CTG AAG AAA1305Ile Ser Val Leu Tyr Phe Asp Asp Ser Ser As - #n Val Ile Leu Lys Lys# 415- TAC AGA AAC ATG GTG GTC CGG GCC TGT GGC TG - #C CAC TAGCTCCTCC1351Tyr Arg Asn Met Val Val Arg Ala Cys Gly Cy - #s His420 4 - #25 4 - #30- GAGAATTCAG ACCCTTTGGG GCCAAGTTTT TCTGGATCCT CCATTGCTCG CC - #TTGGCCAG1411- GAACCAGCAG ACCAACTGCC TTTTGTGAGA CCTTCCCCTC CCTATCCCCA AC - #TTTAAAGG1471- TGTGAGAGTA TTAGGAAACA TGAGCAGCAT ATGGCTTTTG ATCAGTTTTT CA - #GTGGCAGC1531- ATCCAATGAA CAAGATCCTA CAAGCTGTGC AGGCAAAACC TAGCAGGAAA AA - #AAAACAAC1591- GCATAAAGAA AAATGGCCGG GCCAGGTCAT TGGCTGGGAA GTCTCAGCCA TG - #CACGGACT1651- CGTTTCCAGA GGTAATTATG AGCGCCTACC AGCCAGGCCA CCCAGCCGTG GG - #AGGAAGGG1711- GGCGTGGCAA GGGGTGGGCA CATTGGTGTC TGTGCGAAAG GAAAATTGAC CC - #GGAAGTTC1771# 1822CACAATA AAACGAATGA ATGAAAAAAA AAAAAAAAAA A- (2) INFORMATION FOR SEQ ID NO:17:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 431 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:- Met His Val Arg Ser Leu Arg Ala Ala Ala Pr - #o His Ser Phe Val Ala# 15- Leu Trp Ala Pro Leu Phe Leu Leu Arg Ser Al - #a Leu Ala Asp Phe Ser# 30- Leu Asp Asn Glu Val His Ser Ser Phe Ile Hi - #s Arg Arg Leu Arg Ser# 45- Gln Glu Arg Arg Glu Met Gln Arg Glu Ile Le - #u Ser Ile Leu Gly Leu# 60- Pro His Arg Pro Arg Pro His Leu Gln Gly Ly - #s His Asn Ser Ala Pro# 80- Met Phe Met Leu Asp Leu Tyr Asn Ala Met Al - #a Val Glu Glu Gly Gly# 95- Gly Pro Gly Gly Gln Gly Phe Ser Tyr Pro Ty - #r Lys Ala Val Phe Ser# 110- Thr Gln Gly Pro Pro Leu Ala Ser Leu Gln As - #p Ser His Phe Leu Thr# 125- Asp Ala Asp Met Val Met Ser Phe Val Asn Le - #u Val Glu His Asp Lys# 140- Glu Phe Phe His Pro Arg Tyr His His Arg Gl - #u Phe Arg Phe Asp Leu145 1 - #50 1 - #55 1 -#60- Ser Lys Ile Pro Glu Gly Glu Ala Val Thr Al - #a Ala Glu Phe Arg Ile# 175- Tyr Lys Asp Tyr Ile Arg Glu Arg Phe Asp As - #n Glu Thr Phe Arg Ile# 190- Ser Val Tyr Gln Val Leu Gln Glu His Leu Gl - #y Arg Glu Ser Asp Leu# 205- Phe Leu Leu Asp Ser Arg Thr Leu Trp Ala Se - #r Glu Glu Gly Trp Leu# 220- Val Phe Asp Ile Thr Ala Thr Ser Asn His Tr - #p Val Val Asn Pro Arg225 2 - #30 2 - #35 2 -#40- His Asn Leu Gly Leu Gln Leu Ser Val Glu Th - #r Leu Asp Gly Gln Ser# 255- Ile Asn Pro Lys Leu Ala Gly Leu Ile Gly Ar - #g His Gly Pro Gln Asn# 270- Lys Gln Pro Phe Met Val Ala Phe Phe Lys Al - #a Thr Glu Val His Phe# 285- Arg Ser Ile Arg Ser Thr Gly Ser Lys Gln Ar - #g Ser Gln Asn Arg Ser# 300- Lys Thr Pro Lys Asn Gln Glu Ala Leu Arg Me - #t Ala Asn Val Ala Glu305 3 - #10 3 - #15 3 -#20- Asn Ser Ser Ser Asp Gln Arg Gln Ala Cys Ly - #s Lys His Glu Leu Tyr# 335- Val Ser Phe Arg Asp Leu Gly Trp Gln Asp Tr - #p Ile Ile Ala Pro Glu# 350- Gly Tyr Ala Ala Tyr Tyr Cys Glu Gly Glu Cy - #s Ala Phe Pro Leu Asn# 365- Ser Tyr Met Asn Ala Thr Asn His Ala Ile Va - #l Gln Thr Leu Val His# 380- Phe Ile Asn Pro Glu Thr Val Pro Lys Pro Cy - #s Cys Ala Pro Thr Gln385 3 - #90 3 - #95 4 -#00- Leu Asn Ala Ile Ser Val Leu Tyr Phe Asp As - #p Ser Ser Asn Val Ile# 415- Leu Lys Lys Tyr Arg Asn Met Val Val Arg Al - #a Cys Gly Cys His# 430- (2) INFORMATION FOR SEQ ID NO:18:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1873 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA- (iii) HYPOTHETICAL: NO- (iv) ANTI-SENSE: NO- (vi) ORIGINAL SOURCE: (A) ORGANISM: MURIDAE (F) TISSUE TYPE: EMBRYO- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 104..1393#/function= "OSTEOGENIC PROTEIN" /product=- # "MOP1"#"MOP1 (CDNA)" /note=- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18:- CTGCAGCAAG TGACCTCGGG TCGTGGACCG CTGCCCTGCC CCCTCCGCTG CC - #ACCTGGGG 60- CGGCGCGGGC CCGGTGCCCC GGATCGCGCG TAGAGCCGGC GCG ATG CA - #C GTG CGC 115# Met His Val Ar - #g# 1- TCG CTG CGC GCT GCG GCG CCA CAC AGC TTC GT - #G GCG CTC TGG GCG CCT 163Ser Leu Arg Ala Ala Ala Pro His Ser Phe Va - #l Ala Leu Trp Ala Pro# 20- CTG TTC TTG CTG CGC TCC GCC CTG GCC GAT TT - #C AGC CTG GAC AAC GAG 211Leu Phe Leu Leu Arg Ser Ala Leu Ala Asp Ph - #e Ser Leu Asp Asn Glu# 35- GTG CAC TCC AGC TTC ATC CAC CGG CGC CTC CG - #C AGC CAG GAG CGG CGG 259Val His Ser Ser Phe Ile His Arg Arg Leu Ar - #g Ser Gln Glu Arg Arg# 50- GAG ATG CAG CGG GAG ATC CTG TCC ATC TTA GG - #G TTG CCC CAT CGC CCG 307Glu Met Gln Arg Glu Ile Leu Ser Ile Leu Gl - #y Leu Pro His Arg Pro# 65- CGC CCG CAC CTC CAG GGA AAG CAT AAT TCG GC - #G CCC ATG TTC ATG TTG 355Arg Pro His Leu Gln Gly Lys His Asn Ser Al - #a Pro Met Phe Met Leu# 80- GAC CTG TAC AAC GCC ATG GCG GTG GAG GAG AG - #C GGG CCG GAC GGA CAG 403Asp Leu Tyr Asn Ala Met Ala Val Glu Glu Se - #r Gly Pro Asp Gly Gln#100- GGC TTC TCC TAC CCC TAC AAG GCC GTC TTC AG - #T ACC CAG GGC CCC CCT 451Gly Phe Ser Tyr Pro Tyr Lys Ala Val Phe Se - #r Thr Gln Gly Pro Pro# 115- TTA GCC AGC CTG CAG GAC AGC CAT TTC CTC AC - #T GAC GCC GAC ATG GTC 499Leu Ala Ser Leu Gln Asp Ser His Phe Leu Th - #r Asp Ala Asp Met Val# 130- ATG AGC TTC GTC AAC CTA GTG GAA CAT GAC AA - #A GAA TTC TTC CAC CCT 547Met Ser Phe Val Asn Leu Val Glu His Asp Ly - #s Glu Phe Phe His Pro# 145- CGA TAC CAC CAT CGG GAG TTC CGG TTT GAT CT - #T TCC AAG ATC CCC GAG 595Arg Tyr His His Arg Glu Phe Arg Phe Asp Le - #u Ser Lys Ile Pro Glu# 160- GGC GAA CGG GTG ACC GCA GCC GAA TTC AGG AT - #C TAT AAG GAC TAC ATC 643Gly Glu Arg Val Thr Ala Ala Glu Phe Arg Il - #e Tyr Lys Asp Tyr Ile165 1 - #70 1 - #75 1 -#80- CGG GAG CGA TTT GAC AAC GAG ACC TTC CAG AT - #C ACA GTC TAT CAG GTG 691Arg Glu Arg Phe Asp Asn Glu Thr Phe Gln Il - #e Thr Val Tyr Gln Val# 195- CTC CAG GAG CAC TCA GGC AGG GAG TCG GAC CT - #C TTC TTG CTG GAC AGC 739Leu Gln Glu His Ser Gly Arg Glu Ser Asp Le - #u Phe Leu Leu Asp Ser# 210- CGC ACC ATC TGG GCT TCT GAG GAG GGC TGG TT - #G GTG TTT GAT ATC ACA 787Arg Thr Ile Trp Ala Ser Glu Glu Gly Trp Le - #u Val Phe Asp Ile Thr# 225- GCC ACC AGC AAC CAC TGG GTG GTC AAC CCT CG - #G CAC AAC CTG GGC TTA 835Ala Thr Ser Asn His Trp Val Val Asn Pro Ar - #g His Asn Leu Gly Leu# 240- CAG CTC TCT GTG GAG ACC CTG GAT GGG CAG AG - #C ATC AAC CCC AAG TTG 883Gln Leu Ser Val Glu Thr Leu Asp Gly Gln Se - #r Ile Asn Pro Lys Leu245 2 - #50 2 - #55 2 -#60- GCA GGC CTG ATT GGA CGG CAT GGA CCC CAG AA - #C AAG CAA CCC TTC ATG 931Ala Gly Leu Ile Gly Arg His Gly Pro Gln As - #n Lys Gln Pro Phe Met# 275- GTG GCC TTC TTC AAG GCC ACG GAA GTC CAT CT - #C CGT AGT ATC CGG TCC 979Val Ala Phe Phe Lys Ala Thr Glu Val His Le - #u Arg Ser Ile Arg Ser# 290- ACG GGG GGC AAG CAG CGC AGC CAG AAT CGC TC - #C AAG ACG CCA AAG AAC1027Thr Gly Gly Lys Gln Arg Ser Gln Asn Arg Se - #r Lys Thr Pro Lys Asn# 305- CAA GAG GCC CTG AGG ATG GCC AGT GTG GCA GA - #A AAC AGC AGC AGT GAC1075Gln Glu Ala Leu Arg Met Ala Ser Val Ala Gl - #u Asn Ser Ser Ser Asp# 320- CAG AGG CAG GCC TGC AAG AAA CAT GAG CTG TA - #C GTC AGC TTC CGA GAC1123Gln Arg Gln Ala Cys Lys Lys His Glu Leu Ty - #r Val Ser Phe Arg Asp325 3 - #30 3 - #35 3 -#40- CTT GGC TGG CAG GAC TGG ATC ATT GCA CCT GA - #A GGC TAT GCT GCC TAC1171Leu Gly Trp Gln Asp Trp Ile Ile Ala Pro Gl - #u Gly Tyr Ala Ala Tyr# 355- TAC TGT GAG GGA GAG TGC GCC TTC CCT CTG AA - #C TCC TAC ATG AAC GCC1219Tyr Cys Glu Gly Glu Cys Ala Phe Pro Leu As - #n Ser Tyr Met Asn Ala# 370- ACC AAC CAC GCC ATC GTC CAG ACA CTG GTT CA - #C TTC ATC AAC CCA GAC1267Thr Asn His Ala Ile Val Gln Thr Leu Val Hi - #s Phe Ile Asn Pro Asp# 385- ACA GTA CCC AAG CCC TGC TGT GCG CCC ACC CA - #G CTC AAC GCC ATC TCT1315Thr Val Pro Lys Pro Cys Cys Ala Pro Thr Gl - #n Leu Asn Ala Ile Ser# 400- GTC CTC TAC TTC GAC GAC AGC TCT AAT GTC GA - #C CTG AAG AAG TAC AGA1363Val Leu Tyr Phe Asp Asp Ser Ser Asn Val As - #p Leu Lys Lys Tyr Arg405 4 - #10 4 - #15 4 -#20- AAC ATG GTG GTC CGG GCC TGT GGC TGC CAC TA - #GCTCTTCC TGAGACCCTG1413Asn Met Val Val Arg Ala Cys Gly Cys His# 430- ACCTTTGCGG GGCCACACCT TTCCAAATCT TCGATGTCTC ACCATCTAAG TC - #TCTCACTG1473- CCCACCTTGG CGAGGAGAAC AGACCAACCT CTCCTGAGCC TTCCCTCACC TC - #CCAACCGG1533- AAGCATGTAA GGGTTCCAGA AACCTGAGCG TGCAGCAGCT GATGAGCGCC CT - #TTCCTTCT1593- GGCACGTGAC GGACAAGATC CTACCAGCTA CCACAGCAAA CGCCTAAGAG CA - #GGAAAAAT1653- GTCTGCCAGG AAAGTGTCCA GTGTCCACAT GGCCCCTGGC GCTCTGAGTC TT - #TGAGGAGT1713- AATCGCAAGC CTCGTTCAGC TGCAGCAGAA GGAAGGGCTT AGCCAGGGTG GG - #CGCTGGCG1773- TCTGTGTTGA AGGGAAACCA AGCAGAAGCC ACTGTAATGA TATGTCACAA TA - #AAACCCAT1833# 1873 AAAA AAAAAAAAAA AAAAGAATTC- (2) INFORMATION FOR SEQ ID NO:19:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 430 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19:- Met His Val Arg Ser Leu Arg Ala Ala Ala Pr - #o His Ser Phe Val Ala# 15- Leu Trp Ala Pro Leu Phe Leu Leu Arg Ser Al - #a Leu Ala Asp Phe Ser# 30- Leu Asp Asn Glu Val His Ser Ser Phe Ile Hi - #s Arg Arg Leu Arg Ser# 45- Gln Glu Arg Arg Glu Met Gln Arg Glu Ile Le - #u Ser Ile Leu Gly Leu# 60- Pro His Arg Pro Arg Pro His Leu Gln Gly Ly - #s His Asn Ser Ala Pro# 80- Met Phe Met Leu Asp Leu Tyr Asn Ala Met Al - #a Val Glu Glu Ser Gly# 95- Pro Asp Gly Gln Gly Phe Ser Tyr Pro Tyr Ly - #s Ala Val Phe Ser Thr# 110- Gln Gly Pro Pro Leu Ala Ser Leu Gln Asp Se - #r His Phe Leu Thr Asp# 125- Ala Asp Met Val Met Ser Phe Val Asn Leu Va - #l Glu His Asp Lys Glu# 140- Phe Phe His Pro Arg Tyr His His Arg Glu Ph - #e Arg Phe Asp Leu Ser145 1 - #50 1 - #55 1 -#60- Lys Ile Pro Glu Gly Glu Arg Val Thr Ala Al - #a Glu Phe Arg Ile Tyr# 175- Lys Asp Tyr Ile Arg Glu Arg Phe Asp Asn Gl - #u Thr Phe Gln Ile Thr# 190- Val Tyr Gln Val Leu Gln Glu His Ser Gly Ar - #g Glu Ser Asp Leu Phe# 205- Leu Leu Asp Ser Arg Thr Ile Trp Ala Ser Gl - #u Glu Gly Trp Leu Val# 220- Phe Asp Ile Thr Ala Thr Ser Asn His Trp Va - #l Val Asn Pro Arg His225 2 - #30 2 - #35 2 -#40- Asn Leu Gly Leu Gln Leu Ser Val Glu Thr Le - #u Asp Gly Gln Ser Ile# 255- Asn Pro Lys Leu Ala Gly Leu Ile Gly Arg Hi - #s Gly Pro Gln Asn Lys# 270- Gln Pro Phe Met Val Ala Phe Phe Lys Ala Th - #r Glu Val His Leu Arg# 285- Ser Ile Arg Ser Thr Gly Gly Lys Gln Arg Se - #r Gln Asn Arg Ser Lys# 300- Thr Pro Lys Asn Gln Glu Ala Leu Arg Met Al - #a Ser Val Ala Glu Asn305 3 - #10 3 - #15 3 -#20- Ser Ser Ser Asp Gln Arg Gln Ala Cys Lys Ly - #s His Glu Leu Tyr Val# 335- Ser Phe Arg Asp Leu Gly Trp Gln Asp Trp Il - #e Ile Ala Pro Glu Gly# 350- Tyr Ala Ala Tyr Tyr Cys Glu Gly Glu Cys Al - #a Phe Pro Leu Asn Ser# 365- Tyr Met Asn Ala Thr Asn His Ala Ile Val Gl - #n Thr Leu Val His Phe# 380- Ile Asn Pro Asp Thr Val Pro Lys Pro Cys Cy - #s Ala Pro Thr Gln Leu385 3 - #90 3 - #95 4 -#00- Asn Ala Ile Ser Val Leu Tyr Phe Asp Asp Se - #r Ser Asn Val Asp Leu# 415- Lys Lys Tyr Arg Asn Met Val Val Arg Ala Cy - #s Gly Cys His# 430- (2) INFORMATION FOR SEQ ID NO:20:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1723 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens (F) TISSUE TYPE: HIPPOC - #AMPUS- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 490..1696#/function= "OSTEOGENIC PROTEIN" /product=- # "hOP2-PP"#"hOP2 (cDNA)" /note=- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20:- GGCGCCGGCA GAGCAGGAGT GGCTGGAGGA GCTGTGGTTG GAGCAGGAGG TG - #GCACGGCA 60- GGGCTGGAGG GCTCCCTATG AGTGGCGGAG ACGGCCCAGG AGGCGCTGGA GC - #AACAGCTC 120- CCACACCGCA CCAAGCGGTG GCTGCAGGAG CTCGCCCATC GCCCCTGCGC TG - #CTCGGACC 180- GCGGCCACAG CCGGACTGGC GGGTACGGCG GCGACAGAGG CATTGGCCGA GA - #GTCCCAGT 240- CCGCAGAGTA GCCCCGGCCT CGAGGCGGTG GCGTCCCGGT CCTCTCCGTC CA - #GGAGCCAG 300- GACAGGTGTC GCGCGGCGGG GCTCCAGGGA CCGCGCCTGA GGCCGGCTGC CC - #GCCCGTCC 360- CGCCCCGCCC CGCCGCCCGC CGCCCGCCGA GCCCAGCCTC CTTGCCGTCG GG - #GCGTCCCC 420- AGGCCCTGGG TCGGCCGCGG AGCCGATGCG CGCCCGCTGA GCGCCCCAGC TG - #AGCGCCCC 480- CGGCCTGCC ATG ACC GCG CTC CCC GGC CCG CTC TGG - # CTC CTG GGC CTG 528#Gly Pro Leu Trp Leu Leu Gly Leu# 10- GCG CTA TGC GCG CTG GGC GGG GGC GGC CCC GG - #C CTG CGA CCC CCG CCC 576Ala Leu Cys Ala Leu Gly Gly Gly Gly Pro Gl - #y Leu Arg Pro Pro Pro# 25- GGC TGT CCC CAG CGA CGT CTG GGC GCG CGC GA - #G CGC CGG GAC GTG CAG 624Gly Cys Pro Gln Arg Arg Leu Gly Ala Arg Gl - #u Arg Arg Asp Val Gln#40 45- CGC GAG ATC CTG GCG GTG CTC GGG CTG CCT GG - #G CGG CCC CGG CCC CGC 672Arg Glu Ile Leu Ala Val Leu Gly Leu Pro Gl - #y Arg Pro Arg Pro Arg# 60- GCG CCA CCC GCC GCC TCC CGG CTG CCC GCG TC - #C GCG CCG CTC TTC ATG 720Ala Pro Pro Ala Ala Ser Arg Leu Pro Ala Se - #r Ala Pro Leu Phe Met# 75- CTG GAC CTG TAC CAC GCC ATG GCC GGC GAC GA - #C GAC GAG GAC GGC GCG 768Leu Asp Leu Tyr His Ala Met Ala Gly Asp As - #p Asp Glu Asp Gly Ala# 90- CCC GCG GAG CGG CGC CTG GGC CGC GCC GAC CT - #G GTC ATG AGC TTC GTT 816Pro Ala Glu Arg Arg Leu Gly Arg Ala Asp Le - #u Val Met Ser Phe Val# 105- AAC ATG GTG GAG CGA GAC CGT GCC CTG GGC CA - #C CAG GAG CCC CAT TGG 864Asn Met Val Glu Arg Asp Arg Ala Leu Gly Hi - #s Gln Glu Pro His Trp110 1 - #15 1 - #20 1 -#25- AAG GAG TTC CGC TTT GAC CTG ACC CAG ATC CC - #G GCT GGG GAG GCG GTC 912Lys Glu Phe Arg Phe Asp Leu Thr Gln Ile Pr - #o Ala Gly Glu Ala Val# 140- ACA GCT GCG GAG TTC CGG ATT TAC AAG GTG CC - #C AGC ATC CAC CTG CTC 960Thr Ala Ala Glu Phe Arg Ile Tyr Lys Val Pr - #o Ser Ile His Leu Leu# 155- AAC AGG ACC CTC CAC GTC AGC ATG TTC CAG GT - #G GTC CAG GAG CAG TCC1008Asn Arg Thr Leu His Val Ser Met Phe Gln Va - #l Val Gln Glu Gln Ser# 170- AAC AGG GAG TCT GAC TTG TTC TTT TTG GAT CT - #T CAG ACG CTC CGA GCT1056Asn Arg Glu Ser Asp Leu Phe Phe Leu Asp Le - #u Gln Thr Leu Arg Ala# 185- GGA GAC GAG GGC TGG CTG GTG CTG GAT GTC AC - #A GCA GCC AGT GAC TGC1104Gly Asp Glu Gly Trp Leu Val Leu Asp Val Th - #r Ala Ala Ser Asp Cys190 1 - #95 2 - #00 2 -#05- TGG TTG CTG AAG CGT CAC AAG GAC CTG GGA CT - #C CGC CTC TAT GTG GAG1152Trp Leu Leu Lys Arg His Lys Asp Leu Gly Le - #u Arg Leu Tyr Val Glu# 220- ACT GAG GAC GGG CAC AGC GTG GAT CCT GGC CT - #G GCC GGC CTG CTG GGT1200Thr Glu Asp Gly His Ser Val Asp Pro Gly Le - #u Ala Gly Leu Leu Gly# 235- CAA CGG GCC CCA CGC TCC CAA CAG CCT TTC GT - #G GTC ACT TTC TTC AGG1248Gln Arg Ala Pro Arg Ser Gln Gln Pro Phe Va - #l Val Thr Phe Phe Arg# 250- GCC AGT CCG AGT CCC ATC CGC ACC CCT CGG GC - #A GTG AGG CCA CTG AGG1296Ala Ser Pro Ser Pro Ile Arg Thr Pro Arg Al - #a Val Arg Pro Leu Arg# 265- AGG AGG CAG CCG AAG AAA AGC AAC GAG CTG CC - #G CAG GCC AAC CGA CTC1344Arg Arg Gln Pro Lys Lys Ser Asn Glu Leu Pr - #o Gln Ala Asn Arg Leu270 2 - #75 2 - #80 2 -#85- CCA GGG ATC TTT GAT GAC GTC CAC GGC TCC CA - #C GGC CGG CAG GTC TGC1392Pro Gly Ile Phe Asp Asp Val His Gly Ser Hi - #s Gly Arg Gln Val Cys# 300- CGT CGG CAC GAG CTC TAC GTC AGC TTC CAG GA - #C CTC GGC TGG CTG GAC1440Arg Arg His Glu Leu Tyr Val Ser Phe Gln As - #p Leu Gly Trp Leu Asp# 315- TGG GTC ATC GCT CCC CAA GGC TAC TCG GCC TA - #T TAC TGT GAG GGG GAG1488Trp Val Ile Ala Pro Gln Gly Tyr Ser Ala Ty - #r Tyr Cys Glu Gly Glu# 330- TGC TCC TTC CCA CTG GAC TCC TGC ATG AAT GC - #C ACC AAC CAC GCC ATC1536Cys Ser Phe Pro Leu Asp Ser Cys Met Asn Al - #a Thr Asn His Ala Ile# 345- CTG CAG TCC CTG GTG CAC CTG ATG AAG CCA AA - #C GCA GTC CCC AAG GCG1584Leu Gln Ser Leu Val His Leu Met Lys Pro As - #n Ala Val Pro Lys Ala350 3 - #55 3 - #60 3 -#65- TGC TGT GCA CCC ACC AAG CTG AGC GCC ACC TC - #T GTG CTC TAC TAT GAC1632Cys Cys Ala Pro Thr Lys Leu Ser Ala Thr Se - #r Val Leu Tyr Tyr Asp# 380- AGC AGC AAC AAC GTC ATC CTG CGC AAA GCC CG - #C AAC ATG GTG GTC AAG1680Ser Ser Asn Asn Val Ile Leu Arg Lys Ala Ar - #g Asn Met Val Val Lys# 395- GCC TGC GGC TGC CAC T GAGTCAGCCC GCCCAGCCCT ACTG - #CAG#1723Ala Cys Gly Cys His 400- (2) INFORMATION FOR SEQ ID NO:21:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 402 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21:- Met Thr Ala Leu Pro Gly Pro Leu Trp Leu Le - #u Gly Leu Ala Leu Cys# 15- Ala Leu Gly Gly Gly Gly Pro Gly Leu Arg Pr - #o Pro Pro Gly Cys Pro# 30- Gln Arg Arg Leu Gly Ala Arg Glu Arg Arg As - #p Val Gln Arg Glu Ile# 45- Leu Ala Val Leu Gly Leu Pro Gly Arg Pro Ar - #g Pro Arg Ala Pro Pro# 60- Ala Ala Ser Arg Leu Pro Ala Ser Ala Pro Le - #u Phe Met Leu Asp Leu# 80- Tyr His Ala Met Ala Gly Asp Asp Asp Glu As - #p Gly Ala Pro Ala Glu# 95- Arg Arg Leu Gly Arg Ala Asp Leu Val Met Se - #r Phe Val Asn Met Val# 110- Glu Arg Asp Arg Ala Leu Gly His Gln Glu Pr - #o His Trp Lys Glu Phe# 125- Arg Phe Asp Leu Thr Gln Ile Pro Ala Gly Gl - #u Ala Val Thr Ala Ala# 140- Glu Phe Arg Ile Tyr Lys Val Pro Ser Ile Hi - #s Leu Leu Asn Arg Thr145 1 - #50 1 - #55 1 -#60- Leu His Val Ser Met Phe Gln Val Val Gln Gl - #u Gln Ser Asn Arg Glu# 175- Ser Asp Leu Phe Phe Leu Asp Leu Gln Thr Le - #u Arg Ala Gly Asp Glu# 190- Gly Trp Leu Val Leu Asp Val Thr Ala Ala Se - #r Asp Cys Trp Leu Leu# 205- Lys Arg His Lys Asp Leu Gly Leu Arg Leu Ty - #r Val Glu Thr Glu Asp# 220- Gly His Ser Val Asp Pro Gly Leu Ala Gly Le - #u Leu Gly Gln Arg Ala225 2 - #30 2 - #35 2 -#40- Pro Arg Ser Gln Gln Pro Phe Val Val Thr Ph - #e Phe Arg Ala Ser Pro# 255- Ser Pro Ile Arg Thr Pro Arg Ala Val Arg Pr - #o Leu Arg Arg Arg Gln# 270- Pro Lys Lys Ser Asn Glu Leu Pro Gln Ala As - #n Arg Leu Pro Gly Ile# 285- Phe Asp Asp Val His Gly Ser His Gly Arg Gl - #n Val Cys Arg Arg His# 300- Glu Leu Tyr Val Ser Phe Gln Asp Leu Gly Tr - #p Leu Asp Trp Val Ile305 3 - #10 3 - #15 3 -#20- Ala Pro Gln Gly Tyr Ser Ala Tyr Tyr Cys Gl - #u Gly Glu Cys Ser Phe# 335- Pro Leu Asp Ser Cys Met Asn Ala Thr Asn Hi - #s Ala Ile Leu Gln Ser# 350- Leu Val His Leu Met Lys Pro Asn Ala Val Pr - #o Lys Ala Cys Cys Ala# 365- Pro Thr Lys Leu Ser Ala Thr Ser Val Leu Ty - #r Tyr Asp Ser Ser Asn# 380- Asn Val Ile Leu Arg Lys Ala Arg Asn Met Va - #l Val Lys Ala Cys Gly385 3 - #90 3 - #95 4 -#00- Cys His- (2) INFORMATION FOR SEQ ID NO:22:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1926 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (vi) ORIGINAL SOURCE: (A) ORGANISM: MURIDAE (F) TISSUE TYPE: EMBRYO- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 93..1289#/function= "OSTEOGENIC PROTEIN" /product=- # "mOP2-PP"#"mOP2 cDNA" /note=- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22:- GCCAGGCACA GGTGCGCCGT CTGGTCCTCC CCGTCTGGCG TCAGCCGAGC CC - #GACCAGCT 60- ACCAGTGGAT GCGCGCCGGC TGAAAGTCCG AG ATG GCT ATG CGT - # CCC GGG CCA 113#Met Ala Met Arg Pro Gly Pro# 1 5- CTC TGG CTA TTG GGC CTT GCT CTG TGC GCG CT - #G GGA GGC GGC CAC GGT 161Leu Trp Leu Leu Gly Leu Ala Leu Cys Ala Le - #u Gly Gly Gly His Gly# 20- CCG CGT CCC CCG CAC ACC TGT CCC CAG CGT CG - #C CTG GGA GCG CGC GAG 209Pro Arg Pro Pro His Thr Cys Pro Gln Arg Ar - #g Leu Gly Ala Arg Glu# 35- CGC CGC GAC ATG CAG CGT GAA ATC CTG GCG GT - #G CTC GGG CTA CCG GGA 257Arg Arg Asp Met Gln Arg Glu Ile Leu Ala Va - #l Leu Gly Leu Pro Gly# 55- CGG CCC CGA CCC CGT GCA CAA CCC GCC GCT GC - #C CGG CAG CCA GCG TCC 305Arg Pro Arg Pro Arg Ala Gln Pro Ala Ala Al - #a Arg Gln Pro Ala Ser# 70- GCG CCC CTC TTC ATG TTG GAC CTA TAC CAC GC - #C ATG ACC GAT GAC GAC 353Ala Pro Leu Phe Met Leu Asp Leu Tyr His Al - #a Met Thr Asp Asp Asp# 85- GAC GGC GGG CCA CCA CAG GCT CAC TTA GGC CG - #T GCC GAC CTG GTC ATG 401Asp Gly Gly Pro Pro Gln Ala His Leu Gly Ar - #g Ala Asp Leu Val Met# 100- AGC TTC GTC AAC ATG GTG GAA CGC GAC CGT AC - #C CTG GGC TAC CAG GAG 449Ser Phe Val Asn Met Val Glu Arg Asp Arg Th - #r Leu Gly Tyr Gln Glu# 115- CCA CAC TGG AAG GAA TTC CAC TTT GAC CTA AC - #C CAG ATC CCT GCT GGG 497Pro His Trp Lys Glu Phe His Phe Asp Leu Th - #r Gln Ile Pro Ala Gly120 1 - #25 1 - #30 1 -#35- GAG GCT GTC ACA GCT GCT GAG TTC CGG ATC TA - #C AAA GAA CCC AGC ACC 545Glu Ala Val Thr Ala Ala Glu Phe Arg Ile Ty - #r Lys Glu Pro Ser Thr# 150- CAC CCG CTC AAC ACA ACC CTC CAC ATC AGC AT - #G TTC GAA GTG GTC CAA 593His Pro Leu Asn Thr Thr Leu His Ile Ser Me - #t Phe Glu Val Val Gln# 165- GAG CAC TCC AAC AGG GAG TCT GAC TTG TTC TT - #T TTG GAT CTT CAG ACG 641Glu His Ser Asn Arg Glu Ser Asp Leu Phe Ph - #e Leu Asp Leu Gln Thr# 180- CTC CGA TCT GGG GAC GAG GGC TGG CTG GTG CT - #G GAC ATC ACA GCA GCC 689Leu Arg Ser Gly Asp Glu Gly Trp Leu Val Le - #u Asp Ile Thr Ala Ala# 195- AGT GAC CGA TGG CTG CTG AAC CAT CAC AAG GA - #C CTG GGA CTC CGC CTC 737Ser Asp Arg Trp Leu Leu Asn His His Lys As - #p Leu Gly Leu Arg Leu200 2 - #05 2 - #10 2 -#15- TAT GTG GAA ACC GCG GAT GGG CAC AGC ATG GA - #T CCT GGC CTG GCT GGT 785Tyr Val Glu Thr Ala Asp Gly His Ser Met As - #p Pro Gly Leu Ala Gly# 230- CTG CTT GGA CGA CAA GCA CCA CGC TCC AGA CA - #G CCT TTC ATG GTA ACC 833Leu Leu Gly Arg Gln Ala Pro Arg Ser Arg Gl - #n Pro Phe Met Val Thr# 245- TTC TTC AGG GCC AGC CAG AGT CCT GTG CGG GC - #C CCT CGG GCA GCG AGA 881Phe Phe Arg Ala Ser Gln Ser Pro Val Arg Al - #a Pro Arg Ala Ala Arg# 260- CCA CTG AAG AGG AGG CAG CCA AAG AAA ACG AA - #C GAG CTT CCG CAC CCC 929Pro Leu Lys Arg Arg Gln Pro Lys Lys Thr As - #n Glu Leu Pro His Pro# 275- AAC AAA CTC CCA GGG ATC TTT GAT GAT GGC CA - #C GGT TCC CGC GGC AGA 977Asn Lys Leu Pro Gly Ile Phe Asp Asp Gly Hi - #s Gly Ser Arg Gly Arg280 2 - #85 2 - #90 2 -#95- GAG GTT TGC CGC AGG CAT GAG CTC TAC GTC AG - #C TTC CGT GAC CTT GGC1025Glu Val Cys Arg Arg His Glu Leu Tyr Val Se - #r Phe Arg Asp Leu Gly# 310- TGG CTG GAC TGG GTC ATC GCC CCC CAG GGC TA - #C TCT GCC TAT TAC TGT1073Trp Leu Asp Trp Val Ile Ala Pro Gln Gly Ty - #r Ser Ala Tyr Tyr Cys# 325- GAG GGG GAG TGT GCT TTC CCA CTG GAC TCC TG - #T ATG AAC GCC ACC AAC1121Glu Gly Glu Cys Ala Phe Pro Leu Asp Ser Cy - #s Met Asn Ala Thr Asn# 340- CAT GCC ATC TTG CAG TCT CTG GTG CAC CTG AT - #G AAG CCA GAT GTT GTC1169His Ala Ile Leu Gln Ser Leu Val His Leu Me - #t Lys Pro Asp Val Val# 355- CCC AAG GCA TGC TGT GCA CCC ACC AAA CTG AG - #T GCC ACC TCT GTG CTG1217Pro Lys Ala Cys Cys Ala Pro Thr Lys Leu Se - #r Ala Thr Ser Val Leu360 3 - #65 3 - #70 3 -#75- TAC TAT GAC AGC AGC AAC AAT GTC ATC CTG CG - #T AAA CAC CGT AAC ATG1265Tyr Tyr Asp Ser Ser Asn Asn Val Ile Leu Ar - #g Lys His Arg Asn Met# 390- GTG GTC AAG GCC TGT GGC TGC CAC TGAGGCCCCG CC - #CAGCATCC TGCTTCTACT1319Val Val Lys Ala Cys Gly Cys His 395- ACCTTACCAT CTGGCCGGGC CCCTCTCCAG AGGCAGAAAC CCTTCTATGT TA - #TCATAGCT1379- CAGACAGGGG CAATGGGAGG CCCTTCACTT CCCCTGGCCA CTTCCTGCTA AA - #ATTCTGGT1439- CTTTCCCAGT TCCTCTGTCC TTCATGGGGT TTCGGGGCTA TCACCCCGCC CT - #CTCCATCC1499- TCCTACCCCA AGCATAGACT GAATGCACAC AGCATCCCAG AGCTATGCTA AC - #TGAGAGGT1559- CTGGGGTCAG CACTGAAGGC CCACATGAGG AAGACTGATC CTTGGCCATC CT - #CAGCCCAC1619- AATGGCAAAT TCTGGATGGT CTAAGAAGGC CCTGGAATTC TAAACTAGAT GA - #TCTGGGCT1679- CTCTGCACCA TTCATTGTGG CAGTTGGGAC ATTTTTAGGT ATAACAGACA CA - #TACACTTA1739- GATCAATGCA TCGCTGTACT CCTTGAAATC AGAGCTAGCT TGTTAGAAAA AG - #AATCAGAG1799- CCAGGTATAG CGGTGCATGT CATTAATCCC AGCGCTAAAG AGACAGAGAC AG - #GAGAATCT1859- CTGTGAGTTC AAGGCCACAT AGAAAGAGCC TGTCTCGGGA GCAGGAAAAA AA - #AAAAAAAC1919# 1926- (2) INFORMATION FOR SEQ ID NO:23:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 399 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23:- Met Ala Met Arg Pro Gly Pro Leu Trp Leu Le - #u Gly Leu Ala Leu Cys# 15- Ala Leu Gly Gly Gly His Gly Pro Arg Pro Pr - #o His Thr Cys Pro Gln# 30- Arg Arg Leu Gly Ala Arg Glu Arg Arg Asp Me - #t Gln Arg Glu Ile Leu# 45- Ala Val Leu Gly Leu Pro Gly Arg Pro Arg Pr - #o Arg Ala Gln Pro Ala# 60- Ala Ala Arg Gln Pro Ala Ser Ala Pro Leu Ph - #e Met Leu Asp Leu Tyr# 80- His Ala Met Thr Asp Asp Asp Asp Gly Gly Pr - #o Pro Gln Ala His Leu# 95- Gly Arg Ala Asp Leu Val Met Ser Phe Val As - #n Met Val Glu Arg Asp# 110- Arg Thr Leu Gly Tyr Gln Glu Pro His Trp Ly - #s Glu Phe His Phe Asp# 125- Leu Thr Gln Ile Pro Ala Gly Glu Ala Val Th - #r Ala Ala Glu Phe Arg# 140- Ile Tyr Lys Glu Pro Ser Thr His Pro Leu As - #n Thr Thr Leu His Ile145 1 - #50 1 - #55 1 -#60- Ser Met Phe Glu Val Val Gln Glu His Ser As - #n Arg Glu Ser Asp Leu# 175- Phe Phe Leu Asp Leu Gln Thr Leu Arg Ser Gl - #y Asp Glu Gly Trp Leu# 190- Val Leu Asp Ile Thr Ala Ala Ser Asp Arg Tr - #p Leu Leu Asn His His# 205- Lys Asp Leu Gly Leu Arg Leu Tyr Val Glu Th - #r Ala Asp Gly His Ser# 220- Met Asp Pro Gly Leu Ala Gly Leu Leu Gly Ar - #g Gln Ala Pro Arg Ser225 2 - #30 2 - #35 2 -#40- Arg Gln Pro Phe Met Val Thr Phe Phe Arg Al - #a Ser Gln Ser Pro Val# 255- Arg Ala Pro Arg Ala Ala Arg Pro Leu Lys Ar - #g Arg Gln Pro Lys Lys# 270- Thr Asn Glu Leu Pro His Pro Asn Lys Leu Pr - #o Gly Ile Phe Asp Asp# 285- Gly His Gly Ser Arg Gly Arg Glu Val Cys Ar - #g Arg His Glu Leu Tyr# 300- Val Ser Phe Arg Asp Leu Gly Trp Leu Asp Tr - #p Val Ile Ala Pro Gln305 3 - #10 3 - #15 3 -#20- Gly Tyr Ser Ala Tyr Tyr Cys Glu Gly Glu Cy - #s Ala Phe Pro Leu Asp# 335- Ser Cys Met Asn Ala Thr Asn His Ala Ile Le - #u Gln Ser Leu Val His# 350- Leu Met Lys Pro Asp Val Val Pro Lys Ala Cy - #s Cys Ala Pro Thr Lys# 365- Leu Ser Ala Thr Ser Val Leu Tyr Tyr Asp Se - #r Ser Asn Asn Val Ile# 380- Leu Arg Lys His Arg Asn Met Val Val Lys Al - #a Cys Gly Cys His385 3 - #90 3 - #95- (2) INFORMATION FOR SEQ ID NO:24:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1368 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..1368- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24:- ATG TCG GGA CTG CGA AAC ACC TCG GAG GCC GT - #T GCA GTG CTC GCC TCC 48Met Ser Gly Leu Arg Asn Thr Ser Glu Ala Va - #l Ala Val Leu Ala Ser# 15- CTG GGA CTC GGA ATG GTT CTG CTC ATG TTC GT - #G GCG ACC ACG CCG CCG 96Leu Gly Leu Gly Met Val Leu Leu Met Phe Va - #l Ala Thr Thr Pro Pro# 30- GCC GTT GAG GCC ACC CAG TCG GGG ATT TAC AT - #A GAC AAC GGC AAG GAC 144Ala Val Glu Ala Thr Gln Ser Gly Ile Tyr Il - #e Asp Asn Gly Lys Asp# 45- CAG ACG ATC ATG CAC AGA GTG CTG AGC GAG GA - #C GAC AAG CTG GAC GTC 192Gln Thr Ile Met His Arg Val Leu Ser Glu As - #p Asp Lys Leu Asp Val# 60- TCG TAC GAG ATC CTC GAG TTC CTG GGC ATC GC - #C GAA CGG CCG ACG CAC 240Ser Tyr Glu Ile Leu Glu Phe Leu Gly Ile Al - #a Glu Arg Pro Thr His# 80- CTG AGC AGC CAC CAG TTG TCG CTG AGG AAG TC - #G GCT CCC AAG TTC CTG 288Leu Ser Ser His Gln Leu Ser Leu Arg Lys Se - #r Ala Pro Lys Phe Leu# 95- CTG GAC GTC TAC CAC CGC ATC ACG GCG GAG GA - #G GGT CTC AGC GAT CAG 336Leu Asp Val Tyr His Arg Ile Thr Ala Glu Gl - #u Gly Leu Ser Asp Gln# 110- GAT GAG GAC GAC GAC TAC GAA CGC GGC CAT CG - #G TCC AGG AGG AGC GCC 384Asp Glu Asp Asp Asp Tyr Glu Arg Gly His Ar - #g Ser Arg Arg Ser Ala# 125- GAC CTC GAG GAG GAT GAG GGC GAG CAG CAG AA - #G AAC TTC ATC ACC GAC 432Asp Leu Glu Glu Asp Glu Gly Glu Gln Gln Ly - #s Asn Phe Ile Thr Asp# 140- CTG GAC AAG CGG GCC ATC GAC GAG AGC GAC AT - #C ATC ATG ACC TTC CTG 480Leu Asp Lys Arg Ala Ile Asp Glu Ser Asp Il - #e Ile Met Thr Phe Leu145 1 - #50 1 - #55 1 -#60- AAC AAG CGC CAC CAC AAT GTG GAC GAA CTG CG - #T CAC GAG CAC GGC CGT 528Asn Lys Arg His His Asn Val Asp Glu Leu Ar - #g His Glu His Gly Arg# 175- CGC CTG TGG TTC GAC GTC TCC AAC GTG CCC AA - #C GAC AAC TAC CTG GTG 576Arg Leu Trp Phe Asp Val Ser Asn Val Pro As - #n Asp Asn Tyr Leu Val# 190- ATG GCC GAG CTG CGC ATC TAT CAG AAC GCC AA - #C GAG GGC AAG TGG CTG 624Met Ala Glu Leu Arg Ile Tyr Gln Asn Ala As - #n Glu Gly Lys Trp Leu# 205- ACC GCC AAC AGG GAG TTC ACC ATC ACG GTA TA - #C GCC ATT GGC ACC GGC 672Thr Ala Asn Arg Glu Phe Thr Ile Thr Val Ty - #r Ala Ile Gly Thr Gly# 220- ACG CTG GGC CAG CAC ACC ATG GAG CCG CTG TC - #C TCG GTG AAC ACC ACC 720Thr Leu Gly Gln His Thr Met Glu Pro Leu Se - #r Ser Val Asn Thr Thr225 2 - #30 2 - #35 2 -#40- GGG GAC TAC GTG GGC TGG TTG GAG CTC AAC GT - #G ACC GAG GGC CTG CAC 768Gly Asp Tyr Val Gly Trp Leu Glu Leu Asn Va - #l Thr Glu Gly Leu His# 255- GAG TGG CTG GTC AAG TCG AAG GAC AAT CAT GG - #C ATC TAC ATT GGA GCA 816Glu Trp Leu Val Lys Ser Lys Asp Asn His Gl - #y Ile Tyr Ile Gly Ala# 270- CAC GCT GTC AAC CGA CCC GAC CGC GAG GTG AA - #G CTG GAC GAC ATT GGA 864His Ala Val Asn Arg Pro Asp Arg Glu Val Ly - #s Leu Asp Asp Ile Gly# 285- CTG ATC CAC CGC AAG GTG GAC GAC GAG TTC CA - #G CCC TTC ATG ATC GGC 912Leu Ile His Arg Lys Val Asp Asp Glu Phe Gl - #n Pro Phe Met Ile Gly# 300- TTC TTC CGC GGA CCG GAG CTG ATC AAG GCG AC - #G GCC CAC AGC AGC CAC 960Phe Phe Arg Gly Pro Glu Leu Ile Lys Ala Th - #r Ala His Ser Ser His305 3 - #10 3 - #15 3 -#20- CAC AGG AGC AAG CGA AGC GCC AGC CAT CCA CG - #C AAG CGC AAG AAG TCG1008His Arg Ser Lys Arg Ser Ala Ser His Pro Ar - #g Lys Arg Lys Lys Ser# 335- GTG TCG CCC AAC AAC GTG CCG CTG CTG GAA CC - #G ATG GAG AGC ACG CGC1056Val Ser Pro Asn Asn Val Pro Leu Leu Glu Pr - #o Met Glu Ser Thr Arg# 350- AGC TGC CAG ATG CAG ACC CTG TAC ATA GAC TT - #C AAG GAT CTG GGC TGG1104Ser Cys Gln Met Gln Thr Leu Tyr Ile Asp Ph - #e Lys Asp Leu Gly Trp# 365- CAT GAC TGG ATC ATC GCA CCA GAG GGC TAT GG - #C GCC TTC TAC TGC AGC1152His Asp Trp Ile Ile Ala Pro Glu Gly Tyr Gl - #y Ala Phe Tyr Cys Ser# 380- GGC GAG TGC AAT TTC CCG CTC AAT GCG CAC AT - #G AAC GCC ACG AAC CAT1200Gly Glu Cys Asn Phe Pro Leu Asn Ala His Me - #t Asn Ala Thr Asn His385 3 - #90 3 - #95 4 -#00- GCG ATC GTC CAG ACC CTG GTC CAC CTG CTG GA - #G CCC AAG AAG GTG CCC1248Ala Ile Val Gln Thr Leu Val His Leu Leu Gl - #u Pro Lys Lys Val Pro# 415- AAG CCC TGC TGC GCT CCG ACC AGG CTG GGA GC - #A CTA CCC GTT CTG TAC1296Lys Pro Cys Cys Ala Pro Thr Arg Leu Gly Al - #a Leu Pro Val Leu Tyr# 430- CAC CTG AAC GAC GAG AAT GTG AAC CTG AAA AA - #G TAT AGA AAC ATG ATT1344His Leu Asn Asp Glu Asn Val Asn Leu Lys Ly - #s Tyr Arg Asn Met Ile# 445# 1368GG TGC CAT TGAVal Lys Ser Cys Gly Cys His# 455- (2) INFORMATION FOR SEQ ID NO:25:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 455 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:25:- Met Ser Gly Leu Arg Asn Thr Ser Glu Ala Va - #l Ala Val Leu Ala Ser# 15- Leu Gly Leu Gly Met Val Leu Leu Met Phe Va - #l Ala Thr Thr Pro Pro# 30- Ala Val Glu Ala Thr Gln Ser Gly Ile Tyr Il - #e Asp Asn Gly Lys Asp# 45- Gln Thr Ile Met His Arg Val Leu Ser Glu As - #p Asp Lys Leu Asp Val# 60- Ser Tyr Glu Ile Leu Glu Phe Leu Gly Ile Al - #a Glu Arg Pro Thr His# 80- Leu Ser Ser His Gln Leu Ser Leu Arg Lys Se - #r Ala Pro Lys Phe Leu# 95- Leu Asp Val Tyr His Arg Ile Thr Ala Glu Gl - #u Gly Leu Ser Asp Gln# 110- Asp Glu Asp Asp Asp Tyr Glu Arg Gly His Ar - #g Ser Arg Arg Ser Ala# 125- Asp Leu Glu Glu Asp Glu Gly Glu Gln Gln Ly - #s Asn Phe Ile Thr Asp# 140- Leu Asp Lys Arg Ala Ile Asp Glu Ser Asp Il - #e Ile Met Thr Phe Leu145 1 - #50 1 - #55 1 -#60- Asn Lys Arg His His Asn Val Asp Glu Leu Ar - #g His Glu His Gly Arg# 175- Arg Leu Trp Phe Asp Val Ser Asn Val Pro As - #n Asp Asn Tyr Leu Val# 190- Met Ala Glu Leu Arg Ile Tyr Gln Asn Ala As - #n Glu Gly Lys Trp Leu# 205- Thr Ala Asn Arg Glu Phe Thr Ile Thr Val Ty - #r Ala Ile Gly Thr Gly# 220- Thr Leu Gly Gln His Thr Met Glu Pro Leu Se - #r Ser Val Asn Thr Thr225 2 - #30 2 - #35 2 -#40- Gly Asp Tyr Val Gly Trp Leu Glu Leu Asn Va - #l Thr Glu Gly Leu His# 255- Glu Trp Leu Val Lys Ser Lys Asp Asn His Gl - #y Ile Tyr Ile Gly Ala# 270- His Ala Val Asn Arg Pro Asp Arg Glu Val Ly - #s Leu Asp Asp Ile Gly# 285- Leu Ile His Arg Lys Val Asp Asp Glu Phe Gl - #n Pro Phe Met Ile Gly# 300- Phe Phe Arg Gly Pro Glu Leu Ile Lys Ala Th - #r Ala His Ser Ser His305 3 - #10 3 - #15 3 -#20- His Arg Ser Lys Arg Ser Ala Ser His Pro Ar - #g Lys Arg Lys Lys Ser# 335- Val Ser Pro Asn Asn Val Pro Leu Leu Glu Pr - #o Met Glu Ser Thr Arg# 350- Ser Cys Gln Met Gln Thr Leu Tyr Ile Asp Ph - #e Lys Asp Leu Gly Trp# 365- His Asp Trp Ile Ile Ala Pro Glu Gly Tyr Gl - #y Ala Phe Tyr Cys Ser# 380- Gly Glu Cys Asn Phe Pro Leu Asn Ala His Me - #t Asn Ala Thr Asn His385 3 - #90 3 - #95 4 -#00- Ala Ile Val Gln Thr Leu Val His Leu Leu Gl - #u Pro Lys Lys Val Pro# 415- Lys Pro Cys Cys Ala Pro Thr Arg Leu Gly Al - #a Leu Pro Val Leu Tyr# 430- His Leu Asn Asp Glu Asn Val Asn Leu Lys Ly - #s Tyr Arg Asn Met Ile# 445- Val Lys Ser Cys Gly Cys His# 455- (2) INFORMATION FOR SEQ ID NO:26:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 104 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..104#/note= "BMP3"OTHER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:26:- Cys Ala Arg Arg Tyr Leu Lys Val Asp Phe Al - #a Asp Ile Gly Trp Ser# 15- Glu Trp Ile Ile Ser Pro Lys Ser Phe Asp Al - #a Tyr Tyr Cys Ser Gly# 30- Ala Cys Gln Phe Pro Met Pro Lys Ser Leu Ly - #s Pro Ser Asn His Ala# 45- Thr Ile Gln Ser Ile Val Ala Arg Ala Val Gl - #y Val Val Pro Gly Ile# 60- Pro Glu Pro Cys Cys Val Pro Glu Lys Met Se - #r Ser Leu Ser Ile Leu# 80- Phe Phe Asp Glu Asn Lys Asn Val Val Leu Ly - #s Val Tyr Pro Asn Met# 95- Thr Val Glu Ser Cys Ala Cys Arg 100- (2) INFORMATION FOR SEQ ID NO:27:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: HOMO SAPI - #ENS- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..102#/note= "BMP5"OTHER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:27:- Cys Lys Lys His Glu Leu Tyr Val Ser Phe Ar - #g Asp Leu Gly Trp Gln# 15- Asp Trp Ile Ile Ala Pro Glu Gly Tyr Ala Al - #a Phe Tyr Cys Asp Gly# 30- Glu Cys Ser Phe Pro Leu Asn Ala His Met As - #n Ala Thr Asn His Ala# 45- Ile Val Gln Thr Leu Val His Leu Met Phe Pr - #o Asp His Val Pro Lys# 60- Pro Cys Cys Ala Pro Thr Lys Leu Asn Ala Il - #e Ser Val Leu Tyr Phe# 80- Asp Asp Ser Ser Asn Val Ile Leu Lys Lys Ty - #r Arg Asn Met Val Val# 95- Arg Ser Cys Gly Cys His 100- (2) INFORMATION FOR SEQ ID NO:28:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (vi) ORIGINAL SOURCE: (A) ORGANISM: HOMO SAPI - #ENS- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..102#/note= "BMP6"OTHER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:28:- Cys Arg Lys His Glu Leu Tyr Val Ser Phe Gl - #n Asp Leu Gly Trp Gln# 15- Asp Trp Ile Ile Ala Pro Lys Gly Tyr Ala Al - #a Asn Tyr Cys Asp Gly# 30- Glu Cys Ser Phe Pro Leu Asn Ala His Met As - #n Ala Thr Asn His Ala# 45- Ile Val Gln Thr Leu Val His Leu Met Asn Pr - #o Glu Tyr Val Pro Lys# 60- Pro Cys Cys Ala Pro Thr Lys Leu Asn Ala Il - #e Ser Val Leu Tyr Phe# 80- Asp Asp Asn Ser Asn Val Ile Leu Lys Lys Ty - #r Arg Trp Met Val Val# 95- Arg Ala Cys Gly Cys His 100- (2) INFORMATION FOR SEQ ID NO:29:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..102#/label= OPX) OTHER INFORMATION:#"WHEREIN EACH XAA IS INDEPENDENTLY SELECTED#GROUP OF ONE OR MORE SPECIFIED AMINO ACIDS AS DEFINE - #D IN THE SPECIFICATION (SECTION II.B.2.)"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:29:- Cys Xaa Xaa His Glu Leu Tyr Val Xaa Phe Xa - #a Asp Leu Gly Trp Xaa# 15- Asp Trp Xaa Ile Ala Pro Xaa Gly Tyr Xaa Al - #a Tyr Tyr Cys Glu Gly# 30- Glu Cys Xaa Phe Pro Leu Xaa Ser Xaa Met As - #n Ala Thr Asn His Ala# 45- Ile Xaa Gln Xaa Leu Val His Xaa Xaa Xaa Pr - #o Xaa Xaa Val Pro Lys# 60- Xaa Cys Cys Ala Pro Thr Xaa Leu Xaa Ala Xa - #a Ser Val Leu Tyr Xaa#80- Asp Xaa Ser Xaa Asn Val Xaa Leu Xaa Lys Xa - #a Arg Asn Met Val Val# 95- Xaa Ala Cys Gly Cys His 100- (2) INFORMATION FOR SEQ ID NO:30:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 97 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..97#/label= GENERIC-SEQ5NFORMATION:#"WHEREIN EACH XAA IS INDEPENDENTLY SELECTED#GROUP OF ONE OR MORE SPECIFIED AMINO ACIDS AS DEFINE - #D IN THE SPECIFICATION."- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:30:- Leu Xaa Xaa Xaa Phe Xaa Xaa Xaa Gly Trp Xa - #a Xaa Trp Xaa Xaa Xaa# 15- Pro Xaa Xaa Xaa Xaa Ala Xaa Tyr Cys Xaa Gl - #y Xaa Cys Xaa Xaa Pro# 30- Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Asn His Al - #a Xaa Xaa Xaa Xaa Xaa# 45- Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Cys Cys Xaa Pro# 60- Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Leu Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa# 80- Val Xaa Leu Xaa Xaa Xaa Xaa Xaa Met Xaa Va - #l Xaa Xaa Cys Xaa Cys# 95- Xaa- (2) INFORMATION FOR SEQ ID NO:31:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 102 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: Protein (B) LOCATION: 1..102#/label= GENERIC-SEQ6NFORMATION:#"WHEREIN EACH XAA IS INDEPENDENTLY SELECTED#GROUP OF ONE OR MORE SPECIFIED AMINO ACIDS AS DEFINE - #D IN THE SPECIFICATION. "- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:31:- Cys Xaa Xaa Xaa Xaa Leu Xaa Xaa Xaa Phe Xa - #a Xaa Xaa Gly Trp Xaa# 15- Xaa Trp Xaa Xaa Xaa Pro Xaa Xaa Xaa Xaa Al - #a Xaa Tyr Cys Xaa Gly# 30- Xaa Cys Xaa Xaa Pro Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Asn His Ala# 45- Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa# 60- Xaa Cys Cys Xaa Pro Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Leu Xaa Xaa# 80- Xaa Xaa Xaa Xaa Xaa Val Xaa Leu Xaa Xaa Xa - #a Xaa Xaa Met Xaa Val# 95- Xaa Xaa Cys Xaa Cys Xaa 100- (2) INFORMATION FOR SEQ ID NO:32:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1247 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA- (vi) ORIGINAL SOURCE: (A) ORGANISM: HOMO SAPI - #ENS (F) TISSUE TYPE: BRAIN- (ix) FEATURE: (A) NAME/KEY: CDS- (B) LOCATION: 84..1199#/product= "GDF-1"R INFORMATION:#"GDF-1 CDNA" /note=- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:32:- GGGGACACCG GCCCCGCCCT CAGCCCACTG GTCCCGGGCC GCCGCGGACC CT - #GCGCACTC 60- TCTGGTCATC GCCTGGGAGG AAG ATG CCA CCG CCG CAG CA - #A GGT CCC TGC 110#Gly Pro Cys Pro Pro Pro Gln Gln# 5 1- GGC CAC CAC CTC CTC CTC CTC CTG GCC CTG CT - #G CTG CCC TCG CTG CCC 158Gly His His Leu Leu Leu Leu Leu Ala Leu Le - #u Leu Pro Ser Leu Pro# 25- CTG ACC CGC GCC CCC GTG CCC CCA GGC CCA GC - #C GCC GCC CTG CTC CAG 206Leu Thr Arg Ala Pro Val Pro Pro Gly Pro Al - #a Ala Ala Leu Leu Gln# 40- GCT CTA GGA CTG CGC GAT GAG CCC CAG GGT GC - #C CCC AGG CTC CGG CCG 254Ala Leu Gly Leu Arg Asp Glu Pro Gln Gly Al - #a Pro Arg Leu Arg Pro# 55- GTT CCC CCG GTC ATG TGG CGC CTG TTT CGA CG - #C CGG GAC CCC CAG GAG 302Val Pro Pro Val Met Trp Arg Leu Phe Arg Ar - #g Arg Asp Pro Gln Glu# 70- ACC AGG TCT GGC TCG CGG CGG ACG TCC CCA GG - #G GTC ACC CTG CAA CCG 350Thr Arg Ser Gly Ser Arg Arg Thr Ser Pro Gl - #y Val Thr Leu Gln Pro# 85- TGC CAC GTG GAG GAG CTG GGG GTC GCC GGA AA - #C ATC GTG CGC CAC ATC 398Cys His Val Glu Glu Leu Gly Val Ala Gly As - #n Ile Val Arg His Ile#105- CCG GAC CGC GGT GCG CCC ACC CGG GCC TCG GA - #G CCT GTC TCG GCC GCG 446Pro Asp Arg Gly Ala Pro Thr Arg Ala Ser Gl - #u Pro Val Ser Ala Ala# 120- GGG CAT TGC CCT GAG TGG ACA GTC GTC TTC GA - #C CTG TCG GCT GTG GAA 494Gly His Cys Pro Glu Trp Thr Val Val Phe As - #p Leu Ser Ala Val Glu# 135- CCC GCT GAG CGC CCG AGC CGG GCC CGC CTG GA - #G CTG CGT TTC GCG GCG 542Pro Ala Glu Arg Pro Ser Arg Ala Arg Leu Gl - #u Leu Arg Phe Ala Ala# 150- GCG GCG GCG GCA GCC CCG GAG GGC GGC TGG GA - #G CTG AGC GTG GCG CAA 590Ala Ala Ala Ala Ala Pro Glu Gly Gly Trp Gl - #u Leu Ser Val Ala Gln# 165- GCG GGC CAG GGC GCG GGC GCG GAC CCC GGG CC - #G GTG CTG CTC CGC CAG 638Ala Gly Gln Gly Ala Gly Ala Asp Pro Gly Pr - #o Val Leu Leu Arg Gln170 1 - #75 1 - #80 1 -#85- TTG GTG CCC GCC CTG GGG CCG CCA GTG CGC GC - #G GAG CTG CTG GGC GCC 686Leu Val Pro Ala Leu Gly Pro Pro Val Arg Al - #a Glu Leu Leu Gly Ala# 200- GCT TGG GCT CGC AAC GCC TCA TGG CCG CGC AG - #C CTC CGC CTG GCG CTG 734Ala Trp Ala Arg Asn Ala Ser Trp Pro Arg Se - #r Leu Arg Leu Ala Leu# 215- GCG CTA CGC CCC CGG GCC CCT GCC GCC TGC GC - #G CGC CTG GCC GAG GCC 782Ala Leu Arg Pro Arg Ala Pro Ala Ala Cys Al - #a Arg Leu Ala Glu Ala# 230- TCG CTG CTG CTG GTG ACC CTC GAC CCG CGC CT - #G TGC CAC CCC CTG GCC 830Ser Leu Leu Leu Val Thr Leu Asp Pro Arg Le - #u Cys His Pro Leu Ala# 245- CGG CCG CGG CGC GAC GCC GAA CCC GTG TTG GG - #C GGC GGC CCC GGG GGC 878Arg Pro Arg Arg Asp Ala Glu Pro Val Leu Gl - #y Gly Gly Pro Gly Gly250 2 - #55 2 - #60 2 -#65- GCT TGT CGC GCG CGG CGG CTG TAC GTG AGC TT - #C CGC GAG GTG GGC TGG 926Ala Cys Arg Ala Arg Arg Leu Tyr Val Ser Ph - #e Arg Glu Val Gly Trp# 280- CAC CGC TGG GTC ATC GCG CCG CGC GGC TTC CT - #G GCC AAC TAC TGC CAG 974His Arg Trp Val Ile Ala Pro Arg Gly Phe Le - #u Ala Asn Tyr Cys Gln# 295- GGT CAG TGC GCG CTG CCC GTC GCG CTG TCG GG - #G TCC GGG GGG CCG CCG1022Gly Gln Cys Ala Leu Pro Val Ala Leu Ser Gl - #y Ser Gly Gly Pro Pro# 310- GCG CTC AAC CAC GCT GTG CTG CGC GCG CTC AT - #G CAC GCG GCC GCC CCG1070Ala Leu Asn His Ala Val Leu Arg Ala Leu Me - #t His Ala Ala Ala Pro# 325- GGA GCC GCC GAC CTG CCC TGC TGC GTG CCC GC - #G CGC CTG TCG CCC ATC1118Gly Ala Ala Asp Leu Pro Cys Cys Val Pro Al - #a Arg Leu Ser Pro Ile330 3 - #35 3 - #40 3 -#45- TCC GTG CTC TTC TTT GAC AAC AGC GAC AAC GT - #G GTG CTG CGG CAG TAT1166Ser Val Leu Phe Phe Asp Asn Ser Asp Asn Va - #l Val Leu Arg Gln Tyr# 360- GAG GAC ATG GTG GTG GAC GAG TGC GGC TGC CG - #C TAACCCGGGG CGGGCAGGGA1219Glu Asp Met Val Val Asp Glu Cys Gly Cys Ar - #g# 370# 1247 AATG CCGCGTGG- (2) INFORMATION FOR SEQ ID NO:33:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 372 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:33:- Met Pro Pro Pro Gln Gln Gly Pro Cys Gly Hi - #s His Leu Leu Leu Leu# 15- Leu Ala Leu Leu Leu Pro Ser Leu Pro Leu Th - #r Arg Ala Pro Val Pro# 30- Pro Gly Pro Ala Ala Ala Leu Leu Gln Ala Le - #u Gly Leu Arg Asp Glu# 45- Pro Gln Gly Ala Pro Arg Leu Arg Pro Val Pr - #o Pro Val Met Trp Arg# 60- Leu Phe Arg Arg Arg Asp Pro Gln Glu Thr Ar - #g Ser Gly Ser Arg Arg# 80- Thr Ser Pro Gly Val Thr Leu Gln Pro Cys Hi - #s Val Glu Glu Leu Gly# 95- Val Ala Gly Asn Ile Val Arg His Ile Pro As - #p Arg Gly Ala Pro Thr# 110- Arg Ala Ser Glu Pro Val Ser Ala Ala Gly Hi - #s Cys Pro Glu Trp Thr# 125- Val Val Phe Asp Leu Ser Ala Val Glu Pro Al - #a Glu Arg Pro Ser Arg# 140- Ala Arg Leu Glu Leu Arg Phe Ala Ala Ala Al - #a Ala Ala Ala Pro Glu145 1 - #50 1 - #55 1 -#60- Gly Gly Trp Glu Leu Ser Val Ala Gln Ala Gl - #y Gln Gly Ala Gly Ala# 175- Asp Pro Gly Pro Val Leu Leu Arg Gln Leu Va - #l Pro Ala Leu Gly Pro# 190- Pro Val Arg Ala Glu Leu Leu Gly Ala Ala Tr - #p Ala Arg Asn Ala Ser# 205- Trp Pro Arg Ser Leu Arg Leu Ala Leu Ala Le - #u Arg Pro Arg Ala Pro# 220- Ala Ala Cys Ala Arg Leu Ala Glu Ala Ser Le - #u Leu Leu Val Thr Leu225 2 - #30 2 - #35 2 -#40- Asp Pro Arg Leu Cys His Pro Leu Ala Arg Pr - #o Arg Arg Asp Ala Glu# 255- Pro Val Leu Gly Gly Gly Pro Gly Gly Ala Cy - #s Arg Ala Arg Arg Leu# 270- Tyr Val Ser Phe Arg Glu Val Gly Trp His Ar - #g Trp Val Ile Ala Pro# 285- Arg Gly Phe Leu Ala Asn Tyr Cys Gln Gly Gl - #n Cys Ala Leu Pro Val# 300- Ala Leu Ser Gly Ser Gly Gly Pro Pro Ala Le - #u Asn His Ala Val Leu305 3 - #10 3 - #15 3 -#20- Arg Ala Leu Met His Ala Ala Ala Pro Gly Al - #a Ala Asp Leu Pro Cys# 335- Cys Val Pro Ala Arg Leu Ser Pro Ile Ser Va - #l Leu Phe Phe Asp Asn# 350- Ser Asp Asn Val Val Leu Arg Gln Tyr Glu As - #p Met Val Val Asp Glu# 365- Cys Gly Cys Arg 370__________________________________________________________________________

Number	Name	Date
4806523	Bentz et al.	Feb 1989
4877864	Wang et al.	Oct 1989
4968590	Kuberasampath et al.	Nov 1990
4971952	Bentz et al.	Nov 1990
4975526	Kuberasampath et al.	Dec 1990
5002965	Ramwell et al.	Mar 1991
5011691	Oppermann et al.	Apr 1991
5013649	Wang et al.	May 1991
5091513	Huston et al.	Feb 1992
5106626	Parsons et al.	Apr 1992
5108753	Kuberasampath	Apr 1992
5118791	Burnier et al.	Jun 1992
5135915	Czarniecki et al.	Aug 1992
5141905	Rosen et al.	Aug 1992
5202311	Folkman et al.	Apr 1993
5221734	Burk et al.	Jun 1993
5972884	Cohen et al.	Oct 1999

Number	Date	Country
0148155	Jan 1985	EPX
0 269 408	Jun 1988	EPX
0416578	Sep 1990	EPX
WO9401106	Mar 1984	WOX
8800205	Jan 1988	WOX
8909788	Oct 1989	WOX
8909787	Oct 1989	WOX
8910409	Nov 1989	WOX
9000900	Feb 1990	WOX
9003733	Apr 1990	WOX
9105802	May 1991	WOX
9207073	Apr 1992	WOX
9215323	Sep 1992	WOX

	Number	Date	Country
Parent	165511	Dec 1993
Parent	938336	Aug 1992

	Number	Date	Country
Parent	753059	Aug 1991
Parent	667274	Aug 1991

Method for reducing tissue damage associated with ischemia-reperfusion or hypoxia injury

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CPC

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Abstract

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CROSS REFERENCE RELATIONSHIP TO RELATED APPLICATIONS

US Referenced Citations (17)

Foreign Referenced Citations (13)

Non-Patent Literature Citations (64)

Related Publications (1)

Continuations (2)

Continuation in Parts (2)

Entry
Behringer et al., Nature, 345:167-170 (1990).
Cate et al., Cell, 45:685-698 (1986).
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