Porcine E-selectin

Abstract

A porcine E-selectin protein, its amino acid sequence, the sequence of a cDNA encoding the protein, antibodies reactive with the protein, and methods for the use of these molecules are disclosed. The molecules are used to diagnose the rejection of xenotransplanted pig organs, as well as to prevent and treat such transplant rejection.

Description

FIELD OF THE INVENTION

This invention relates to xenotransplantation, and to the monitoring and modulation of the immune response to the xenotransplant. More specifically, the invention relates to the development of reagents and methods that will improve the ability to rapidly and specifically diagnose rejection of porcine xenotransplants by human patients. The invention also relates to compositions, including nucleic acid molecules, proteins (including antibodies), porcine cells, porcine tissues, and porcine organs, that will improve the outcome of the xenotransplantation of porcine cells, tissues, and organs into human recipients. To this end the invention provides a porcine E-selectin protein, its amino acid sequence, the sequence of a cDNA encoding the protein, antibodies reactive with the protein, and methods for the use of these molecules.

BACKGROUND OF THE INVENTION

Xenotransplant Rejection: There is an ongoing shortage of human organs for transplant. This shortage has resulted in a long felt need for organs, and has resulted in attempts to develop xenotransplantation technology.

The primary non-primate candidate donor species for clinical xenotransplantation (e.g., the transplantation of non-human organs into human recipients) has been the pig. Swine provide an abundant supply of organs that are similar in size, anatomy, and physiology to their human counterparts (Auchincloss, 1988; Najarian, 1992; and Somervile and d'Apice, 1993). Transplantation of porcine pancreatic islets and of a pig liver into human patients has been reported, (Makowka, et al., 1993; Satake, et al., 1993; Tibell, et al., 1993), but the outcomes of these transplants need to be improved. One improvement that is needed is better control (e.g., inhibition) of transplant rejection.

The rejection of transplanted organs may involve both an extremely rapid hyperacute rejection (HAR) phase and a slower cellular rejection phase. HAR of discordant (i.e., non-primate) xenotransplants is initiated by preformed "natural" antibodies that bind to donor organ endothelium and activate complement attack by the recipient immune system (Dalmasso, et al., 1992; and Tuso, et al., 1993).

Activation of complement leads to the generation of fluid phase (C3a, C5a) and membrane bound (C3b and C5b-9, i.e., C5b, C6, C7, C8, and C9) proteins with chemotactic, procoagulant, proinflammatory, adhesive, and cytolytic properties (Muler-Eberhard, 1988). Immunohistological analysis of hyperacutely rejected xenotransplants reveals antibody deposition, complement fixation, and vascular thrombosis as well as neutrophil infiltration (Zehr, et al., 1994; Auchincloss, 1988; Najarian, 1992; Somervile and d'Apice, 1993; and Mejia-Laguna, et al., 1972).

While HAR is a major impediment to the xenotransplantation of vascularized organs, some discordantly xenotransplanted tissues (e.g., porcine pancreatic islets) do not appear to be rejected by this mechanism. Methods for the control of the ITA are also available. These include interference with the antibody antigen reactions responsible for initiating the HAR response, either by removing the antibodies from the circulation or by interfering with the expression of the antigens (see U.S. Pat. No. 5,821,117, entitled "Xenotransplantation Therapies" and filed by Mauro S. Sandrin and Ian F. C. McKenzie on Mar. 15, 1994). Inhibition of complement attack on the xenotransplant may be accomplished by several means, including the use of complement inhibitors such as the 18kDa CSb-9 inhibitory protein and monoclonal antibodies against human C5b-9 proteins as taught in U.S. Pat. No. 5,135,916, issued Aug. 4, 1992.

In order to better understand the porcine xenograft rejection phenomenon, studies have been undertaken to investigate interactions between human white blood cells and porcine cells, particularly porcine aortic endothelial cells (PAEC). The role of neutrophils in the actual destruction of xenografts has not been well characterized, and the precise mechanism of complement independent neutrophil activation and adherence to xenograft endothelium has heretofore been unknown. Previous studies have shown that human complement component C3b (C3bi) deposited on PAEC mediates the binding of human neutrophils to the PAEC through interactions with the heterodimeric neutrophil cell surface receptor CD11b/CD18 (Vercellotti, et al., 1991). Furthermore, blocking HAR by inhibition or depletion of complement results in decreased neutrophil infiltration and increased xenograft survival, providing additional evidence for the role of complement in mediating human neutrophil binding to porcine endothelium.

However, a significant neutrophil infiltrate into PAEC monolayers has been observed even in the absence of complement activation (Leventhal, et al., 1993; and Pruitt, et al., 1991). The development of such infiltrates is believed to play an important role in xenograft rejection. Means and methods allowing the control or elimination of such interactions are thus needed in order to make the transplantation of porcine cells, tissues, or organs into human recipients more practicable.

E-selectin: E-selectin (also known as ELAM-1, CD62, and CD62E) is a cytokine inducible cell surface glycoprotein cell adhesion molecule that is found exclusively on endothelial cells. E-selectin mediates the adhesion of various leukocytes, including neutrophils, monocytes, eosinophils, natural killer (NK) cells and a subset of T cells, to activated endothelium (Bevilacqua, et al., 1989; Shimuzu, et al., 1991; Graber, et al., 1990; Carlos, et al., 1991; Hakkert, et al., 1991; and Picker, et al., 1991). The expression of E-selectin is induced on human endothelium in response to the cytokines IL-1 and TNF, as well as bacterial lipopolysaccharide (LPS), through transcriptional upregulation (Montgomery, et al., 1991).

Recently, the human leukocyte receptor for human E-selectin has been identified (Berg, et al., 1991 and Tyrrell, et al., 1991). This receptor contains sialic acid (sialyl Lewis x, and sialyl Lewis a) as a necessary component for interaction with the E-selectin protein.

Structurally, E-selectin belongs to a family of adhesion molecules termed "selections" that also includes P-selectin and L-selectin (see reviews in Lasky, 1992 and Bevilacqua and Nelson, 1993). These molecules are characterized by common structural features such as an amino-terminal lectin-like domain, an epidermal growth factor (EGF) domain, and a discrete number of complement repeat modules (approximately 60 amino acids each) similar to those found in certain complement binding proteins.

Clinically, increased E-selectin expression on endothelium is associated with a variety of acute and chronic leukocyte-mediated inflammatory reactions including allograft rejection (Allen, et al., 1993; Brockmeyer, et al., 1993; Ferran, et al., 1993; and Taylor, et al., 1992). Other leukocyte-mediated inflammatory reactions associated with increased E-selectin expression on endothelium include delayed type hypersensitivity, immune complex-mediated lung injury, psoriasis, contact dermatitis, inflammatory bowel disease, and arthritis (Bevilacqua, et al., 1989; Bevilacqua and Nelson, 1993; Cotran, et al., 1986; Koch, et al., 1991; Mulligan, et al., 1991; and Mulligan, et al., 1993).

Studies in which the expression of human E-selectin in cardiac and renal allografts undergoing acute cellular rejection was investigated have demonstrated that E-selectin expression is selectively upregulated in vascular endothelium of renal and cardiac tissue during acute rejection (Allen, et al., 1993; Brockmeyer, et al., 1993; Ferran, et al., 1993; and Taylor, et al., 1992). Additionally, increased E-selectin expression correlates with the early course of cellular rejection and corresponds to the migration of inflammatory cells into the graft tissue (Allen, et al., 1993; Brockmeyer, et al., 1993; Ferran, et al., 1993; and Taylor, et al., 1992). Taken together, these studies provide evidence that cytokine-induced expression of E-selectin by donor organ endothelium contributes to the binding and subsequent transmigration of inflammatory cells into the graft tissue and thereby plays an important role in acute cellular allograft rejection.

Endothelial cells have been shown to release a soluble form of E-selectin following in vitro activation (Pigott, et al., 1992; Newman, et al., 1993; and Leeuwenberg, et al., 1992). The demonstration of soluble E-selectin (sE-selectin) in the blood would therefore be taken as conclusive evidence of endothelial activation (Gearing and Newman, 1993). Table I shows the levels of sE-selectin found in healthy and sick patients in various studies, as reviewed in Gearing and Newman, 1993.

Elevated levels of sE-selectin have been found in diabetic patients independent of hypertension, nephropathy or renal failure, and whether or not they were insulin dependent (Gearing, et al., 1992 and Gearing and Newman, 1993). Similarly, sE-selectin was detected in patients with vasculidities including polyarteritis nodosum, giant cell arteritis, and scleroderma, with higher levels noted in lupus patients. Overall, however, there was no correlation with disease activity and only a weak correlation with the degree of organ involvement (Carson, et al., 1993). These studies suggest that the endothelium in these patients is activated, and that overt disease activity involves additional factors.

Soluble E-selectin levels have also shown marked elevations in sepsis, in one study a twenty-fold increase over the normal range (Newman, et al., 1993). In this and another study, the levels of sE-selectin appear to correlate with disease severity and/or outcome (Gearing and Newman, 1993). Higher levels or persistent elevation were associated with greater mortality and this is not unexpected in view of the widespread expression of E-selectin in most vessels in primates challenged with a lethal dose of live E. Coli (Redi, et al., 1991). Gram-negative as well as gram-positive infections seem to be associated with elevated levels. Patients with acute Plasmodium falciparum malaria have also shown elevated levels of sE-selectin (Hviid, et al., 1994, reviewed in Gearing and Newman, 1993).

There are two reports of sE-selectin in body fluids other than blood. One is from Dubois, et al., who detected sE-selectin in bronchioalveolar lavage (BAL) fluids from 16/50 patients with interstitial lung disease, but in only 2/16 control samples (Dubois, et al., unpublished, cited in Gearing and Newman, 1993). In the second, sE-selectin was recovered from BAL fluids of allergic subjects after segmental antigen challenge, but not saline challenge (Georas, et al., 1992).

Soluble E-selectin found in the blood is biologically active when measured by its ability to mediate adhesion of neutrophils to a surface. In the fluid-phase, recombinant soluble E-selectin can inhibit leukocyte adhesion (Lobb, et al., 1991). Furthermore, recombinant E-selectin, in either soluble or cell-surface bound forms, can activate the polymorphonuclear cell CD11b integrin receptor (Lo, et al., 1991 and Kuijpers, et al., 1991). The levels required for these effects are not found in the bloodstream, however such levels may be found at local sites of inflammation.

The mechanism of release of soluble E-selectin in vivo has not been established, but immunochemical evidence suggests a lost or defective cytoplasmic domain in the soluble E-selectin found in plasma. Unlike certain other cellular adhesion molecules, E-selectin does not appear to have an alternately spliced form lacking a transmembrane domain.

SUMMARY OF THE INVENTION

In view of the foregoing state of the art, it is an object of this invention to prevent and/or treat xenograft rejection of porcine organs, tissues, or cells through modulation of E-selectin mediated cell adhesion, and to provide a means for diagnostic monitoring of xenotransplant rejection by specific measurement of the amount of porcine E-selectin in the blood of the porcine xenotransplant recipient.

To achieve these and other goals, the invention provides:

1) An isolated porcine E-selectin protein including a core protein comprising the amino acid sequence set forth as amino acids 1 to 405 of SEQ ID NO:9. In addition to the core protein, such a porcine E-selectin protein may contain a membrane anchor sequence located carboxyl terminal to amino acid 405 of SEQ ID NO:9. Alternatively, the protein may be truncated. Examples of such truncated proteins include those that do not include the membrane anchor. For example, the protein may terminate at or near amino acid 405 of SEQ ID NO:9.

2) A porcine E-selectin gene, in the form of, for example, cDNA and genomic DNA molecules comprising porcine E-selectin coding sequences.

3) A method for producing porcine E-selectin by growing a recombinant host cell containing the gene of the invention (i.e., a nucleic acid molecule coding for porcine E-selectin). The host cell is grown so that it expresses the porcine E-selectin protein encoded by the gene of the invention and the expressed porcine E-selectin protein is then isolated.

4) Anti porcine E-selectin antibodies that bind to porcine E-selectin, but not to human E-selectin.

5) Therapeutic agents and methods for their use for the prevention and/or treatment of porcine xenograft rejection. These agents contain the E-selectin protein of paragraph 1, immediately above, and/or the anti-porcine E-selectin antibodies of paragraph 4, immediately above.

6) Agents for the diagnosis of porcine xenograft rejection based upon the anti-porcine E-selectin antibodies of paragraph 4, immediately above.

7) Methods for disrupting the porcine E-selectin gene in porcine cells, and the E-selectin negative porcine cells generated via such methods.

The accompanying drawings, which are incorporated in and constitute part of the specification, illustrate the preferred embodiments of the invention, and together with the description, serve to explain the principles of the invention. It is to be understood, of course, that both the drawings and the description are explanatory only and are not restrictive of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Amino acid comparison and domain structure comparison of porcine and human E-selectin: The porcine (PO) E-selectin amino acid sequence was aligned to the sequence and domain structure of human (HU) E-selectin. Identical amino acids are denoted by an asterisk (*) and gaps are denoted with horizontal lines (-). Domains are denoted by the following abbreviations: Signal peptide, SP; Lectin Domain, Lec; Epidermal growth factor domain, EGF; Complement repeats, CR1-CR6; Transmembrane domain, TM; Cytoplasmic tail, CYT. As noted below, the complement repeats #1 and #4 are absent from porcine E-selectin.

FIGS. 2A-2B. Human neutrophils and HL-60 cells bind to human cytokine-induced PAEC: The binding of calcein-labeled human neutrophils (FIG. 2A) and HL-60 cells (FIG. 2B) to confluent monolayers of cytokine-induced PAEC was determined. Neutrophils and HL-60 cells were incubated in a control buffer (solid bars), treated with neuraminidase (hatched bars) or incubated in the presence of 10 .mu.g/ml anti-LFA-1 (open bars) prior to addition to confluent monolayers of PAEC in 96 well plates. PAEC were incubated (37.degree. C., 4hr) in either medium containing 25 ng/ml human TNF.alpha. (TNF.alpha.), 20 ng/ml human IL-1 (IL-1), or media alone (UNINDUCED), prior to the addition of human neutrophils or HL-60 cells. Cell binding was determined as described below under the heading "Materials and Methods". Error bars denote standard error of triplicate determinations from a single experiment and are representative of three so performed.

FIG. 3. Binding of human neutrophils and HL-60 cells to COS cells transfected with porcine E-selectin: The binding of calcein-labeled human neutrophils and HL-60 cells to confluent monolayers of either vector control transfected (CONTROL) or porcine E-selectin transfected (PORCINE E-SELECTIN) COS cells was determined. Prior to addition to COS cells, human neutrophils or HL-60 cells were incubated in control buffer or treated with neuraminidase as indicated. Cell binding was determined as described below under the heading "Materials and Methods". Error bars denote standard errors from triplicate determinations from a single experiment and are representative of two so performed.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

As discussed above, the present invention relates to the cell adhesion protein, E-selectin, and specifically to the porcine E-selectin molecule. The data presented in the examples set forth below demonstrate that human white blood cells bind to porcine endothelial cells via binding to porcine E-selectin. This binding interaction has significant implications for the outcome of xenotransplantation of porcine organs into human recipients, as such binding of white blood cells to endothelial cells is one of the first steps in the pathway leading to cell-mediated rejection of transplanted endothelial cells, and of vascularized tissues and organs containing such cells.

The discovery of porcine nucleic acid sequences encoding porcine E-selectin provides means to reduce the binding of human white blood cells to porcine endothelial cells, as discussed below. Such inhibition will reduce the frequency with which such porcine endothelial cells, and vascularized tissues and organs containing such cells, are rejected following xenotransplantation into human recipients.

In accordance with the invention, as described in the examples presented below, it has been determined that porcine E-selectin is encoded by the coding region of the nucleic acid sequence of SEQ ID NO:1 and has the amino acid sequence set forth in SEQ ID NO:9. In accordance with certain of its aspects, the invention provides isolated nucleic acid molecules, membrane bound and soluble porcine E-selectin proteins and protein fragments, and antibodies related to porcine E-selectin.

The isolated nucleic acid molecules of the invention comprise sequences that are unique to the porcine genome. As used herein, the term "unique to the porcine genome" refers to sequences found in porcine-derived nucleic acid molecules that do not appear in published form as of the filing date of this application, e.g., they are not found in the cDNAs encoding the E-selectins of humans, cows, mice, or dogs.

The isolated nucleic acid molecules of the invention comprise sense sequences of contiguous nucleotides of SEQ ID NO:1. These sense sequences are unique to the porcine genome, and can be used as PCR primers or hybridization probes for the identification and/or isolation of the porcine E-selectin gene from genomic DNA. Antisense sequences of contiguous nucleotides complementary to such sense sequences are also required in order to practice PCR, and may also be used as hybridization probes. In order to be used for such purposes, the sequences of contiguous nucleotides must span a sufficient length. The minimum oligonucleotide length required for specific hybridization (i.e., hybridization under conditions requiring an essentially perfect match of complementary nucleotides wherein the sequence of the probe can be expected to occur only once in the genome of the organism being probed) of both hybridization probes and PCR primers is well known in the art, and is discussed in, for example, Sambrook, et al, 1989, on pages 11.7-11.8. In practice, this span is at least 14 nucleotides, and, preferably, at least 18 nucleotides. Because at least 2 PCR primers are generally required to carry out a PCR reaction, the specificity of the PCR reaction is greater than that of each of the oligonucleotide primers used to drive the reaction.

Another isolated nucleic acid molecule of the invention is a cloned porcine genomic DNA molecule comprising a sequence of nucleotides unique to the porcine genome. This cloned molecule is characterized by hybridizing specifically to an isolated nucleic acid molecule as described in the preceding paragraph. Specific hybridization is used to clone this genomic DNA molecule. This cloning can be accomplished by several methods well known in the art such as by PCR using porcine genomic DNA templates, or by conventional screening of phage libraries of porcine genomic DNA, e.g., by plaque lift filter hybridization.

The isolated nucleic acid molecules of the invention are also useful as means to direct and/or modulate the expression of porcine E-selectin in porcine cells, e.g., by altering the expression of the porcine E-selectin gene. Such modulation may be accomplished by several means well known in the art. Modulation, specifically inhibition, of the expression of any particular gene may be accomplished by the use of antisense nucleic acid molecules or DNA constructions specially engineered to allow gene inactivation as described below for antisense RNAs, antisense oligonucleotides, and gene knockout constructions. For the inhibition of the porcine E-selectin gene, the antisense nucleic acid molecules or DNA constructions will comprise nucleic acid sequences of the nucleic acid molecules of the invention.

Antisense RNAs can be used to specifically inhibit gene expression (see, for example, Eguchi, et al., 1991). Such nucleic acid molecules can be expressed by recombinant transcription units engineered for expression in porcine cells. Such transcription units can be introduced as transgenes into porcine cells, and, when introduced into porcine embryos or embryonic stem cells can be used to generate transgenic pigs.

Antisense nucleic acid molecules in the form of oligonucleotides (including oligonuclotide analogs) and derivatives thereof can also be used to specifically inhibit gene expression, as described, for example, in Cohen, 1989. As described therein, antisense oligonucleotides can be designed and used to inhibit expression of specific genes (Cohen, 1989, pp. 1-6, 53-77).

Such antisense oligonucleotides can be in the form of oligonucleotide analogs, for example, phosphorothioate analogs (Cohen, 1989, pp. 97-117), non-ionic analogs (Cohen, 1989, pp. 79-95), and .alpha.-oligodeoxynucleotide analogs (Cohen, 1989, pp. 119-136). Derivatives of oligonucleotides that can be used to inhibit gene expression include oligonucleotides covalently linked to intercalating agents or to nucleic acid-cleaving agents (Cohen, 1989, pp. 137-172), and oligonucleotides linked to reactive groups (Cohen, 1989, pp. 173-196). oligonucleotides and derivatives designed to recognize double-helical DNA by triple-helix formation (Cohen, 1989, pp. 197-210) may also be used to specifically inhibit gene expression.

All of the oligonucleotides and derivatives described above are used by adding them to the fluids bathing the cells in which specific inhibition of gene expression in accordance with the present invention is desired.

Another method by which the expression of specific genes can be inhibited is by genetic manipulations referred to in the art as "gene disruption" or "gene knockout." Gene knockout is a method of genetic manipulation via homologous recombination that has long been carried out in microorganisms, but has only been practiced in mammalian cells within the past decade. These techniques allow for the use of specially designed DNA molecules (gene knockout constructions) to achieve targeted inactivation (knockout) of a particular gene upon introduction of the construction into a cell. The practice of mammalian gene knockout, including the design of gene knockout constructions and the detection and selection of successfully altered mammalian cells, is discussed in numerous publications, including Thomas, et al., 1986; Thomas, et al., 1987; Jasin and Berg, 1988; Mansour, et al., 1988; Brinster, et al., 1989; Capecchi, 1989; Frohman and Martin, 1989; Hasty, et al., 1991; Jeannotte, et al., 1991; and Mortensen, et al., 1992.

Gene knockouts and gene replacements can be achieved in mammalian zygotes through microinjection techniques well known in the art (Brinster, et al., 1989). The introduction of the DNA constructions used to effect gene knockouts into cultured cells is a more common route to the production of knockout cells, tissues, and organs. In those cases where knockout tissues or organs are desired, cultured embryonic stem cells provide a means to introduce the DNA constructions into cells in culture and to generate transgenic animals derived from such engineered cells. Such animals can also be obtained from knockout transgenic zygotes obtained by microinjection as described above.

Thus, in accordance with certain aspects of the invention, the nucleic acid molecules of the present invention are used to generate engineered transgenic animals using techniques known in the art. These techniques include, but are not limited to, microinjection, e.g., of pronuclei, electroporation of ova or zygotes, nuclear transplantation, and/or the stable transfection or transduction of embryonic stem cells.

The most well known method for making transgenic animals is that used to produce transgenic mice by superovulation of a donor female, surgical removal of the egg, injection of the transgene transcription unit into the pro-nuclei of the embryo, and introduction of the transgenic embryo into the reproductive tract of a pseudopregnant host mother, usually of the same species. See Wagner, U.S. Pat. No. 4,873,191, Brinster, et al., 1985, Hogan, et al., 1986, Robertson 1987, Pedersen, et al., 1990.

The use of this method to make transgenic livestock is also widely practiced by those of skill in the art. As an example, transgenic swine are routinely produced by the microinjection of nucleic acid molecules into pig embryos. See, for example, PCT Publication No. WO92/11757. In brief, this procedure may, for example, be performed as follows. First, the nucleic acid molecules are gel isolated and extensively purified, for example, through an ELUTIP column (Schleicher & Schuell, Keene, N. H.), dialyzed against pyrogen free injection buffer (10 mM Tris, pH7.4+0.1 mM EDTA in pyrogen free water), and used for embryo injection.

Embryos are recovered from the oviduct of a hormonally synchronized, ovulation induced sow, preferably at the pronuclear stage. They are placed into a 1.5 ml microfuge tube containing approximately 0.5 ml of embryo transfer media (phosphate buffered saline with 10% fetal calf serum). These are centrifuged for 12 minutes at 16,000.times. g in a microcentrifuge. Embryos are removed from the microfuge tube with a drawn and polished Pasteur pipette and placed into a 35 mm petri dish for examination. If the cytoplasm is still opaque with lipid such that the pronuclei are not clearly visible, the embryos are centrifuged again for an additional 15 minutes.

Embryos to be microinjected are placed into a drop of media (approximately 100 .mu.l) in the center of the lid of a 100 mm petri dish. Silicone oil is used to cover this drop and to fill the lid to prevent the medium from evaporating. The petri dish lid containing the embryos is set onto an inverted microscope equipped with both a heated stage (37.5-38.degree. C.) and Hoffman modulation contrast optics (200X final magnification). A finely drawn and polished micropipette is used to stabilize the embryos while about 1-2 picoliters of injection buffer containing approximately 200-500 copies of the purified transgene transcription unit is delivered into the nucleus, preferably the male pronucleus, with another finely drawn and polished micropipette. Embryos surviving the microinjection process as judged by morphological observation are loaded into a polypropylene tube (2 mm ID) for transfer into the recipient pseudopregnant sow.

Offspring are tested for the presence of the transgene by isolating genomic DNA, e.g., from tissue removed from the tail of each piglet, and subjecting about micrograms of this genomic DNA to nucleic acid hybridization analysis with a transgene specific probe.

Another commonly used technique for generating transgenic animals involves the genetic manipulation of embryonic stem cells (ES cells) as described in PCT Patent Publication No. WO 93/02188 and Robertson, 1987. In accordance with this technique, ES cells are grown as described in, for example, Robertson, 1987, and in U.S. Pat. No. 5,166,065 to Williams et al. Genetic material is introduced into the embryonic stem cells by, for example, electroporation according, for example, to the method of McMahon, et al., 1990, or by transduction with a retroviral vector according, for example, to the method of Robertson, et al., 1986, or by any of the various techniques described by Lovell-Badge, 1987.

Chimeric animals are generated as described, for example, in Bradley, 1987. Briefly, genetically modified ES cells are introduced into blastocysts and the modified blastocysts are then implanted in pseudo-pregnant female animals. Chimeras are selected from the offspring, for example by the observation of mosaic coat coloration resulting from differences in the strain used to prepare the ES cells and the strain used to prepare the blastocysts, and are bred to produce non-chimeric transgenic animals.

Other methods for the production of transgenic animals are disclosed in U.S. Pat. No. 5,032,407 to Wagner et al., and PCT Publication No. WO90/08832.

The practice of gene knockout in embryonic stem cells, and the generation of engineered animals from such cells, is discussed in numerous publications, including Thomas, et al., 1987; Robertson, 1987; Mansour, et al., 1988; Capecchi, 1989; Frohman and Martin, 1989; Hasty, et al., 1991; Jeannotte, et al., 1991; Mortensen, et al., 1992; Thomas, et al., 1992; and PCT Patent Publication No. WO 93/02188.

Among other applications, transgenic pigs prepared in accordance with the invention are useful as model systems for testing the xenotransplantation of their engineered cells, tissues, or organs and as sources of engineered cells, tissues, or organs for xenotransplantation. The lack of expression of porcine E-selectin on the endothelial cells of the transgenic pigs will provide enhanced protection from rejection following xenotransplantation of those cells, or of tissues and organs containing those cells, into recipient animals, e.g., humans. In addition to their use in producing tissues, and organs for transplantation, the nucleic acid molecules of the invention can also be used to directly engineer cultured porcine endothelial cells for subsequent use in transplantation.

The nucleic acid molecules of the invention can also be used to express porcine E-selectin proteins for subsequent purification and use. Recombinant DNA methods for the production of recombinant proteins are well known in the art, as are methods for the purification of such proteins (see, for example, Ausubel, et al., 1992; Goeddel, 1990; Harris and Angal, 1989; and Deutscher, 1990). The production of soluble porcine E-selectin by such means is described below under the heading "Materials and Methods, and under the subheadings "generation of vectors directing the expression of soluble porcine E-selectin", "generation of stabily transfected cells secreting porcine E-selectin", and "purification and characterization of soluble porcine E-selectin protein", and is also described below in Example 6. Preferred uses of such proteins include the use of soluble porcine E-selectin as an immunogen for the purpose of raising anti porcine E-selectin antibodies, or as an antigen for use in an immunoassay as described below under the heading "Materials and Methods", and under the subheading "ELISA screen for anti-porcine E-selectin antibodies".

The present invention provides recombinant expression vectors which include synthetic or cDNA-derived DNA fragments encoding porcine E-selectin. The nucleotide sequence coding for porcine E-selectin can be inserted into an appropriate expression vector, i.e., a vector that contains the necessary elements for the transcription and translation of the inserted protein-coding sequence. The necessary transcriptional and translational signals can also be supplied by the native gene and/or its flanking regions. A variety of host vector systems may be utilized to express the protein-coding sequence. These include, but are not limited to, mammalian cell systems infected with virus (e.g., vaccinia virus, adenovirus, retroviruses, etc.); mammalian cell systems transfected with plasmids; insect cell systems infected with virus (e.g., baculovirus); microorganisms such as yeast containing yeast expression vectors, or bacteria transformed with bacteriophage DNA, plasmid DNA, or cosmid DNA (see, for example, Goeddel, 1990).

Useful expression vectors for bacterial use can comprise a selectable marker and bacterial origin of replication derived from commercially available plasmids comprising genetic elements of the well-known cloning vector pBR322 (American Type Culture Collection, 12301 Parklawn Drive, Rockville, Md. 20852, United States of America; ATCC Accession No. 37017). These pBR322 "backbone sections," or functionally equivalent sequences, are combined with an appropriate promoter and the structural gene to be expressed. Promoters commonly used in recombinant microbial expression vectors include, but are not limited to, the lactose promoter system (Chang, et al., 1978), the tryptophan (trp) promoter (Goeddel, et al., 1980) and the tac promoter, or a fusion between the tac and trp promoters referred to as the trc promoter (Maniatis, 1982). Preferred bacterial expression vectors include, but are not limited to, vector pSE420 (Invitrogen Corporation, San Diego, Calif.). This vector harbors the trc promoter, the lacO operon, an anti-terminator sequence, the g10 ribosome binding sequence, a translation terminator sequence, the lacIq repressor, the ColE1 origin of replication, and the ampicillin resistance gene.

Recombinant porcine E-selectin may also be expressed in fungal hosts, preferably yeast of the Saccharomyces genus such as S. cerevisiae. Fungi of other genera such as Aspergillus, Pichia or Kluyveromyces may also be employed. Fungal vectors will generally contain an origin of replication from the 2 .mu.m yeast plasmid or another autonomously replicating sequence (ARS), a promoter, DNA encoding porcine E-selectin, sequences directing polyadenylation and transcription termination, and a selectable marker gene. Preferably, fungal vectors will include an origin of replication and selectable markers permitting transformation of both E. coli and fungi.

Suitable promoter systems in fungi include the promoters for metallothionein, 3-phosphoglycerate kinase, or other glycolytic enzymes such as enolase, hexokinase, pyruvate kinase, glucokinase, the glucose-repressible alcohol dehydrogenase promoter (ADH2), the constitutive promoter from the alcohol dehydrogenase gene, ADH1, and others. See, for example, Schena, et al. 1991. Secretion signals, such as those directing the secretion of yeast a-factor or yeast invertase, can be incorporated into the fungal vector to promote secretion of a soluble porcine E-selectin into the fungal growth medium. See Moir, et al., 1991.

Preferred fungal expression vectors can be assembled using DNA sequences from pBR322 for selection and replication in bacteria, and fungal DNA sequences, including the ADH1 promoter and the alcohol dehydrogenase ADH1 termination sequence, as found in vector PAAH5 (Ammerer, 1983). The ADH1 promoter is effective in yeast in that ADH1 mRNA is estimated to be 1-2% of total poly(A) RNA.

Various mammalian or insect cell culture systems can be employed to express recombinant porcine E-selectin. Suitable baculovirus systems for production of heterologous proteins in insect cells are reviewed by Luckow, et al., 1988. Examples of suitable mammalian host cell lines include the COS cell of monkey kidney origin, mouse L cells, murine C127 mammary epithelial cells, mouse Balb/3T3 cells, Chinese hamster ovary cells (CHO), human 293 EBNA and HeLa cells, myeloma, and baby hamster kidney (BHK) cells. Mammalian expression vectors may comprise non-transcribed elements such as origin of replication, a suitable promoter and enhancer linked to the porcine E-selectin gene to be expressed, and other 5' or 3' flanking sequences such as ribosome binding sites, a polyadenylation sequence, splice donor and acceptor sites, and transcriptional termination sequences.

The transcriptional and translational control sequences in mammalian expression vector systems to be used in transforming vertebrate cells may be provided by viral sources. For example, commonly used promoters and enhancers are derived from Polyoma virus, Adenovirus, Simian Virus 40 (SV40), and human cytomegalovirus, including the cytomegalovirus immediate-early gene 1 promoter and enhancer (CMV).

Particularly preferred eukaryotic vectors for the expression of porcine E-selectin are pAPEX-1 and pAPEX-3, as described below under the heading "Materials and Methods," and under the subheadings "assays for binding of human neutrophils and HL-60 cells to porcine E-selectin transfected COS cells," and "generation of vectors directing the expression of soluble porcine E-selectin". A particularly preferred host cell for the expression of inserts in the pAPEX-3 vector is the human 293 EBNA cell line (Invitrogen, San Diego, Calif.).

Another preferred eukaryotic vector for the expression of porcine E-selectin is pcDNAI/Amp (Invitrogen Corporation, San Diego, Calif.). The pcDNAI/Amp expression vector contains the human cytomegalovirus immediate-early gene I promoter and enhancer elements, the Simian Virus 40 (SV40) consensus intron donor and acceptor splice sequences, and the SV40 consensus polyadeaylation signal. This vector also contains an SV40 origin of replication that allows for episomal amplification in cells (e.g., COS cells, MOP8 cells, etc.) transformed with SV40 large T antigen, and an ampicillin resistance gene for propagation and selection in bacterial hosts.

Purified porcine E-selectin is prepared by culturing suitable host/vector systems to express the recombinant translation products of the nucleic acid molecules of the present invention, which are then purified from the culture media or cell extracts of the host system, e.g., the bacteria, insect cells, fungal, or mammalian cells. Fermentation of fungi or mammalian cells that express soluble porcine E-selectin protein containing a histidine tag sequence (comprising a string of at least 5 histidine residues in a row) as a secreted product greatly simplifies purification. Such a histidine tag sequence enables binding under specific conditions to metals s, as nickel, and thereby to nickel columns for purification. Specific examples of the generation of a porcine E-selectin protein containing such a histidine tag sequence and its purification is set forth below under the head "Materials and Methods", and under the subheadings "generation of vectors directing the expression of soluble porcine E-selectin", and "purification and characterization of soluble porcine E-selectin protein".

In general terms, the purification of recombinant porcine E-selectin is performed using a suitable set of concentration, fractionation, and chromatography steps well known in the art (see, for example, Deutscher, 1990; and Harris and Angal, 1989). For recombinant porcine E-selectins requiring correct disulfide bond formation for full biological activity, denaturation of the purified protein followed by chemical-mediated refolding under reducing conditions can be done to promote proper disulfide interactions.

Porcine E-selectin proteins purified from bodily fluids of transgenic animals engineered to produce the porcine E-selectins of the invention are also with the scope of the invention, as are porcine E-selectins that are produced in part or entirely by chemical synthesis.

Porcine E-selectins synthesized in recombinant culture and subsequently purified may be characterized by the presence of contaminating components. These components may include proteins or other molecules in amounts and of a character which depend on the production and purification processes. These components will ordinarily be of viral, prokaryotic, eukaryotic, or synthetic origin, and preferably are present in innocuous contaminant quantities, on the order of less that about 1% by weight. Recombinant cell culture, however, enables the production of porcine E-selectins relatively free of other proteins that may normally be associated with the protein as it is found in nature.

As discussed above, certain aspects of the present invention relates to the use of anti porcine E-selectin antibodies or soluble E-selectin protein (collectively referred to hereinafter as therapeutic E-selection agents") in treating patients suffering from xenotransplant rejection. The therapeutic E-selectin agents are used in an amount effective to achieve blood concentrations equivalent to in vitro concentrations that substantially reduce (e.g., reduce by at least about 50% the binding of human test cells expressing the human E-selectin binding ligand, such as PBLs, neutrophils, and HL-60 cells, to cells expressing porcine E-selectin, such as TNF.alpha. treated porcine endothelial cells. Reduction of the binding of human test cells to cells expressing porcine E-selectin can be measured by methods well known in the art such as, for example, by the assay described below under the heading "assays for neutrophil/HL-60 binding to PAEC".

To achieve the desired reductions in binding, the therapeutic E-selectin agents can be administered in a variety of unit dosage forms. The dose will vary according to the particular agent. For example, different antibodies may have different masses and/or affinities, and thus require different dosage levels. Antibodies prepared as Fab' or F(ab').sub.2 fragments will also require differing dosages than the equivalent intact immunoglobulins, as they are of considerably smaller mass than intact immunoglobulins, and thus require lower dosages to reach the same molar levels in the patient's blood.

The dose will also vary depending on the manner of administration, the particular symptoms of the patient being treated, the overall health, condition, size, and age of the patient, and the judgment of the prescribing physician. Dosage levels of the therapeutic E-selectin agents for human subjects are generally between about 1 mg per kg and about 100 mg per kg per patient per treatment, and preferably between about 5 mg per kg and about 50 mg per kg per patient per treatment. In terms of plasma concentrations, the therapeutic E-selectin agent concentrations are preferably in the range from about 25 .mu.g/ml to about 500 .mu.g/ml.

Subject to the judgement of the physician, a typical therapeutic treatment includes a series of doses, which will usually be administered concurrently with the monitoring of clinical endpoints such as xenotransplant biopsies, or measures of organ function, such as, for example, for xenotransplanted kidneys, BUN levels proteinuria levels, etc., with the dosage levels adjusted as needed to achieve the desired clinical outcome.

The therapeutic E-selectin agents of the present invention can be used in therapeutic compositions to treat episodes of xenograft rejection. Such treatment will result in the reduction of the severity of the rejection episode. For such application, purified therapeutic E-selectin agents can be administered to a patient, e.g., human, in a variety of ways. Thus, therapeutic E-selectin agents can be given by bolus injection, continuous infusion, sustained release from implants, or other suitable techniques.

Formulations suitable for injection are found Remington's Pharmaceutical Sciences, Mack Publishing Company, Philadelphia, Pa., 17th ed. (1985). Such formulations must be sterile and non-pyrogenric, and generally will include purified therapeutic E-selectin agents in conjunction with a pharmaceutically effective carrier, such as saline, buffered (e.g., phosphate buffered) saline, Hank's solution, Ringer's solution, dextrose/saline, glucose solutions, and the like. The formulations may contain pharmaceutically acceptable auxiliary substances as required, such as, tonicity adjusting agents, wetting agents, bactericidal agents, preservatives, stabilizers, and the like.

In one preferred embodiment, the therapeutic E-selectin agent is formulated as a lyophilizate using appropriate excipient solutions (e.g., sucrose, albumin) as diluents. The amount and frequency of administration will depend, of course, on such factors as the nature and severity of the rejection episode being treated, the desired response, the condition of the patient, and so forth.

The formulations of the invention can be distributed as articles of manufacture comprising packaging material and the therapeutic E-selectin agents. The packaging material will include a label which indicates that the formulation is for use in the treatment of porcine xenotransplant rejection.

Hybridomas producing the monoclonal antibodies of the invention, i.e., monoclonal antibodies reactive with porcine E-selectin, but not with human E-selectin, can be obtained using purified porcine E-selectin as an immunogen followed by screening. Such screening is carried out to identify hybridomas producing antibodies with the desired properties, and can be carried out using appropriate immunoassays. Examples of appropriate immunoassays are the ELISA described below under the heading "Materials and Methods, and under the subheading "ELISA screen for anti-porcine E-selectin antibodies". This ELISA can be used to identify hybridomas producing antibodies that bind to porcine E-selectin. A simple modification of this ELISA (consisting of substituting soluble human E-selectin for soluble porcine E-selectin) can be used to identify those of the hybridomas producing antibodies that bind to porcine E-selectin in which the antibodies do not bind to human E-selectin.

General methods for the immunization of animals this case with porcine E-selectin), isolation of antibody producing cells, fusion of such cells with immortal cells (e.g., myeloma cells) to generate hybridomas secreting monoclonal antibodies, screening of hybridoma supernatants for reactivity and/or lack of reactivity of secreted monoclonal antibodies with particular antigens (in this case reactivity with porcine E-selectin but not with human E-selectin), the preparation of quantities of such antibodies in hybridoma supernatants or ascites fluids, and for the purification and storage of such monoclonal antibodies, can be found in numerous publications. These include: Coligan, et al., eds. Current Protocols In Immunology, John Wiley & Sons, New York, 1992; Harlow and Lane, Antibodies. A Laboratory Manual, Cold Spring Harbor Laboratory, New York, 1988; Liddell and Cryer, A Practical Guide To Monoclonal Antibodies, John Wiley & Sons, Chichester, West Sussex, England, 1991; Montz, et al., 1990; Wurzner, et al., 1991; and Mollnes, et al., 1988.

The present invention also includes porcine E-selectins and anti porcine E-selectin antibodies with or without associated native patterns of glycosylation. For example, expressing proteins recombinantly in bacteria such as E coli provides non-glycosylated molecules, while expressing porcine E-selectins or anti porcine E-selection antibodies in mammalian cells can provide glycosylated molecules.

As used herein, the term "antibodies" refers to immunoglobulins produced in vivo, as well as those produced in vitro by a hybridoma, and antigen binding fragments (e.g., Fab' preparations) of such immunoglobulins, as well as to recombinantly expressed antigen binding proteins, including immunoglobulins, chimeric immunoglobulins, "humanized" immunoglobulins, antigen binding fragments of such immunoglobulins, single chain antibodies, and other recombinant proteins containing antigen binding domains derived from immunoglobulins. Publications describing methods for the preparation of such antibodies, in addition to those listed immediately above, include: Reichmann, et al., 1988; Winter and Milstein, 1991; Clackson, et al., 1991; Morrison, 1992; Haber, 1992; and Rodrigues, et al., 1993.

Diagnostic use of the anti porcine E-selectin antibodies of the invention can be carried out by assaying the patient's blood for levels of porcine E-selectin. Assays for porcine E-selectin levels may be by RIA, ELISA or other suitable immunoassay using the anti porcine E-selectin antibodies of the invention. General methods for performing such assays are set forth in Coligan, et al., 1992. Blood porcine E-selectin levels must be monitored at regular intervals, e.g., daily or weekly, and changes in such levels recorded. Any distinct increase in porcine E-selectin levels in the patient's blood is an indication that the porcine endothelium is being activated, and may indicate the onset of a rejection episode.

An alternative test for rejection, (or a test providing confirmation of the occurrence of rejection as indicated by measurement of soluble E-selectin levels) may be obtained by monitoring porcine organ function or by biopsy and histopathological examination of the porcine organ. Such examination will be carried out in order detect the typical manifestations of transplant rejection e.g., cellular infiltrates, inflammation, and necrosis. In accordance with the invention, the histopathological examination of xenotransplanted organ biopsy tissues will also include the use of the antibodies of the invention to detect the levels of expression of porcine E-selectin on the surfaces of the cells of the biopsied tissues of xenotransplanted organ. High levels of such express (compared to levels on non-transplanted control tissue samples) are indicative of xenotransplant rejection.

Although specific embodiments of the invention described and illustrated herein, it is to be understood that modifications can be made without departing from the invention's spirit and scope.

For example, the nucleotide sequences of the porcine E-selectin-encoding nucleic acid molecules of the invention may be modified by creating nucleic acid mutations which do not significantly change the encoded amino acid sequences. Such mutations include third nucleotide changes in degenerate codons (and other "silent" mutations that do not change the encoded amino acid sequence).

Other such mutations within the scope of invention and considered as equivalents of the specific embodiments set forth herein include those which result in a highly conservative amino acid substitution for an encoded amino acid while leaving the leucocyte binding characteristics of the porcine E-selectin molecule essentially unchanged. Such silent or highly conservative mutations are included within the scope of the invention.

Also included are:

1) Nucleotide and amino acid sequences comprising changes that are found as naturally occurring allelic variants of the porcine E-selectin gene; 2) Sequences which have been truncated so as to only encode the mature porcine E-selectin polypeptide, i.e., a porcine E-selectin polypeptide without the amino terminal leader sequence that directs the protein to its typical transmembrane orientation in the cell, indicated by negative amino acid numbers in SEQ ID NO:9; 3) Sequences in which the E-selectin amino terminal leader sequence has been altered, e.g., substituted with a different leader; 4) Sequences in which a peptide "tag" sequence has been inserted or added on to enable the ready identification and/or purification of recombinant proteins. Such tags include the FLAG epitope (which enables specific binding to anti-FLAG antibodies) and a histidine tag sequence, as described above; 5) Sequences that have been altered to produce a soluble porcine E-selectin protein by, for example, truncation near amino acid number 405 of SEQ ID NO:9 as described below under the heading "Materials and Method" and the sub-heading "generation of vectors directing the expression of soluble porcine E-selectin." Such soluble selectin proteins and sequence alterations have also been described for the human E-selectin molecule. The generation of recombinant soluble human E-selectin molecules is disclosed in Lobb, et al., 1991, and PCT patent publication No. WO 93/07268.

Without intending to limit it in any manner, the present invention will be more fully described by the following examples. Materials and methods used in various of the examples are as follows.

MATERIALS AND METHODS

Materials: A monoclonal antibody to human LFA-1 (clone 25.3) was obtained from AMAC Inc, Westbrook Minn. Human TNF.alpha. and IL-1 were obtained from Collaborative Biomedical Products, Bedford Mass. Dulbecco's modified Eagles medium (DMEM) and RPMI-1640 medium were purchased from JRH Biosciences, Lenexa Kans. Fetal bovine serum (FBS) was purchased from Harlan, Indianapolis Ind. Sterilie Hank's balanced salt solution (HBSS) and phosphate buffer saline (PBS) were purchased from Bio Whittaker, Walkersville Md. Calcein AM was obtained from Molecular Probes, Eugene Oreg. Neuraminidase was purchased from Boehringer Mannheim, Indianapolis Ind. All other reagents were of analytical grade or better and purchased from Sigma Chemical Co., Saint Louis Mo., unless otherwise specified.

Cell culture: Porcine aortic endothelial cells (PAED were obtained at passage 1 (Cell Systems, Kirkland Wash.) a maintained in DMEM containing 10% FBS, penicillin 100 U/ml, and streptomycin 100 .mu.g/ml (pen/strep, JRH Biosciences, Lenexa KS), hereinafter referred to as D10 medium. PAEC were at passage 2-4 in all assays. For cell binding assays, PAEC were removed from culture flasks with trypsin EDTA and replated onto 96 well culture dishes at a density of 1.times.10.sup.4 cells/well. The human promyelocytic leukemia cell line HL-60 was obtained from the American Type Culture Collection (ATCC), Rockville, Md. and maintained in D10.

Assays for Neutrophil/HL-60 binding to PAEC: Confluent monolayers of PAEC in 96 well plates were incubated (4 hr, 37.degree. C.) in 200 .mu.l/well DMEM alone, DMEM containing 25 ng/ml human TNF.alpha., or DMEM containing 10 ng/ml human IL-1. During this incubation, human neutrophils were isolated from 60 ml of human blood obtained from a healthy donor using the manufacturer's protocol (Polymorphoprep, Oslo, Norway), or HL-60 cells were spun down from culture medium.

The isolated neutrophils or HL-60 cells were washed 2.times. with HBSS, resuspended in HBSS containing 1% BSA (HBSS/BSA) at a final concentration of 3.times.10.sup.6 cells/ml, incubated (30 min, 37.degree. C.) in the cytoplasmic indicator calcein AM (10 .mu.M), washed 2.times. with HBSS and resuspended 3.times.10.sup.6 cells/ml in HBSS/BSA. Prior to addition to PAEC monolayers, the purified human neutrophils or HL-60 cells were incubated (30 min, 37.degree. C.) in either, HBSS/BSA, HBSS/BSA containing 0.25 U/ml neuraminidase, or HBSS/BSA containing 10 .mu.g/ml anti-LFA-1 mAb.

Following this incubation, the neutrophils or HL-60 cells were washed 2.times. with HBSS/BSA and resuspended to 3 .times.10.sup.6 cells/ml. PAEC monolayers were then washed 3.times. with HBSS/BSA and calcein-loaded human neutrophils or HL-60 cells were added at 3.times.10.sup.5 cells/well. The plates were centrifuged briefly (250.times. g, 1 minute), incubated in the dark for 5 min at 37.degree. C. and then centrifuged upside down 250.times. g for 3 minutes. The media and unbound neutrophils or HL-60 cells were removed from the plate and the bound cells were lysed by the addition of 1% SDS (100 .mu.l/well) in HBSS. Neutrophil or HL-60 cell binding was determined by measuring the release of calcein from bound neutrophils or HL-60 cells into the lysis buffer using a Cytofluor 2350 (Millipore, Bedford Mass.--excitation wavelength=485 nm, emission wavelength=530 nm). Background fluorescence was determined from wells containing PAEC that did not receive labeled neutrophils or HL-60 cells. Cloning and Sequencing: PAEC were grown to near confluence and stimulated with human TNF.alpha. (20 nag/ml) in D10 for 4 hours at 37.degree. C. Total RNA was isolated from these cells using the acid/guanidinium thiocyanate technique (Chomczynski and Sacchi, 1987). Ten micrograms of total RNA was heated at 65.degree. C. for 3 min and quenched on ice before first strand cDNA synthesis was carried out for 1 hr at 37.degree. C. in the following reaction mixture: 10 mM Tris-HCl (pH 8.3), 50 mM KCl, 1.5 mM MgCl.sub.2, 10 mM dithiothreotol, 0.25 mM of each dNTP, 0.5 .mu.g oligo dT.sub.16, and 20 U of avian myeloblastosis virus reverse transcriptase (Seikagaku Inc, Rockville Md.).

The cDNA pool (5 .mu.l of first strand cDNA reaction mixture) was used as a template in a 100 .mu.l PCR reaction under the following reaction conditions: 50 mM KCl, 10 mM Tris-HCL (pH 9.0), 1.5 mM MgCl.sub.2, 0.1% (w/v) gelatin, 1% Triton X-100, 200 .mu.M each dNTP, 2.5 U Taq DNA polymerase (Perkin Elmer Cetus, Norwalk Conn.) using 25 pmol of each primer--oligo 138 (SEQ ID NO:2) and oligo 139 (SEQ ID NO:3). PCR amplification was performed for 40 cycles (95.degree. C. for 1 min, 42.degree. C. for 2 min, 72.degree. C. for 2 min) followed by 1 cycle at 72.degree. C. for 10 min.

The resulting approximately 150 base pair PCR fragment (referred to hereinafter as the "150 bp fragment") was cloned into the pCRII vector using the T/A cloning system (which includes the PCRII vector) as described by the manufacturer (Invitrogen, San Diego Calif.). The 150 bp fragment in pCRII was subjected to sequence analysis (Sanger, et al., 1977). Comparison of the non-oligonuclotide derived sequence of this PCR fragment (nucleotide 357 through nucleotide 454 of SEQ ID NO:1) with those of human and mouse E-selectin confirmed that the fragment encoded an amino acid sequence that was homologous to the lectin binding domains of the human and mouse proteins.

The 150 base pair fragment was subsequently used to screen a UNI-ZAP XR cDNA library (Stratagene, La Jolla Calif.) constructed from PAEC RNA prepared following stimulation of PAEC with human TNF.alpha. as described above. The library was plated and screened as recommended by the supplier's protocol with only minor modifications.

Briefly, 1.times.10.sup.6 phage were isolated on nitrocellulose lifts which were subsequently denatured, neutralized, and air dried. Denatured filters were prehybridized in BSA/SDS buffer (Church and Gilbert, 1984) for 2 hr at 60.degree. C. before addition of the 150 base pair fragment which had been .sup.32 P labeled with the PRIME IT random primer kit (Stratagene, La Jolla Calif.) to a specific activity of 1.times.10.sup.9 CPM/.mu.g of DNA. Membranes were hybridized at 60.degree. C. overnight and subsequently washed using the following conditions: two-30 min washes with 2.times. SSC/0.1% SDS at room temperature followed by two-30 min washes with 0.5.times. SSC/0.1% SDS at 60.degree. C.

Positive plaques present on duplicate lifts, were purified and plasmid (BLUESCRIPT SK.sup.- phagemid) DNA rescued in accordance with the instructions of the UNI-ZAP XR vector manufacturer (Stratagene, La Jolla Calif). Both strands of a putative full-length clone of approximately 3.4 kb (designated "porcine E-selectin/pBLUESCRIPT SK.sup.- " were sequenced through the coding region using the chain termination method (Sanger, et al., 1977). The DNA template was primed with vector primers flanking the multiple cloning site of the BLUESCRIPT SK.sup.- vector or primers constructed subsequent to the initial sequencing runs from the internal cDNA sequence. The sequence obtained is set forth as SEQ ID NO:1.

Assays for binding of human neutrophils and HL-60 cells to porcine E-selectin transfected COS cells: COS7 cells (Designation CRL 1651, ATCC, Rockville, Md.) were transiently transfected with either the eukaryotic expression vector pAPEX-1 alone or pAPEX-1 containing the full-lengthporcine E-selectin cDNA (pAPEX-1/pE-selectin Briefly, a 3.5 kb NotI-XhoI fragment (from plasmid vector porcine E-selectin/pBLUESCRIPT SK.sup.-) containing the porcine E-selectin cDNA was cloned into the NotI/XhoI sites of the polylinker in the expression vector pAPEX-1.

pAPEX-1 (SEQ ID NO:4) is a derivative of the vector pcDNAI/Amp (Invitrogen, San Diego Calif.) which was modified as follows to increase protein expression in mammalian cells. First, since the intron derived from the gene encoding the SV40 small-t antigen has been shown to decrease expression of upstream coding regions (Evans and Scarpulla, 1989), this intron was removed from pcDNAI/Amp by digestion with XbaI plus HvaI, followed by treatment with the Klenow fragment of DNA polymerase and all four dNTPs. The resulting blunt ended 4.2 kb fragment was gel purified and self ligated to yield a closed circular plasmid.

A 5'-untranslated region adenovirus/immunoglobulin hybrid intron was introduced into the plasmid by replacing a 0.5 kb NdeI-NotI fragment with the corresponding 0.7 kb NdeI-NotI fragment from the vector pRc/CMV7SB (obtained from Dr. Joseph Goldstein, University of Texas Southwest Medical Center, Dallas, Tex.). Finally, the resulting CMV promoter expression cassette was shuttled in an NdeI-SfiI fragment into the vector pGEM-4Z (Promega, Madison Wis.) by ligation to an NdeI-SfiI fragment (containing pGEM-4Z) obtained from a pGEM based expression vector containing a CMV-promoter and an SV40 origin of replication (Davis, et al., 1991).

COS-7 cells were transfected using the DEAE-dextran method. Briefly, COS-7 cells were plated at a density of 2.5.times.10.sup.6 cells per 100 mm tissue culture dish. The cells were transfected 24 hr later using 5 ml serum-free RPMI 1640 medium containing 0.4 mg/ml DEAE-dextran, 100 .mu.M chloroquine, 2 mM glutamine, 25 .mu.g/ml bovine insulin, 25 .mu.g/ml human transferrin, 25 ng/ml sodium selenite, and 1 .mu.g/ml DNA. After incubation at 37.degree. C. for 3.5 hr, the transfection medium was aspirated and replaced with 10% DMSO in PBS for 2 min. The cells were rinsed once with serum-free DMEM and then cultured for 24 hr in D10. On day 2, the cells were harvested using trypsin and plated in a 96 well plate at 1.times.10.sup.4 cells/well. The cells were assayed for the ability to bind human neutrophils and HL-60 cells on day 4 as described above.

Generation of vectors directing the expression of soluble porcine E-selectin: PCR was performed using the plasmid pAPEX-1/pEselectin (described above) as template and oligo 446 (SEQ ID NO:5) and oligo 483 (SEQ ID NO:6) as primers. The approximately 520 bp PCR product was purified using GENE CLEAN and digested with SphI plus EcoRI. The resulting approximately 275 bp band was gel purified and ligated into the vector pGEM-7Zf(+) (Promega, Madison Wis.) to yield the plasmid pGEM-7Zf(+)446/483. The sequence of the cloned fragment of the PCR product was verified by the Sanger dideoxy chain termination method to contain the sequence set forth below as SEQ ID NO:7.

The vector pAPEX-3/spE-selectin+His (directing the expression of soluble porcine E-selectin containing a carboxyl terminal tag of six histidine residues to facilitate purification by nickel affinity chromatography) was constructed by ligating together: a 8973 bp NotI/Sse8337I fragment obtained from pAPEX-3/pE-selectin, a 1551 bp NotI/SphI fragment from pAPEX-3/pE-selectin, and a 264 bp SphI/Sse8337I fragment from pGEM7Zf(+)446/483.

Vector pAPEX-3/pE-selectin was constructed by a three-way ligation of a 4851 bp MluI/XhoI fragment from the vector pAPEX-1/pE-selectin (described above) with a 1144 bp MluI/SI fragment from pDR2b and a 6735 bp SpeI/SalI fragment from APEX-3.

Vector pAPEX-3 (SEQ ID NO:8) was constructed by a three-way ligation of a 1041 bp MluI/BamHI fragment of vector pRc/CMV7SC (obtained from Dr. Joseph Goldstein, University of Texas Southwest Medical Center, Dallas, Tex.; an identical fragment, corresponding to nucleotides 1 to 1041 of SEQ ID NO:4, may be obtained from vector pRc/CMV7SB, referred to above) ligated with a 6747 BamHI/SpeI fragment and a 1144 bp MluI/SpeI fragment, each obtained from vector pDR2b.

Vector pDR2b was constructed by self-ligation of an 8343 bp DNA fragment which was purified by gel electrophoresis after ClaI/AccI digestion of vector pDR2 (Promega Corporation, Madison, Wis.) and treatment of the digestion products with the Klenow fragment of DNA polymerase and all four dNTPs to produce blunt ends.

Vector pAPEX-3 (SEQ ID NO:8, discussed above) contains a CMV promoter followed by a hybrid adenovirus/immunoglobulin intron followed by a polylinker cloning site followed by an SV40 virus polyadenylation sequence. Additionally, APEX-3 contains a gene cassette conferring hygromycin B resistance to mammalian cells, and the Epstein Barr virus origin of replication (oriP) to allow replication and maintenance as a stable episome in cells expressing Epstein Barr virus nuclear antigen (EBNA).

Generation of stabily transfected cells secreting porcine E-selectin. 293-EBNA cells, (Invitrogen, San Diego, Calif.) were maintained in medium A (Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 10% (v/v) heat-inactivated fetal calf serum, 100 U/mL penicillin, and 100 ug/ml streptomycin) containing 250 .mu.g/ml G-418. On day 0, cells were plated at 1.0.times.10.sup.6 cells per 60 mm dish. On day 1, the cells were washed twice with DMEM, and refed 0.5 ml DMEM.

TRANSFECTAM reagent (15 .mu.L, Promega Corporation, Madison, Wis.) was added to 0.5 mL DMEM and mixed by pipetting. This TRANSFECTAM in DMEM mixture was next added to 5 ug DNA (pAPEX-3/spE-selectin+His) in 0.5 ml DMEM, mixed by pipetting, and the total 1 mL volume was added to a plate of cells. After incubation for 4 hours at 37.degree. C., the dishes were washed twice with DMEM and refed medium A. On day 2, the cells were refed medium A supplemented with 250 .mu.g/ml G-418 and 300 U/ml hygromycin B. After 7 days all surviving cells were pooled and maintained as cell line 50-A2.

Purification and characterization of soluble porcine E-selectin protein. 50-A2 cells from one confluent 175 cm.sup.2 flask were seeded into ten 175 cm.sup.2 flasks in 30 mL medium B (medium A containing 250 .mu.g/ml G-418 plus 300 U/ml hygromycin B). The cells were grown to confluence over 7 days with one refeeding. The conditioned medium B was stored at 4.degree. C. until purification. When cells reached confluence, they were refed 30 mL EX-CELL 300 medium (JRH Biosciences, Lexena, Kans.) every 3 to 4 days for a total of 14 days.

Several purification runs were performed, each using 600 ml of conditioned medium B or conditioned EX-CELL 300 medium. The 600 mL of medium was concentrated using a stirred cell fitted with a YM10 membrane (Amicon, Inc., Beverly, Mass.) to a final volume of approximately 50 mL.

Nickel charged resin was prepared by washing iminodiacetic acid/sepharose 6B fast flow resin (Sigma Chemical Company, St. Louis, Mo.) with 7 volumes each of: 1) water; 2) 50 mM NiSO.sub.4 ; and 3) buffer B (20 mM Tris, 500 mM NaCl, 5 mM imidazole, pH 8.0). Each wash was for 30 minutes with rocking to maintain the resin in suspension, followed by centrifugation at 1000 rpm for 5 minutes to pellet the resin.

For binding of the histidine tagged soluble porcine E-selectin, 25 mL concentrated medium was mixed with 3.5 ml 8.times. buffer B and approximately 1 ml packed volume of NiSO.sub.4 charged resin. The medium was incubated for 90 minutes at room temperature with rocking. The resin was removed by centrifugation, and washed twice with 20 ml buffer B. The resin was next resuspended in 10 ml buffer B and poured into a column (BioRad Laboratories, Hercules, Calif.). The column (2 mL settled resin volume) was washed with 35 column volumes buffer B followed by 20 column volumes buffer W (20 mM Tris, 500 mM NaCl, 30 mM imidazole, pH 8.0). Finally, the bound protein was eluted with 4 column volumes of buffer E (20 mM Tris, 500 mM NaCl, 1 M imidazole, pH 8.0).

The eluted material was dialyzed at 4.degree. C. against Hank's balanced salt solution (HBSS) using MWCO=3500 dialysis tubing. Analysis of the eluted material was performed by polyacrylamide gel electrophoresis from multiple batches and staining with Coomassie blue.

ELISA screen for anti-porcine E-selectin antibodies: To test antibodies for reactivity with porcine E-selectin, an ELISA was carried out using the following protocol:

A 50 .mu.L aliquot of a solution of soluble porcine E-selectin in sodium carbonate/bicarbonate buffer, pH 9.5, was incubated overnight at 4.degree. C. in each test well of a 96 well plate (Nunc-Immuno F96 Polysorp, A/S Nunc, Roskilde, Denmark) in order to bind the protein to the plastic plate. The wells were then subjected to a wash step. (Each wash step consisted of three washes with TBST.) Next, test wells were blocked with 200 .mu.L of blocking solution, 1% BSA in TBS (BSA/TBS), for 1 hour at 37.degree. C. (or, in some cases, 4.degree. C. overnight). After an additional wash step, a 50 .mu.L aliquot of test antibody solution (e.g., hybridoma supernatant) was incubated in each test well for 1 hour at 37.degree. C. with a subsequent wash step.

As a secondary (detection) antibody, 50 .mu.L of a 1:2000 dilution of horseradish peroxidase (HRP) conjugated goat anti-mouse IgG in BSA/TBS was incubated in each test well for 1 hour at 37.degree. C., followed by a wash step. Following the manufacturer's procedures, 10 mg of O-phenylenediamine (Sigma Chemical Company, St. Louis, Mo., Catalog No. P-8287) was dissolved in 25 mLs of phosphate-citrate buffer (Sigma Chemical Company, St. Louis, Mo., Catalog No. P-4922), and 50 .mu.L of this substrate solution was added to each well to allow detection of peroxidase activity. Finally, to stop the peroxidase detection reaction, a 50 .mu.L aliquot of 3N hydrochloric acid was added to each well. The presence of antibodies reactive with porcine E-selectin in the test antibody solutions was read out by a spectrophotometric OD determination at 490 nm.

The solution of soluble porcine E-selectin in sodium carbonate/bicarbonate buffer that served as a source of the protein bound to the plastic plate was used at 2-fold serial dilutions across the plate starting at 50 .mu.g of porcine E-selectin per mL, i.e., at 50, 25, 12.5, 6.25, 3.125, 1.5625, and 0.78125 .mu.g/mL. These dilutions were used to determine the minimum amount of soluble porcine E-selectin that would give maximum sensitivity in this assay. This amount was determined to be the 1.5625 .mu.g/mL dilution.

Northern blot analysis of E-selectin expression in porcine endothelial cells: PAEC were grown to confluence and incubated with D10 supplemented with human IL-1 (20 ng/ml) or TNF.alpha. (20 ng/ml) for 4 hr at 37.degree. C. Total RNA was isolated from the cytokine induced and uninduced PAEC as described above. Twenty micrograms from each RNA source was denatured in glyoxal, loaded on a 2% agarose gel in 10 mM phosphate and electrophoresed for 5 hr at 75 volts. RNA was transferred to nitrocellulose (Schleicher and Schuell, Kenne N.H.) by capillary action in 20.times. SSC. The membrane was prehybridized in BSA/SDS buffer for 2 hr at 650C and subsequently hybridized overnight at 60.degree. C. in the same buffer with a .sup.32 P-labeled probe containing most of the porcine E-selectin coding region as a 1.6Kbp BamHI fragment of the pAPEX-1/pE-selectin plasmid referred to above (specific activity: 2.times.10.sup.9 CPM /.mu.g of DNA).

The blot was washed as follows: two-15 min washes with 2.times. SSC00.1% SDS at 23.degree. C., two-15 min washes with 0.5.times. SSC/0.1% SDS at 60.degree. C. and two-15 min washes with 0.2.times. SSC/0.1% SDS at 60.degree. C. Finally, the blot was exposed to film with intensifying screens for 8 hr at -80.degree. C. The membrane was subsequently stripped in 0.1.times. SSC at 65.degree. C. for 1 hr before reprobing with a human .alpha.-tubulin probe (ATCC #37795) following the procedures described above for probing with the porcine E-selectin coding region probe.

EXAMPLE 1

Molecular Cloning and Sequence Analysis of Porcine E-Selectin

E-selectin homologues have been cloned and characterized from several species including human, mouse, rabbit, cow, and rat (Bevilacqua, et al., 1989; Weller, et al., 1992; Larigan, et al., 1992; and Fries, et al., 1993). Alignment of E-selectin amino acid sequences from several of these species reveals several regions of shared amino acid identity. Two degenerate oligonucleotides were designed based on sequence homology within the human and mouse E-selectin lectin-like domains. These oligonucleotides were used to PCR amplify the 150 bp fragment referred to above from PAEC cDNA. Analysis of this fragment revealed a unique sequence that was approximately 80% identical to the lectin domains of human and mouse E-selectins.

This 150 bp fragment was used to probe a human cytokine-stimulated PAEC cDNA library and multiple hybridizing clones were obtained. Sequence analysis of a 3.4 kb putative full-length clone revealed 1.9 kb of 3' untranslated DNA and an open reading frame of 1452 nucleotides encoding 484 amino acids (SEQ ID NO:1). Comparison of the predicted amino acid sequence of the porcine molecule with human E-selectin revealed an overall amino acid identity of 75%, while comparison to human P selectin revealed an identity of 44%.

Based on this information, this clone was designated as porcine E-selectin. Analysis of the porcine E-selectin structural domains also revealed homology to human E-selectin including a short signal peptide followed by lectin-like and EGF domains, complement repeats, a short hydrophobic transmembrane domain and a cytoplasmic tail (FIG. 1). The structure of porcine E-selectin differed from that of human E-selectin in that the porcine protein contained only four complement repeats whereas the human protein contained six such repeats. Based on sequence comparison, this divergence appears to have resulted from a deletion of complement repeats 1 and 4.

EXAMPLE 2

E-Selectin Mediated Binding of Human Cells to PAEC

Binding assays were performed between PAEC and human neutrophils or HL-60 cells (FIG. 2). Human neutrophils bound weakly to untreated porcine endothelial cells. However, treatment of PAEC with human TNF.alpha. resulted in a marked increase in human neutrophil and HL-60 adhesion (15-20 fold) while induction of PAEC with human IL-1 resulted in only a slight increase in the binding (2 fold) of these cells.

Pre-treatment of human neutrophils and HL-60 cells with neuraminidase completely blocked their adhesion to PAEC, suggesting that sialic acid residues were required for these interactions. Binding assays performed in the presence of a blocking antibody against human LFA-1 failed to inhibit cell adhesion, suggesting that this molecule does not play a significant role in the interactions between PAEC and human neutrophils or HL-60 cells under these assay conditions. Taken together, these data indicate that PAEC express a cytokine inducible cell surface receptor that mediates binding to human neutrophils and HL-60 cells. Further, the requirement for sialic acid, together with the sequence comparisons set forth above in Example 1 and in FIG. 1, indicates that this receptor is functionally and structurally similar to human E-selectin.

EXAMPLE 3

Human Neutrophils and HL-60 Cells Bind to Recombinant E-Selectin Expressed in COS Cells

The binding of purified human neutrophils to control transfected, and porcine E-selectin transfected COS cells was analyzed. These experiments were undertaken in order to determine whether porcine E-selectin directly mediates the increased human neutrophil and HL-60 binding to PAEC seen upon stimulation of PAEC with human TNF.alpha. and to test whether sialic acid residues on these cells play a critical role in this increased binding.

The results of these studies are presented in FIG. 3. Increased binding (4-5 fold) was observed between human neutrophils or HL-60 cells and COS cells transfected with porcine E-selectin (i.e., pAPEX-1/pE-selectin) as compared to COS cells transfected with vector alone (i.e. the APEX-1 expression vector without the porcine E-selectin encoding insert). As was demonstrated for the binding of human neutrophils and HL-60 to cytokine-induced PAEC, the binding to porcine E-selectin transfected COS cells was completely blocked by prior incubation of human neutrophils with neuraminidase, thereby confirming that sialic acid residues expressed on human leukocytes are required for binding to porcine E-selectin.

Additional binding studies were carried out in the presence of the divalent ion chelating agent EDTA or the relatively calcium ion specific chelating agent EGTA. Since sialic acid mediated binding requires the presence of free calcium ions, inhibition of binding by these chelating agents provides additional evidence for the involvement of sialic acid in these binding interactions.

EXAMPLE 4

Human TNF.alpha. Induces Porcine E-Selectin Gene Transcription

Previous studies have shown that human E-selectin gene transcription is induced by the human cytokines TNF.alpha. and IL-1, as well as by bacterial lipopolysaccharide (LPS) (Bevilacqua, et al., 1989; and Montgomery, et al., 1991). Induction of E-selectin expression on human endothelial cells occurs within 3-4 hours after cytokine stimulation and returns to background levels after 16-24 hours (Bevilacqua, et al., 1989). As described above, there was a dramatic (15-20 fold) increase in neutrophil binding after stimulation of PAEC with human TNF.alpha. but only a minimal increase after stimulation with human IL-1 (FIG. 2). Studies were undertaken to determine if this differential inducibility of PAEC binding correlates with levels of PAEC porcine E-selectin gene transcription.

Northern blots were performed on RNA derived from uninduced PAEC and PAEC induced with either human TNF.alpha. or human IL-1 using the full-length porcine E-selectin cDNA as a probe. Hybridization of the porcine E-selectin probe to RNA derived from either unstimulated or human IL-1 stimulated PAEC was not observed. By contrast, the porcine E-selectin probe strongly hybridized to a single RNA species of approximately 3.4 kb derived from human TNF.alpha. stimulated PAEC. This band corresponded to the size of the full-length porcine E-selectin cDNA clone isolated from the PAEC library. When probed with the control .alpha.-tubulin probe, the same blot showed equivalent levels of hybridization to RNA derived from unstimulated PAEC, human IL-1 stimulated PAEC, or human TNF.alpha. stimulated PAEC.

These data parallel the differential effect of human TNF.alpha. and IL-1 on human neutrophil/PAEC binding and suggest that porcine E-selectin plays a critical role in the binding of neutrophils to xenograft vascular endothelium in vivo.

EXAMPLE 5

Characterization of Anti-E-Selectin Antibodies

Anti-human-E-selectin monoclonal antibodies were obtained as follows: A commercial anti-human-E-selectin monoclonal antibody ("anti-Elam-1" clone H18/7) was obtained from Collaborative Biomedical Products, Becton Dickenson Labware (Bedford, Mass., Catalog #550023). Anti-human-E-selectin monoclonal antibodies from clones CL-2, CL-3, and CL-37, were obtained from Dr. C. Wayne Smith, Baylor Clinical Care Center, Houston, Tex. (see Mulligan et al. 1991). These antibodies were tested by FACS against PAEC treated with 25ng/ml TNF.alpha., PAEC treated with long/ml IL-1, or untreated PAEC. Only CL-37 bound to the TNF.alpha. treated PAEC, and none of the antibodies bound to IL-1 treated or untreated PAEC. CL-37 was also tested and found by FACS analysis to bind to porcine E-selectin expressing COS cells, but not to untransfected COS cells. CL-37 was also shown to bind to soluble porcine E-selectin using the ELISA described above.

EXAMPLE 6

Soluble Porcine E-Selectin

Soluble recombinant porcine E-selectin, prepared as described above, migrated by PAGE as a single Coomassie stained band with an apparent molecular weight of 66 kDa. Since the apparent molecular weight of the soluble porcine E-selectin molecule is higher than would be predicted from its amino acid sequence, it is evident that the molecule is glycosylated.

As discussed in the preceding example, the soluble porcine E-selectin molecule reacted specifically with the anti-human-E-selectin antibody CL-37.

Deposits

Plasmid porcine E-selectin/pBLUESCRIPT SK.sup.- was deposited with the American Type Culture Collection, 12301 Parklawn Drive, Rockville, Md., 20852, United States of America, in E. coli strain SOLR on May 6, 1994, and has been assigned the designation number ATCC 69616. This deposit was made under the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure (1977).

Although preferred and other embodiments of the invention have been described herein, a variety of modifications which do not depart from the scope and spirit of the invention will be evident to persons of ordinary skill in the art from this disclosure. The following claims are intended to cover the specific embodiments set forth herein as well as such modifications, variations, and equivalents.

REFERENCES

Allen, et al., 1993. Circulation 88, pp. 243. Ammerer, 1983. Meth Enzymol 101, pp. 192. Auchincloss, 1988. Transplantation 46, pp. 1. Ausubel, et al., 1992. Current Protocols in Mol Bio, John Wiley & Sons, New York. Berg, et al., 1991. J Biol Chem 23, pp. 14869. Bevilacqua and Nelson, 1993. J Clin Invest 91, pp. 379. Bevilacqua, et al., 1989. Science 243, pp. 1160. Bradley, in Robertson (ed), 1987. Teratocarcinomas and Embryonic Stem Cells a Practical Aoproach. IRL Press, Eynsham, Oxford, England. Brinster, et al., 1985. Proc Natl Acad Sci 82, pp. 4438-4442. Brinster, et al., 1989. Proc Natl Acad Sci 86, pp. 7087-7091. Brockmeyer, et al., 1993. Transplantation 55, pp. 610. Capecchi, 1989. Trends in Genetics 5(3)pp. 70-76. Carlos, et al., 1991. Blood 77, pp. 2266. Carson, et al., 1993. J Rheumatol 20, pp. 809. Chang, et al., 1978. Nature 275, pp. 615. Chomczynski and Sacchi, 1987. Analytical Biology 162, pp. 156. Clackson, et al., 1991. Nature 352, pp. 624-628. Cohen, 1989. Oligodeoxynucleotides, Antisense Inhibitors of Gene Expression, CRC Press, Inc., Boca Raton, Fla. Church and Gilbert, 1984. Proc Natl Acad Sci 81, pp. 1991. Coligan, et al., 1992. Current Protocols in Immunol, John Wiley & Sons, New York. Cotran, et al., 1986. J Exy Med 164, pp. 661. Dalmasso, et al., 1992. Am J Path 140, pp. 1157. Davis, et al., 1991. Science 253, pp. 59. Deutscher (ed), 1990. Guide to Protein Purification, Volume 182. Academic Press, Inc., San Diego, Calif. Eguchi, et al., 1991. Annu Rev Biochem 60, pp. 631-652. Evans and Scarpulla, 1989. Gene 84, pp. 135. Ferran, et al., 1993. Transplantation 55, pp. 605. Fries, et al., 1993. Am Journ Pathol 143:, pp. 725. Frohman and Martin, 1989. Cell 56, pp. 145-147. Gearing and Newman, 1993. Immunol Today 14(10), pp. 506. Gearing, et al., 1992. Annals NY Acad Sci 667, pp. 324. Georas, et al., 1992. Am J Respir Cell Mol Biol 7, pp. 261. Goeddel, et al., 1980. Nucl Acids Res 8, pp. 4057. Goeddel (ed), 1990. Gene Expression Technology, Volume 185. Academic Press, Inc., San Diego, Calif. Gossler, et al., 1986. Proc Natl Acad Sci 83, pp. 9065-9069. Graber, et al., 1990. J Immunol 145, pp. 819. Haber, 1992. Immunol Rev 130, pp. 189-212. Hakkert, et al., 1991. Blood 78, pp. 2721. Harlow and Lane, 1988. Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. Harris and Angal (eds), 1989. Protein Purification Methods: A Practical Approach. IRL Press, Oxford University Press, Oxford. Hasty, et al., 1991. Mol Cell Bio 11(11), pp. 5586-5591. Hogan, et al., 1986. Manipulating the Mouse Embryo: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. Hviid, et al., 1994. Immunol Letts. (In press). Jasin and Berg, 1988. Genes & Development 2, pp. 1353-1363. Jeannotte, et al., 1991. Mol Cell Bio 11(11), pp. 557814 5585. Koch, et al., 1991. Lab Invest 64, pp. 313. Kuijpers, et al., 1991. J Immunol 147, pp. 1369. Larigan, et al., 1992. DNA Cell Biol 206, pp. 401. Lasky, 1992. Science 258, pp. 964. Leeuwenberg, et al., 1992. Immunology 77, pp. 543. Leventhal, et al., 1993. Transplantation 55, pp. 857. Lidell and Cryer, 1991. A Practical Guide To Monoclonal Antibodies. John Wiley & Sons, Chichester, West Sussex, England. Lo, et al., 1991. J E=Med 173, pp. 1493. Lobb, et al., 1991. J Immunol 147, pp. 124. Lovell-Badge, in Robertson (ed), 1987. Teratocarcinomas and Embryonic Stem Cells a Practical Approach. IRL Press, Eynsham, Oxford, England. Luckow, et al., 1988. Bio/Technology 6, pp. 47. Makowka, et al., Sep. 1993. Second International Congress on Xenotransplantation, Cambridge, England, abstract 4. Maniatis, 1982. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., pp. 412. Mansour, et al., 1988. Nature 336, pp. 348-352. McMahon, et al, 1990. Cell 62, pp. 1073-1085. Mejia-Laguna, et al., 1972. Am Journ Pathol 69, pp. 71. Moir, et al., 1991. Meth Enzymol 194, pp. 491-507. Mollnes, et al., 1988. Scand J Immunol 28, pp. 307-312. Montgomery, et al., 1991. Proc Natl Acad Sci 88, pp. 6523. Montz, et al., 1990. Cellular Immunol 127, pp. 337-351. Morrison, 1992. Annu Rev Immunol 10, pp. 239-265. Mortensen, et al., 1992. Mol Cell Bio 12(5), pp. 2391-2395. Muler-Eberhard, 1988. Ann Rev Biochem 57, pp. 321. Mulligan, et al., 1991. J Clin Invest 88, pp. 1396. Mulligan, et al., 1993. J Immunol 151, pp. 6410. Najarian, 1992. Transplant Proc 24, pp. 733. Newman, et al., 1993. J Immunol 150, pp. 633. Pedersen, et al., 1990. Transgenic Techniques in Mice--A Video Guide. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. Picker, et al., 1991. Nature 349, pp. 796. Pigott, et al., 1992. Biochem Biophys Res Commun 187, pp. 584. Pruitt, et al., 1991. Transplantation 52, pp. 868. Redi, et al., 1991. Am J Pathol 139, pp. 461. Reichmann, et al., 1988. Nature 332, pp. 323-327. Remington's Pharmaceutical Sciences. 17th Ed., 1985. Mack Publishing Company, Philadelphia, Pa. Robertson, et al., 1986. Nature 323, pp. 445-448. Robertson, in Robertson (ed), 1987. Teratocarcinomas and Embryonic Stem Cells a Practical Approach. IRL Press, Eynsham, Oxford, England. Rodrigues, et al., 1993. J Immunol 151, pp. 6954-6961. Sambrook, et al., 1989. Molecular Cloning: A Laboratory Manual, 2nd Ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. Sanger, et al., 1977. Proc Natl Acad Sci 74, pp. 5463. Satake, et al., Sep. 1993. Second International Congress on Xenotransplantation, Cambridge, England, abstract 126. Schena, et al., 1991. Meth Enzymol 194, pp. 389-398. Shimuzu, et al., 1991. Nature 349, pp. 799. Somervile and d'Apice, 1993. Kidney Intl 44, pp. 112. Taylor, et al., 1992. Transplantation 54, pp. 451. Thomas, et al., 1986. Cell 44(3), pp. 419-428. Thomas, et al., 1987. Cell 51(3), pp. 503-512. Thomas, et al., 1992. Mol Cell Bio 12(7), pp. 2919-2923. Tibell, et al., Sep. 1993. Second International Congress on Xenotransplantation, Cambridge, England, abstract 64. Tuso, et al., 1993. Transplantation 55, pp. 1375. Tyrrell, et al., 1991. Proc Natl Acad Sci 88, pp. 10372. Vercellotti, et al., 1991. J Immunol 146, pp. 730. Weller, et al., 1992. J Biol Chem 267, pp. 15176. Winter and Milstein, 1991. Nature 349, pp. 293-299. Wurzner, et al., 1991. Complement Inflamm 8, pp. 328-340. Zehr, et al., 1994. Transplantation 57, pp. 900. TABLE 1______________________________________BLOOD LEVELS OF CIRCULATINGSOLUBLE E-SELECTINLEVEL IN HEALTHY INDIVIDUALS22 .+-. 12 ng/ml (n = 62)0.9 .+-. 0.7 ng/ml (n = 71)48 .+-. 19 ng/ml (n = 64)16 (range 9-42) ng/ml (n = 89)22-75 ng/ml (n = 15)FOLD ELEVATION IN DISEASEx 2 Diabetesx 2 Breast/gastro-intestinal cancerx 3-x 9 Septic shockx 23 Septic shockx 4 Systemic lupus erythematosusx 2 Sclerodermax 2 Giant cell arteritisx 2 Polyarteritis nodosax 2 Malaria______________________________________ __________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 9- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1592 ba - #se pairs (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Doub - #le (D) TOPOLOGY: Linear- (ii) MOLECULE TYPE: cDNA to mRNA (A) DESCRIPTION: Porci - #ne E-selectin- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #1:# 50GCAAGA GGCACGAAGC AAGCCAGAGC AACACAGGAN# 100GATAAA CACTTCACAA AACCAAAAGC ATTTCAAGTC#CAG 146A CTCTTGAAGT C ATG ATT GCT TCA# Met - # Ile Ala Ser Gln20- TTT CTC TCT GCT CTC CCT TTG GTG CTT CTC CT - #G CTT AGA GAA# 188Phe Leu Ser Ala Leu Pro Leu Val Leu Leu Le - #u Leu Arg Glu- AGT GGA GCC TGG TCT TAC AGC GCC TCT ACA GA - #A ACC ATG ACT# 230Ser Gly Ala Trp Ser Tyr Ser Ala Ser Thr Gl - #u Thr Met Thr# 10- TTT GAT GAT GCC AGT GCT TAT TGC CAG CAG AG - #G TAC ACA CAT# 272Phe Asp Asp Ala Ser Ala Tyr Cys Gln Gln Ar - #g Tyr Thr His# 25- CTG GTC GCA ATT CAA AAC CAT GCA GAG ATT GA - #A TAC CTG AAC# 314Leu Val Ala Ile Gln Asn His Ala Glu Ile Gl - #u Tyr Leu Asn# 35- TCC ACG TTC AAC TAT TCA GCA AGT TAC TAC TG - #G ATT GGA ATC# 356Ser Thr Phe Asn Tyr Ser Ala Ser Tyr Tyr Tr - #p Ile Gly Ile#50- AGG AAG ATC AAT GGT ACA TGG ACA TGG ATA GG - #G ACC AAG AAG# 398Arg Lys Ile Asn Gly Thr Trp Thr Trp Ile Gl - #y Thr Lys Lys# 65- GCC TTG ACC CCA GAG GCC ACC AAC TGG GCT CC - #A GGT GAA CCA# 440Ala Leu Thr Pro Glu Ala Thr Asn Trp Ala Pr - #o Gly Glu Pro# 80- AAT AAT AAG CAA AGC AAT GAG GAC TGT GTA GA - #G ATC TAC ATC# 482Asn Asn Lys Gln Ser Asn Glu Asp Cys Val Gl - #u Ile Tyr Ile# 95- AAG AGA GAC AAG GAC TCG GGC AAG TGG AAT GA - #T GAG AGA TGC# 524Lys Arg Asp Lys Asp Ser Gly Lys Trp Asn As - #p Glu Arg Cys# 105- AGC AAA AAG AAG CTC GCC TTG TGC TAC ACA GC - #T GCC TGT ACC# 566Ser Lys Lys Lys Leu Ala Leu Cys Tyr Thr Al - #a Ala Cys Thr110 1 - #15 1 - #20- CCT ACA TCC TGC AGC GGC CAT GGT GAA TGC AT - #A GAG ACC ATC# 608Pro Thr Ser Cys Ser Gly His Gly Glu Cys Il - #e Glu Thr Ile# 135- AAT AGC TCT ACT TGC CAG TGC TAC CCC GGC TT - #C CGA GGC CTC# 650Asn Ser Ser Thr Cys Gln Cys Tyr Pro Gly Ph - #e Arg Gly Leu# 150- CAG TGT GAG CAA GTG GTT GAG TGT GAT GCT TT - #G GAA AAT CCT# 692Gln Cys Glu Gln Val Val Glu Cys Asp Ala Le - #u Glu Asn Pro# 165- GTC AAC GGA GTC GTG ACA TGT CCC CAA AGC CT - #C CCA TGG AAC# 734Val Asn Gly Val Val Thr Cys Pro Gln Ser Le - #u Pro Trp Asn# 175- ACA ACC TGT GCA TTT GAG TGT AAG GAA GGA TT - #T GAA CTC ATT# 776Thr Thr Cys Ala Phe Glu Cys Lys Glu Gly Ph - #e Glu Leu Ile180 1 - #85 1 - #90- GGA CCT GAG CAC CTG CAA TGT ACC TCA TCT GG - #G AGC TGG GAC# 818Gly Pro Glu His Leu Gln Cys Thr Ser Ser Gl - #y Ser Trp Asp# 205- GGC AAG AAG CCA ACG TGT AAA GCT GTG ACA TG - #T GAC ACC GTC# 860Gly Lys Lys Pro Thr Cys Lys Ala Val Thr Cy - #s Asp Thr Val# 220- GGC CAT CCT CAG AAT GGT GAT GTG AGT TGT AA - #C CAC TCC TCT# 902Gly His Pro Gln Asn Gly Asp Val Ser Cys As - #n His Ser Ser# 235- ATT GGA GAG TTT GCC TAC AAG TCA ACC TGC CA - #C TTC ACC TGT# 944Ile Gly Glu Phe Ala Tyr Lys Ser Thr Cys Hi - #s Phe Thr Cys# 245- GCA GAA GGC TTC GGG CTG CAG GGG CCA GCC CA - #G ATT GAA TGC# 986Ala Glu Gly Phe Gly Leu Gln Gly Pro Ala Gl - #n Ile Glu Cys250 2 - #55 2 - #60- ACT GCC CAG GGG CAA TGG ACC CAG CAA GCC CC - #A GTT TGT AAA#1028Thr Ala Gln Gly Gln Trp Thr Gln Gln Ala Pr - #o Val Cys Lys# 275- GCT GTG AAA TGT CCT GCT GTC TCC CAG CCC AA - #G AAT GGC TTG#1070Ala Val Lys Cys Pro Ala Val Ser Gln Pro Ly - #s Asn Gly Leu# 290- GTG AAG TTT ACC CAT TCC CCG ACT GGA GAG TT - #T ACC TAC AAG#1112Val Lys Phe Thr His Ser Pro Thr Gly Glu Ph - #e Thr Tyr Lys# 305- TCC TCC TGT GCC TTC AGC TGT GAG GAA GGC TT - #T GAA TTA CGT#1154Ser Ser Cys Ala Phe Ser Cys Glu Glu Gly Ph - #e Glu Leu Arg# 315- GGA TCA GCT CAA CTT GCA TGC ACA TCT CAA GG - #A CAA TGG ACA#1196Gly Ser Ala Gln Leu Ala Cys Thr Ser Gln Gl - #y Gln Trp Thr320 3 - #25 3 - #30- CAG GAG GTT CCC TCC TGC CAA GTG GTA CAG TG - #T TCA AGT TTG#1238Gln Glu Val Pro Ser Cys Gln Val Val Gln Cy - #s Ser Ser Leu# 345- GAG GTT CCC AGA GAG ATC AAC ATG AGC TGC AG - #T GGG GAG CCC#1280Glu Val Pro Arg Glu Ile Asn Met Ser Cys Se - #r Gly Glu Pro# 360- GTG TTT GGT GCT GTG TGT ACA TTT GCC TGT CC - #T GAA GGA TGG#1322Val Phe Gly Ala Val Cys Thr Phe Ala Cys Pr - #o Glu Gly Trp# 375- ATG CTC AAT GGC TCT GTA GCT CTG ACG TGT GG - #T GCC ACA GGA#1364Met Leu Asn Gly Ser Val Ala Leu Thr Cys Gl - #y Ala Thr Gly# 385- CAC TGG TCT GGG ATG CTG CCT ACT TGT GAA GC - #T CCT GCT GAG#1406His Trp Ser Gly Met Leu Pro Thr Cys Glu Al - #a Pro Ala Glu390 3 - #95 4 - #00- TCC AAA ATT CCC TTG GCA ATG GGA CTT GCT GC - #T GGT GGA GTC#1448Ser Lys Ile Pro Leu Ala Met Gly Leu Ala Al - #a Gly Gly Val# 415- TCC TTC ATG ACA TCA GCA TCA TTT CTC CTC TG - #G CTC CTG AAA#1490Ser Phe Met Thr Ser Ala Ser Phe Leu Leu Tr - #p Leu Leu Lys# 430- CGC CTT CGG AAG AGA GCA AAA AAA TTT GTT CC - #T TCC AGC AGC#1532Arg Leu Arg Lys Arg Ala Lys Lys Phe Val Pr - #o Ser Ser Ser# 445- TCC GAA TGC CTT CAA CCC AAT GGA TCC TAC CA - #A ATG CCT TCT#1574Ser Glu Cys Leu Gln Pro Asn Gly Ser Tyr Gl - #n Met Pro Ser# 455#1592 CCAAAsp Leu Ile460- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 23 base - #s (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Sing - #le (D) TOPOLOGY: Linear- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: Oligo - #nucleotide primer- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #2:# 23TCMG RAA- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 29 base - #s (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Sing - #le (D) TOPOLOGY: Linear- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: Oligo - #nucleotide primer- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: Yes- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #3:# 29 CCAC RCAGTCCTC- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4059 ba - #se pairs (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Doub - #le (D) TOPOLOGY: Circular- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: Apex- - #1 Eukaryotic#Vector Expression- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #4:# 50ATTATT GACTAGTTAT TAATAGTAAT CAATTACGGG# 100GCCCAT ATATGGAGTT CCGCGTTACA TAACTTACGG# 150TGGCTG ACCGCCCAAC GACCCCCGCC CATTGACGTC# 200TTCCCA TAGTAACGCC AATAGGGACT TTCCATTGAC# 250TATTTA CGGTAAACTG CCCACTTGGC AGTACATCAA# 300AAGTAC GCCCCCTATT GACGTCAATG ACGGTAAATG# 350ATGCCC AGTACATGAC CTTATGGGAC TTTCCTACTT# 400GTATTA GTCATCGCTA TTACCATGGT GATGCGGTTT# 450TGGGCG TGGATAGCGG TTTGACTCAC GGGGATTTCC# 500TTGACG TCAATGGGAG TTTGTTTTGG CACCAAAATC# 550AAATGT CGTAACAACT CCGCCCCATT GACGCAAATG# 600ACGGTG GGAGGTCTAT ATAAGCAGAG CTCGTTTAGT# 650CTGTTG GGCTCGCGGT TGATTACAAA CTCTTCGCGG# 700TTGGAT CGGAAACCCG TCGGCCTCCG AACGGTACTC# 750CTGAGC GAGTCCGCAT CGACCGGATC GGAAAACCTC# 800GAGTAC TCCCTCTCAA AAGCGGGCAT GACTTCTGCG# 850TTCCAA AAACGAGGAG GATTTGATAT TCACCTGGCC# 900TGAGGG TGGCCGCGTC CATCTGGTCA GAAAAGACAA# 950AGCTTG AGGTGTGGCA GGCTTGAGAT CTGGCCATAC# 1000GACATC CACTTTGCCT TTCTCTCCAC AGGTGTCCAC# 1050GCAGGT CGACCGGCTT GGTACCGAGC TCGGATCCAC# 1100AGTGTG CTGGAATTCT GCAGATATCC ATCACACTGG# 1150TGCATC TAGAACTTGT TTATTGCAGC TTATAATGGT# 1200TAGCAT CACAAATTTC ACAAATAAAG CATTTTTTTC# 1250GTGGTT TGTCCAAACT CATCAATGTA TCTTATCATG# 1300GCCATG GTATCAACGC CATATTTCTA TTTACAGTAG# 1350TGTAGG TACCGCTGTA TTCCTAGGGA AATAGTAGAG# 1400CTGCAT CAGCCATATA GCCCCCGCTG TTCGACTTAC# 1450TACTGA CAAACCCATA CACCTCCTCT GAAATACCCA# 1500GTCTCC GAACTCATTA CACCCTCCAA AGTCAGAGCT# 1550AAGGGC AGCGAGGGCT TCTCCAGATA AAATAGCTTC# 1600TAAGGG TAGACACTTC AGCTAATCCC TCGATGAGGT# 1650AGTGCG GCTCCCATTT TGAAAATTCA CTTACTTGAT# 1700GGCGGA GGGCCTCCAA CACAGTAATT TTCCTCCCGA# 1750AATGTC AAGTCAGTTA AGCAGGAAGT GGACTAACTG# 1800GCGACA TCCTCTTTTA ATTAGTTGCT AGGCAACGCC# 1850TGGTTT TGCAAGAGGA AGCAAAAGCC TCTCCACCCA# 1900CCACCC AATCATTACT ATGACAACAG CTGTTTTTTT# 1950GGCCGG GGACCCCTGG GCCCGCTTAC TCTGGAGAAA# 2000TGTAGA GGCTTCCAGA GGCAACTTGT CAAAACAGGA# 2050GTCACA CTGTCTGGCC CTGTCACAAG GTCCAGCACC# 2100AATAAG CAGTTTGGGA ACGGGTGCGG GTCTTACTCC# 2150TAACTC CGCCCAGTTC CGCCCATTCT CCGCCCCATG# 2200TTTATT TATGCAGAGG CCGAGGCCGC CTCGGCCTCT# 2250GTAGTG AGGAGGCTTT TTTGGAGGCC TAGGCTTTTG# 2300CAGCAA AAGGCCAGGA ACCGTAAAAA GGCCGCGTTG# 2350TAGGCT CCGCCCCCCT GACGAGCATC ACAAAAATCG# 2400GGTGGC GAAACCCGAC AGGACTATAA AGATACCAGG# 2450AGCTCC CTCGTGCGCT CTCCTGTTCC GACCCTGCCG# 2500GTCCGC CTTTCTCCCT TCGGGAAGCG TGGCGCTTTC# 2550GTAGGT ATCTCAGTTC GGTGTAGGTC GTTCGCTCCA# 2600CACGAA CCCCCCGTTC AGCCCGACCG CTGCGCCTTA# 2650TCTTGA GTCCAACCCG GTAAGACACG ACTTATCGCC# 2700CTGGTA ACAGGATTAG CAGAGCGAGG TATGTAGGCG# 2750TTGAAG TGGTGGCCTA ACTACGGCTA CACTAGAAGG# 2800CTGCGC TCTGCTGAAG CCAGTTACCT TCGGAAAAAG# 2850GATCCG GCAAACAAAC CACCGCTGGT AGCGGTGGTT# 2900CAGCAG ATTACGCGCA GAAAAAAAGG ATCTCAAGAA# 2950TTCTAC GGGGTCTGAC GCTCAGTGGA ACGAAAACTC# 3000TGGTCA TGAGATTATC AAAAAGGATC TTCACCTAGA# 3050AAATGA AGTTTTAAAT CAATCTAAAG TATATATGAG# 3100CAGTTA CCAATGCTTA ATCAGTGAGG CACCTATCTC# 3150TTCGTT CATCCATAGT TGCCTGACTC CCCGTCGTGT# 3200CGGGAG GGCTTACCAT CTGGCCCCAG TGCTGCAATG# 3250ACGCTC ACCGGCTCCA GATTTATCAG CAATAAACCA# 3300CCGAGC GCAGAAGTGG TCCTGCAACT TTATCCGCCT# 3350AATTGT TGCCGGGAAG CTAGAGTAAG TAGTTCGCCA# 3400CAACGT TGTTGCCATT GCTACAGGCA TCGTGGTGTC# 3450GTATGG CTTCATTCAG CTCCGGTTCC CAACGATCAA# 3500TCCCCC ATGTTGTGCA AAAAAGCGGT TAGCTCCTTC# 3550TGTCAG AAGTAAGTTG GCCGCAGTGT TATCACTCAT# 3600TGCATA ATTCTCTTAC TGTCATGCCA TCCGTAAGAT# 3650GGTGAG TACTCAACCA AGTCATTCTG AGAATAGTGT# 3700TTGCTC TTGCCCGGCG TCAATACGGG ATAATACCGC# 3750CTTTAA AAGTGCTCAT CATTGGAAAA CGTTCTTCGG# 3800AGGATC TTACCGCTGT TGAGATCCAG TTCGATGTAA# 3850CAACTG ATCTTCAGCA TCTTTTACTT TCACCAGCGT# 3900AAACAG GAAGGCAAAA TGCCGCAAAA AAGGGAATAA# 3950TGTTGA ATACTCATAC TCTTCCTTTT TCAATATTAT# 4000GGGTTA TTGTCTCATG AGCGGATACA TATTTGAATG# 4050AACAAA TAGGGGTTCC GCGCACATTT CCCCGAAAAG# 4059- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 24 base - #s (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Sing - #le (D) TOPOLOGY: Linear- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: Oligo - #nucleotide primer- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #5:# 24AGTC AACC- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 58 base - #s (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Sing - #le (D) TOPOLOGY: Linear- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: Oligo - #nucleotide primer- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: Yes- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #6:# 50GGTTAA TGGTGATGGT GATGGTGTTT GGACTCAGCA# 58- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 275 bas - #e pairs (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Doub - #le (D) TOPOLOGY: Circular- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: pGEM- - #7Zf(+)446/483 insert- (iii) HYPOTHETICAL: No- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #7:# 50GGACAA TGGACACAGG AGGTTCCCTC CTGCCAAGTG# 100TTTGGA GGTTCCCAGA GAGATCAACA TGAGCTGCAG# 150TTGGTG CTGTGTGTAC ATTTGCCTGT CCTGAAGGAT# 200TCTGTA GCTCTGACGT GTGGTGCCAC AGGACACTGG# 250TACTTG TGAAGCTCCT GCTGAGTCCA AACACCATCA# 275 GCAG GAATT- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8932 ba - #se pairs (B) TYPE: Nucleic A - #cid (C) STRANDEDNESS: Doub - #le (D) TOPOLOGY: Circular- (ii) MOLECULE TYPE: Other nucleic aci - #d (A) DESCRIPTION: Apex- - #3 Eukaryotic#Vector Expression- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #8:# 50ACAAAA GCGCCCCTCG TACCAGCGAA GAAGGGGCAG# 100GGTTTA GTTCGTCCGG CGGCGGGGGA TCTGTATGGT# 150ATCTGC TCTGATGCCG CATAGTTAAG CCAGTATCTG# 200GTTGGA GGTCGCTGAG TAGTGCGCGA GCAAAATTTA# 250AAGGCT TGACCGACAA TTGCATGAAG AATCTGCTTA# 300GCGCTG CTTCGCGATG TACGGGCCAG ATATACGCGT# 350GACTAG TTATTAATAG TAATCAATTA CGGGGTCATT# 400ATATGG AGTTCCGCGT TACATAACTT ACGGTAAATG# 450CCGCCC AACGACCCCC GCCCATTGAC GTCAATAATG# 500AGTAAC GCCAATAGGG ACTTTCCATT GACGTCAATG# 550GGTAAA CTGCCCACTT GGCAGTACAT CAAGTGTATC# 600CCCCCT ATTGACGTCA ATGACGGTAA ATGGCCCGCC# 650GTACAT GACCTTATGG GACTTTCCTA CTTGGCAGTA# 700TCATCG CTATTACCAT GGTGATGCGG TTTTGGCAGT# 750GGATAG CGGTTTGACT CACGGGGATT TCCAAGTCTC# 800CAATGG GAGTTTGTTT TGGCACCAAA ATCAACGGGA# 850GTAACA ACTCCGCCCC ATTGACGCAA ATGGGCGGTA# 900GAGGTC TATATAAGCA GAGCTCGTTT AGTGAACCGT# 950GCTCGC GGTTGATTAC AAACTCTTCG CGGTCTTTCC# 1000GGAAAC CCGTCGGCCT CCGAACGGTA CTCCGCCACC# 1050AGTCCG CATCGACCGG ATCGGAAAAC CTCTCGACTG# 1100CCCTCT CAAAAGCGGG CATGACTTCT GCGCTAAGAT# 1150AACGAG GAGGATTTGA TATTCACCTG GCCCGCGGTG# 1200GGCCGC GTCCATCTGG TCAGAAAAGA CAATCTTTTT# 1250GGTGTG GCAGGCTTGA GATCTGGCCA TACACTTGAG# 1300ACTTTG CCTTTCTCTC CACAGGTGTC CACTCCCAGG# 1350GACCGG CTTGGTACCG AGCTCGGATC CTCTAGAGTC# 1400CAAGCT TGGCACTGGC CGTCGTTTTA CAACGTCGTG# 1450GGCGTT ACCCAACTTA ATCGCCTTGC AGCACATCCC# 1500GCGTAA TAGCGAAGAG GCCCGCACCG ATCCAGACAT# 1550ATGAGT TTGGACAAAC CACAACTAGA ATGCAGTGAA# 1600TGTGAA ATTTGTGATG CTATTGCTTT ATTTGTAACC# 1650TAAACA AGTTAACAAC AACAATTGCA TTCATTTTAT# 1700GGGAGG TGTGGGAGGT TTTTTAAAGC AAGTAAAACC# 1750ATGGCT GATTATGATC CCCAGGAAGC TCCTCTGTGT# 1800ACCTCC TCTACTTGAG AGGACATTCC AATCATAGGC# 1850CTGTGT CCTCCTGTTA ATTAGGTCAC TTAACAAAAA# 1900GGTTTT TCACAGACCG CTTTCTAAGG GTAATTTTAA# 1950CCCTTC CACTGCTGTG TTCCAGAAGT GTTGGTAAAC# 2000AACAGC AGAAACATAC AAGCTGTCAG CTTTGCACAA# 2050GCTCAT CAAGAAGCAC TGTGGTTGCT GTGTTAGTAA# 2100GGCACA TTTTCCCCAC CTGTGTAGGT TCCAAAATAT# 2150TTTACT TGGATCAGGA ACCCAGCACT CCACTGGATA# 2200CCAAAA CAGCCTTGTG GTCAGTGTTC ATCTGCTGAC# 2250TTTTTT GGGGTTACAG TTTGAGCAGG ATATTTGGTC# 2300CACACC CTGCAGCTCC AAAGGTTCCC CACCAACAGC# 2350TTGACC CTTGAATGGG TTTTCCAGCA CCATTTTCAT# 2400CCTGAA TGCAAGTTTA ACATAGCAGT TACCCCAATA# 2450AGTAAC AGCTTCCCAC ATCAAAATAT TTCCACAGGT# 2500AATTAG GCAAAGGAAT TCCTCGACCT GCAGCCCAAG# 2550CAGAAA TCCGCGCGGT GGTTTTTGGG GGTCGGGGGT# 2600GACGCC CGGTGTTCGT GTCGCGCCAG TACATGCGGT# 2650TCCAAA AACCATGGGT CTGTCTGCTC AGTCCAGTCG# 2700CGCAAC GCCCAAAAGA ATAACCCCCA CGAACCATAA# 2750GGGACC CCGTCCCTAA CCCACGGGGC CCGTGGCTAT# 2800CCCGAC GTTGGCTGCG AGCCCTGGGC CTTCACCCGA# 2850GTGGGG AAAAGGAAGA AACGCGGGCG TATTGGCCCC# 2900GGGGTA TCGACAGAGT GCCAGCCCTG GGACCGAACC# 2950AAACGA CCCAACACCC GTGCGTTTTA TTCTGTCTTT# 3000GCGCGG GTTCCTTCCG GTATTGTCTC CTTCCGTGTT# 3050CCATCT CCCGATCCCC ACGAGTGCTG GGGCGTCGGT# 3100AGTACT TCTACACAGC CATCGGTCCA GACGGCCGCG# 3150TTGTGT ACGCCCGACA GTCCCGGCTC CGGATCGGAC# 3200GACCCT GCGCCCAAGC TGCATCATCG AAATTGCCGT# 3250TAGAGT TGGTCAAGAC CAATGCGGAG CATATACGCC# 3300TCCTGC AAGCTCCGGA TGCCTCCGCT CGAAGTAGCG# 3350TACAAG CCAACCACGG CCTCCAGAAG AAGATGTTGG# 3400GAATCC CCGAACATCG CCTCGCTCCA GTCAATGACC# 3450ATTGTC CGTCAGGACA TTGTTGGAGC CGAAATCCGC# 3500GGACTT CGGGGCAGTC CTCGGCCCAA AGCATCAGCT# 3550GCGACG GACGCACTGA CGGTGTCGTC CATCACAGTT# 3600ATGGGG ATCAGCAATC GCGCATATGA AATCACGCCA# 3650CGATTC CTTGCGGTCC GAATGGGCCG AACCCGCTCG# 3700GCCGCA GCGATCGCAT CCATGGCCTC CGCGACCGGC# 3750CAGTTC GGTTTCAGGC AGGTCTTGCA ACGTGACACC# 3800AGATGC AATAGGTCAG GCTCTCGCTG AATTCCCCAA# 3850GGAATC GGGAGCGCGG CCGATGCAAA GTGCCGATAA# 3900GTAGAA ACCATCGGCG CAGCTATTTA CCCGCAGGAC# 3950CTACAT CGAAGCTGAA AGCACGAGAT TCTTCGCCCT# 4000AGGTCG GAGACGCTGT CGAACTTTTC GATCAGAAAC# 4050CGCGGT GAGTTCAGGC TTTTTCATAT CAAGCTGATC# 4100TGACGC TGTTAAGCGG GTCGCTGCAG GGTCGCTCGG# 4150CGCGTC ACCTTAATAT GCGAAGTGGA CCTGGGACCG# 4200CATCTG CGTGTTCGAA TTCGCCAATG ACAAGACGCT# 4250TCATCA TAGAACTAAA GACATGCAAA TATATTTCTT# 4300AGCAAA CGCGAGCAAC GGGCCACGGG GATGAAGCAG# 4350GCTAAC GGATTCACCA CTCCAAGAAT TGGAGCCAAT# 4400AACTGT GAATGCGCAA ACCAACCCTT GGCAGAACAT# 4450CCATCT CCAGCAGCCG CACGCGGCGC ATCTCGGGGC# 4500ACGTCT TGCTGGCGTT CGCGACGCGA GGCTGGATGG# 4550ATTCTT CTCGCTTCCG GCGGCATCGG GATGCCCGCG# 4600GTCCAG GCAGGTAGAT GACGACCATC AGGGACAGCT# 4650CGGCTC TTACCAGCGC CAGCAAAAGG CCAGGAACCG# 4700TGCTGG CGTTTTTCCA TAGGCTCCGC CCCCCTGACG# 4750CGACGC TCAAGTCAGA GGTGGCGAAA CCCGACAGGA# 4800GGCGTT TCCCCCTGGA AGCTCCCTCG TGCGCTCTCC# 4850CGCTTA CCGGATACCT GTCCGCCTTT CTCCCTTCGG# 4900TCTCAT AGCTCACGCT GTAGGTATCT CAGTTCGGTG# 4950CAAGCT GGGCTGTGTG CACGAACCCC CCGTTCAGCC# 5000TATCCG GTAACTATCG TCTTGAGTCC AACCCGGTAA# 5050CCACTG GCAGCAGCCA CTGGTAACAG GATTAGCAGA# 5100CGGTGC TACAGAGTTC TTGAAGTGGT GGCCTAACTA# 5150GGACAG TATTTGGTAT CTGCGCTCTG CTGAAGCCAG# 5200AGAGTT GGTAGCTCTT GATCCGGCAA ACAAACCACC# 5250TTTTTT TGTTTGCAAG CAGCAGATTA CGCGCAGAAA# 5300AAGATC CTTTGATCTT TTCTACGGGG TCTGACGCTC# 5350TCACGT TAAGGGATTT TGGTCATGAG ATTATCAAAA# 5400GATCCT TTTAAATTAA AAATGAAGTT TTAAATCAAT# 5450AGTAAA CTTGGTCTGA CAGTTACCAA TGCTTAATCA# 5500TCAGCG ATCTGTCTAT TTCGTTCATC CATAGTTGCC# 5550GTAGAT AACTACGATA CGGGAGGGCT TACCATCTGG# 5600TGATAC CGCGAGACCC ACGCTCACCG GCTCCAGATT# 5650CAGCCA GCCGGAAGGG CCGAGCGCAG AAGTGGTCCT# 5700CTCCAT CCAGTCTATT AATTGTTGCC GGGAAGCTAG# 5750CAGTTA ATAGTTTGCG CAACGTTGTT GCCATTGCTG# 5800TCACGC TCGTCGTTTG GTATGGCTTC ATTCAGCTCC# 5850AAGGCG AGTTACATGA TCCCCCATGT TGTGCAAAAA# 5900TCGGTC CTCCGATCGT TGTCAGAAGT AAGTTGGCCG# 5950ATGGTT ATGGCAGCAC TGCATAATTC TCTTACTGTC# 6000ATGCTT TTCTGTGACT GGTGAGTACT CAACCAAGTC# 6050GTATGC GGCGACCGAG TTGCTCTTGC CCGGCGTCAA# 6100GCGCCA CATAGCAGAA CTTTAAAAGT GCTCATCATT# 6150GGGGCG AAAACTCTCA AGGATCTTAC CGCTGTTGAG# 6200AACCCA CTCGTGCACC CAACTGATCT TCAGCATCTT# 6250GTTTCT GGGTGAGCAA AAACAGGAAG GCAAAATGCC# 6300AAGGGC GACACGGAAA TGTTGAATAC TCATACTCTT# 6350ATTGAA GCATTTATCA GGGTTATTGT CTCATGAGCG# 6400TGTATT TAGAAAAATA AACAAATAGG GGTTCCGCGC# 6450AGTGCC ACCTGACGTC TAAGAAACCA TTATTATCAT# 6500AAAATA GGCGTATCAC GAGGCCCTTT CGTCTTCAAG# 6550ACAGCT TATCGTAGAC ATCATGCGTG CTGTTGGTGT# 6600GTCTTG TCACCATTTT CGTCCTCCCA ACATGGGGCA# 6650TGTTGT CACGTCACTC AGCTCCGCGC TCAACACCTT# 6700CATTAG CGACATTTAC CTGGTGAGCA ATCAGACATG# 6750TGGCCT CCTTAAATTC ACCTAAGAAT GGGAGCAACC# 6800AAGCAG CGAAAATTCA CGCCCCCTTG GGAGGTGGCG# 6850TAGCAC TCCCACTCTA CTACTGGGTA TCATATGCTG# 6900AGGATA GCATATGCTA CCCGGATACA GATTAGGATA# 6950GATATA GATTAGGATA GCATATGCTA CCCAGATATA# 7000ATGCTA CCCAGATATA AATTAGGATA GCATATACTA# 7050AGGATA GCATATGCTA CCCAGATATA GATTAGGATA# 7100GATATA GATTAGGATA GCATATGCTA CCCAGATATA# 7150ATGCTA TCCAGATATT TGGGTAGTAT ATGCTACCCA# 7200TAGCAT ATACTACCCT AATCTCTATT AGGATAGCAT# 7250CAGATT AGGATAGCAT ATACTACCCA GATATAGATT# 7300TACCCA GATATAGATT AGGATAGCCT ATGCTACCCA# 7350TAGCAT ATACTACCCA GATATAGATT AGGATAGCAT# 7400TAGATT AGGATAGCCT ATGCTACCCA GATATAGATT# 7450TATCCA GATATTTGGG TAGTATATGC TACCCATGGC# 7500GTGCTC TCAGCGACCT CGTGAATATG AGGACCAACA# 7550GCTCAG GCGCAAGTGT GTGTAATTTG TCCTCCAGAT# 7600CCCTAT CTTGGCCCGC CCACCTACTT ATGCAGGTAT# 7650TTAGTG GTTTTGTGGG CAAGTGGTTT GACCGCAGTG# 7700AATCAG CCAAGTTATT ACACCCTTAT TTTACAGTCC# 7750GCGTGT GGGGGCTGAC GCGTGCCCCC ACTCCACAAT# 7800TGGCCA CTTGTCTTTG TTTATGGGCC CCATTGGCGT# 7850TTTTCG GGGGTGTTAG AGACAACCAG TGGAGTCCGC# 7900ACTCTC TTTCCCCTTG TTACAAATAG AGTGTAACAA# 7950CTTGGT CCCTGCCTGG GACACATCTT AATAACCCCA# 8000TAGGAT TATGTGTTGC CCATAGCCAT AAATTCGTGT# 8050GTCTTT ACGGCTTGTC CCCACCCCAT GGATTTCTAT# 8100AGAATG TTTCATTCCT ACACTAGTAT TTATTGCCCA# 8150GTTATA TTGGTGTCAT AGCACAATGC CACCACTGAA# 8200TTTATT CTGGGGGCGT CACCTGAAAC CTTGTTTTCG# 8250ACCTTA CTGTTCACAA CTCAGCAGTT ATTCTATTAG# 8300ATGAAG AAGCAGGCGA AGATTCAGGA GAGTTCACTG# 8350TTCAGC CACTGCCCTT GTGACTAAAA TGGTTCACTA# 8400TGACCC CATGTAAATA AAACCGTGAC AGCTCATGGG# 8450TGTTCC TTAGGACCCT TTTACTAACC CTAATTCGAT# 8500GTTGGG TAACATATGC TATTGAATTA GGGTTAGTCT# 8550ACTACC CGGGAAGCAT ATGCTACCCG TTTAGGGTTA# 8600TAAACA CTATTGCTAA TGCCCTCTTG AGGGTCCGCT# 8650CAGGCC CCTCTGATTG ACGTTGGTGT AGCCTCCCGT# 8700CCTGGG AGGTACATGT CCCCCAGCAT TGGTGTAAGA# 8750TTACAC ATAAAGGCAA TGTTGTGTTG CAGTCCACAG# 8800TCCAGG ATGAAAGCCA CTCAGTGTTG GCAAATGTGC# 8850GGATGT CAACTACAGT CAGAGAACCC CTTTGTGTTT# 8900TCACAT GTGGAACAGG GCCCAGTTGG CAAGTTGTAC# 8932 TTAC ATGCACTGCC CC- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 484 ami - #no acids (B) TYPE: amino aci - #d (C) STRANDEDNESS: Sing - #le (D) TOPOLOGY: Linear- (ii) MOLECULE TYPE: cDNA to mRNA (A) DESCRIPTION: predi - #cted amino acid sequence of Porcine E - #-selectin- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #9:- Met Ile Ala Ser Gln20- Phe Leu Ser Ala Leu Pro Leu Val Leu Leu Le - #u Leu Arg Glu5- Ser Gly Ala Trp Ser Tyr Ser Ala Ser Thr Gl - #u Thr Met Thr# 10- Phe Asp Asp Ala Ser Ala Tyr Cys Gln Gln Ar - #g Tyr Thr His# 25- Leu Val Ala Ile Gln Asn His Ala Glu Ile Gl - #u Tyr Leu Asn# 35- Ser Thr Phe Asn Tyr Ser Ala Ser Tyr Tyr Tr - #p Ile Gly Ile#50- Arg Lys Ile Asn Gly Thr Trp Thr Trp Ile Gl - #y Thr Lys Lys# 65- Ala Leu Thr Pro Glu Ala Thr Asn Trp Ala Pr - #o Gly Glu Pro# 80- Asn Asn Lys Gln Ser Asn Glu Asp Cys Val Gl - #u Ile Tyr Ile# 95- Lys Arg Asp Lys Asp Ser Gly Lys Trp Asn As - #p Glu Arg Cys# 105- Ser Lys Lys Lys Leu Ala Leu Cys Tyr Thr Al - #a Ala Cys Thr110 1 - #15 1 - #20- Pro Thr Ser Cys Ser Gly His Gly Glu Cys Il - #e Glu Thr Ile# 135- Asn Ser Ser Thr Cys Gln Cys Tyr Pro Gly Ph - #e Arg Gly Leu# 150- Gln Cys Glu Gln Val Val Glu Cys Asp Ala Le - #u Glu Asn Pro# 165- Val Asn Gly Val Val Thr Cys Pro Gln Ser Le - #u Pro Trp Asn# 175- Thr Thr Cys Ala Phe Glu Cys Lys Glu Gly Ph - #e Glu Leu Ile180 1 - #85 1 - #90- Gly Pro Glu His Leu Gln Cys Thr Ser Ser Gl - #y Ser Trp Asp# 205- Gly Lys Lys Pro Thr Cys Lys Ala Val Thr Cy - #s Asp Thr Val# 220- Gly His Pro Gln Asn Gly Asp Val Ser Cys As - #n His Ser Ser# 235- Ile Gly Glu Phe Ala Tyr Lys Ser Thr Cys Hi - #s Phe Thr Cys# 245- Ala Glu Gly Phe Gly Leu Gln Gly Pro Ala Gl - #n Ile Glu Cys250 2 - #55 2 - #60- Thr Ala Gln Gly Gln Trp Thr Gln Gln Ala Pr - #o Val Cys Lys# 275- Ala Val Lys Cys Pro Ala Val Ser Gln Pro Ly - #s Asn Gly Leu# 290- Val Lys Phe Thr His Ser Pro Thr Gly Glu Ph - #e Thr Tyr Lys# 305- Ser Ser Cys Ala Phe Ser Cys Glu Glu Gly Ph - #e Glu Leu Arg# 315- Gly Ser Ala Gln Leu Ala Cys Thr Ser Gln Gl - #y Gln Trp Thr320 3 - #25 3 - #30- Gln Glu Val Pro Ser Cys Gln Val Val Gln Cy - #s Ser Ser Leu# 345- Glu Val Pro Arg Glu Ile Asn Met Ser Cys Se - #r Gly Glu Pro# 360- Val Phe Gly Ala Val Cys Thr Phe Ala Cys Pr - #o Glu Gly Trp# 375- Met Leu Asn Gly Ser Val Ala Leu Thr Cys Gl - #y Ala Thr Gly# 385- His Trp Ser Gly Met Leu Pro Thr Cys Glu Al - #a Pro Ala Glu390 3 - #95 4 - #00- Ser Lys Ile Pro Leu Ala Met Gly Leu Ala Al - #a Gly Gly Val# 415- Ser Phe Met Thr Ser Ala Ser Phe Leu Leu Tr - #p Leu Leu Lys# 430- Arg Leu Arg Lys Arg Ala Lys Lys Phe Val Pr - #o Ser Ser Ser# 445- Ser Glu Cys Leu Gln Pro Asn Gly Ser Tyr Gl - #n Met Pro Ser# 455- Asp Leu Ile460__________________________________________________________________________

Claims

1. An isolated porcine E-selectin produced by a method comprising growing a recombinant host cell containing an isolated nucleic acid molecule comprising:

(a) a nucleic acid molecule encoding amino acid 1 through amino acid 405 of SEQ ID NO:9; or

(b) a nucleic acid molecule encoding amino acid 1 through amino acid 462 of SEQ ID NO:9,

such that the protein encoded by the nucleic acid molecule is expressed by the host cell, and isolating the expressed porcine E-selectin.

2. Isolated porcine E-selectin having the amino acid sequence of SEQ ID NO:9 from amino acid 1 through amino acid 462.

3. Isolated soluble porcine E-selectin comprising the amino acid sequence of SEQ ID NO:9 from amino acid 1 through amino acid 405.