Patent Application
20160002310
This application claims priority to PCT application PCT/CA2014/050104 filed on Feb. 14, 2104 which claims priority to U.S. provisional patent application No. 61/765,203, filed on Feb. 15, 2013,the contents of which are expressly incorporated by reference.
This invention relates to INGAP peptides with islet β-cell neogenic or regenerative activity, and compositions and methods thereof for the treatment and prevention of diabetes.
Diabetes mellitus affects over 100 million individuals worldwide. In the U.S., the estimated healthcare costs of those affected by diabetes is approximately 136 billion dollars annually. Diabetes mellitus is a disorder of the metabolism that is characterized by the inability of the pancreas to secrete sufficient amounts of insulin, which results in large fluctuations in blood glucose levels and can have both short- and long-term physiological consequences. Long-term complications arising from elevated blood glucose levels (hyperglycemia) in patients with Type 1 diabetes (insulin-dependent diabetes mellitus, or IDDM) include retinopathy, neuropathy, nephropathy and other vascular complications. Low glucose levels (hypoglycemia) can lead to diabetic coma, seizures, accidents, anoxia, brain damage, decreased cognitive function, and death.
Type 2 diabetes, also known as non-insulin dependent diabetes mellitus or NIDDM, is a progressive disease characterized by impaired glucose metabolism resulting in elevated blood glucose levels. Patients with Type 2 diabetes exhibit impaired pancreatic beta-cell function resulting in failure of the pancreatic beta-cells to secrete an appropriate amount of insulin in response to a hyperglycemic signal, and resistance to the action of insulin at its target tissues (insulin resistance).
Current treatments of Type 2 diabetes aim to reverse insulin resistance, control intestinal glucose absorption, normalize hepatic glucose production, and improve beta-cell glucose sensing and insulin secretion. Because of the shortcomings of current treatments for diabetes, new treatments for Type 1 and Type 2 diabetes, as well as new diagnostic and prognostic methods, are highly desirable.
Increasing evidence indicates that inadequate β-cell mass underlies Type 1 and Type 2 diabetes. Therefore, regeneration of β-cells in diabetic patients is an important goal of diabetes research. In recent years, there has been increasing interest in the development of new strategies to induce β-cell regeneration and new islet formation in situ (Baggio, L. L. and Drucker, D. J., 2006, Annu Rev Med, 57:265-281). Identification of bioactive molecules with the capacity to stimulate expansion of the remaining β-cell mass or with islet neogenic activity is therefore crucial for harnessing the regenerative potential of the native pancreas.
Islet Neogenesis Associated Protein (INGAP) is a 16.8 kDa protein originally identified in a crude extract from a partially obstructed hamster pancreas (Rosenberg, L., et al., 1988, Diabetes, 37: 334-341; U.S. Pat. No. 5,834,590). INGAP is expressed in the pancreas and duodenum and has been shown to induce islet neogenesis in several species (Rosenberg, L., et al., 1996, Diabetologia, 39: 256-262; Rosenberg, L., et al., 2004, Ann Surg 240: 875-884). Structurally, INGAP is a member of the Reg family of secreted C-type lectins that comprises more than 25 members, classified into 4 subfamilies based on the primary sequence (Zhang, Y. W., et al., 2003, World J Gastroenterol, 9: 2635-2641; Okamoto, H., 1999, J Hepatobiliary Pancreat Surg 6: 254-262).
INGAP belongs to the large Reg 3 subfamily that has been identified in predominantly gastrointestinal tissues (pancreas, stomach, liver) in rat, mouse, hamster and humans (Rafaeloff, R., et al., 1997, J Clin Invest 99: 2100-2109). Despite the ubiquity of Reg proteins, not much is known about their functions or mechanisms of action. While Reg 1 is believed to be a β-cell mitogen, much less is known about the functions of the Reg 3 family.
A number of studies suggest that Regs may bind specific cell-surface receptors and activate multiple signaling pathways. One argument in favor of this receptor hypothesis is that biological activity of INGAP appears to be mediated by a 15 amino acid fragment of the protein (amino acids 104-118), namely INGAP peptide (INGAP-P), which consists of a highly conserved IGLHDP motif and a unique sequence SHGTLPNGS not found in other members of the Reg family (Rafaeloff, R., et al., 1997, J Clin Invest 99: 2100-2109). Synthetic INGAP peptide has been demonstrated to be as effective as the protein in inducing new islet formation and reversing streptozotocin-induced diabetes in hamsters and mice (Rosenberg, L., et al., 1996, Diabetologia, 39: 256-262; Rosenberg, L., et al., 2004, Ann Surg 240: 875-884) and is, therefore, a possible ligand for the receptor. Biological effects of a synthetic INGAP-P have been extensively studied both in vitro and in vivo. To date, it has been shown that INGAP-P: 1) induces in vitro regeneration of functional human islets from dedifferentiated, islet-derived duct-like structures (Jamal, A. M., et al., 2005,Cell Death Differ, 12: 702-712); 2) dose dependently stimulates expansion of β-cell mass in rodents, dogs and cynomolgus monkeys (Lipsett, M., et al., 2007,Cell Biochem Biophys, 48: 127-137; Pittenger, G. L., et al., 2007, Pancreas, 34: 103-111); and 3) increases insulin secretion and β-cell size and upregulates expression of several genes related to β-cell function in rat neonatal islets in vitro (Barbosa, H., et al., 2006, Regul Pept, 136: 78-84; Borelli, M. I., et al., 2005, Regul Pept, 131: 97-102). These important results were followed by clinical trials to investigate its efficacy and safety in humans, in which INGAP-P was found to have a signal effect with an improvement of glucose homeostasis confirmed by glycosylated hemoglobin (HbA1C, or A1C) reduction at 90 days in patients with Type 2 diabetes and by a significant increase in C-peptide secretion in patients with Type 1 diabetes (Dungan, K. M., et al., 2009, Diabetes Metab Res Rev, 25: 558-565).
Despite these data which suggest that INGAP-P possesses both islet-neogenic and insulinotropic activities, it is apparent from animal studies and human trials that the 15-mer of INGAP (INGAP-P) lacks stability. Accordingly, it must be administered in a very large dose to reach a required serum and tissue threshold level. Poor stability also leads to problems with, for example, drug formulation, patient acceptance of local injection site reactions, and high cost. There is a need therefore for an INGAP analogue with comparable or greater bioactivity and/or greater stability or a longer half-life in vivo, compared to INGAP-P.
Previously we identified a pancreatic protein called Islet Neogenesis Associated Protein (INGAP), which is a member of the cross species mammalian family of REG3 proteins (see
Both INGAP and INGAP-P have been shown to induce ductal cells to differentiate into islets. In a human in vitro model of islet regeneration, INGAP-P induces increased expression of the pancreatic development transcription factor, PDX-1 and concurrent formation of new islets (Jamal, A. M., et al., Cell Death Differ., 2003, 10: 987-996; Jamal, A. M., et al., Cell Death Differ., 2005, 12: 702-712). In animal models, INGAP-P induces duct cell proliferation in vitro and islet cell regeneration from cells associated with the ductal epithelium, leading to new islet formation in the normal adult mouse, hamster, and dog pancreas. In the STZ-treated C57BL/6J mouse model of diabetes, INGAP-P reversed the diabetic state (Pittenger, G. L., et al., Pancreas, 2007, 34: 103-111; Rosenberg, L., et al., Ann. Surg., 2004, 240: 875-884 (2004); Kapur, R. et al., INGAP Induces Duct Cell Proliferation In Vitro and beta Cell Formation in Normal Non Diabetic Mice, 71st ADA Meeting, San Diego, 2011). In the NOD mouse model of established (not new-onset) autoimmune T1DM, INGAP-P in combination with the immune modulator IL-12 inhibitor, lisofylline, induced remission of hyperglycemia and elimination of the need for insulin pellets (Tersey, S. A. et al., Unique Drug Combination for Reversal of Type 1 Diabetes, 68th Scientific Sessions American Diabetes Association (ed. ADA), San Fransisco, Calif., 2008; Tersey, S. A. et al., Journal of Diabetes Mellitus, 2012, in press). Histologic examination confirmed evidence of new islets.
In human trials, INGAP-P has been evaluated in Phase 1 and 2 studies of both T1DM and T2DM patients (Dungan, K. M. et al., Diabetes Metab Res Rev, 2009, 25: 558-565). Once-daily injections of INGAP-P for 3 months caused a statistically significant increase in stimulated C-peptide secretion in T1DM patients, and a trend towards increased C-peptide levels in T2DM patients. Glycosylated hemoglobin (HbA1c) decreased by −0.6% (p<0.0125) in T2DM patients and by −0.4% (p<0.06) in T1DM patients.
Despite these highly promising results, INGAP-P's relatively short plasma half-life continues to present challenges for use of INGAP-P as a therapeutic.
Accordingly, there are provided herein INGAP peptides which retain one or more biological activities of INGAP-P and are suitable for development as a therapeutic. In an embodiment, peptides of the invention have comparable or greater bioactivity and/or greater stability or a longer half-life in vivo, compared to INGAP-P.
In an embodiment, there is provided herein a peptide comprising the sequence set forth in SEQ ID NO:4 or SEQ ID NO:6.
In another embodiment, there is provided herein a peptide consisting of the sequence set forth in SEQ ID NO:4 or SEQ ID NO:6.
In some embodiments, a peptide of the invention induces pancreatic β-cell neogenesis, induces pancreatic β-cell regeneration, improves glucose homeostasis and/or reverses hyperglycemia in a subject.
Analogs, homologs, fragments or variants of peptides of the invention are also provided herein, wherein the analog, homolog, fragment or variant has a biological activity of the peptide. Analogs, homologs, fragments or variants may have at least 80%, at least 85%, at least 90%, at least 95% at least 98%, or at least 99% sequence identity to the peptide of the invention. The biological activity may be, for example, cell or receptor binding specificity of the peptide, ability to induce pancreatic β-cell neogenesis, ability to induce islet cell regeneration, ability to improve glucose homeostasis and/or ability to reverse hyperglycemia in a subject.
Nucleic acid molecules comprising a nucleic acid sequence encoding peptides of the invention or analogs, homologs, fragments or variants thereof are also provided. A nuceic acid molecule may be operably linked to an expression control sequence to form an expression vector, wherein said expression vector is propagated in a suitable cell.
Pharmaceutical compositions comprising peptides or analogs, homologs, fragments or variants thereof of the invention, and a pharmaceutically acceptable carrier or excipient, are also provided. In an embodiment, compositions are adapted for administration orally. In another embodiment, compositions are adapted for administration by injection.
In another embodiment, there is provided a method for preventing or treating a pancreatic condition or disease comprising administering a peptide or analog, homolog, fragment or variant thereof or a composition of the invention to a subject in need thereof. In an embodiment, the condition or disease is a metabolic disorder. In another embodiment, the condition or disease is a β-cell associated disorder. In a further embodiment, the condition or disease is Type 1 diabetes, Type 2 diabetes or a complication of diabetes.
In some embodiments, β-cell death by apoptosis or necrosis is prevented or inhibited in a subject by administering peptides or analogs, homologs, fragments or variants thereof, or compositions, of the invention. In other embodiments, functionality of pancreatic cells is improved or restored in a subject, plasma insulin levels are increased in a subject, number or size of pancreatic β-cells is increased in a subject, β-cell regeneration from pancreatic ductal cells is stimulated in a subject, glucose homeostasis is restored or improved in a subject, and/or hyperglycemia is reversed in a subject.
Peptides and compositions of the invention may be administered by injection, orally, intravenously, intraperitoneally, intramuscularly or subcutaneously. In an embodiment, peptides and compositions are administered orally, once-a day.
In a particular embodiment, a subject is a human.
In some embodiments, peptides of the invention are administered with a second therapeutic agent. A second therapeutic agent may be administered concomitantly with a peptide of the invention, or a second therapeutic agent and a peptide may be administered sequentially. In an embodiment, a second therapeutic agent is a therapeutic for Type 1 or Type 2 diabetes. In another embodiment, a second therapeutic agent is anakinra
Pharmaceutical compositions for treatment of pancreatic insufficiency, comprising a peptide of the invention and a pharmaceutically acceptable carrier or excipient, are also provided. In an embodiment, a peptide or composition is capable of stimulating β-cell regeneration from pancreatic ductal cells. In another embodiment, a peptide or composition has a biological activity of mammalian INGAP protein. In one embodiment, a biological activity is ability to stimulate pancreatic duct-like cells or duct-associated cells to grow and proliferate.
Nucleic acid molecules encoding peptides of the invention or analogs, homologs, fragments or variants thereof described herein are also provided. Nucleic acid molecules may, for example, be linked to an expression control sequence to form an expression vector, wherein said expression vector is propagated in a suitable cell.
In yet another embodiment, the present invention provides pharmaceutical compositions comprising peptides or analogs, homologs, fragments or variants thereof described herein and a pharmaceutically acceptable carrier or excipient.
There are also provided herein methods for preventing or treating a pancreatic condition or disease comprising administering a peptide or analog, homolog, fragment or variant thereof of the invention to a subject in need thereof. In methods provided herein, a subject may be for example a rodent, canine, pig, primate or human.
In an embodiment, a condition or disease is a metabolic disorder, for example a β-cell associated disorder. A condition or disease may be Type 1 diabetes, Type 2 diabetes or a complication of diabetes.
In other embodiments, β-cell apoptosis is prevented or inhibited in a subject; functionality of pancreatic cells is improved or restored in a subject; plasma insulin levels are increased in a subject; and/or number or size of pancreatic cells is increased in a subject. In a particular embodiment, the pancreatic cells are β-cells.
In yet another embodiment, β-cell neogenesis is stimulated and/or glucose homeostasis is improved in a subject and/or insulin is potentiated in a subject.
Particular embodiments of the present invention will now be explained by way of example and with reference to the accompanying drawings.
Plates were then placed on ice and washed with ice-cold PBS prior to cell lysis in 150 μl of Mg+ lysis buffer containing a cocktail of protease inhibitors (NEB). 10 μl of cell lysates were used for Ras-GTP ELISA and the readings were normalized by amounts of protein (DC protein assay, Biorad). Results are shown as a Fold Change relative to the 0 min time point, which is equal to 1 and is shown as a dotted horizontal line. Results are means±S.E. of at least three independent experiments (*: p<0.05, §: p<0.01, ¶: p<0.001, compared to the 0 min control). (B): Fold change in c-Raf phosphorylation, measured by Western blot/densitometry (ImageJ), as a ratio of Phospho to total cRaf and calculated relative to the 0 min time point, shown as a dotted horizontal line (=1). Results are means±S.E. of at least three independent experiments (*: p<0.05, §: p<0.01, ¶: p<0.001).
, abbreviated names of protein kinases as depicted by numbers in (A-D), respectively and the corresponding fold-changes. Only significant changes are represented; a change in OD of at least 25% was considered significant.
Other features and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples while indicating particular embodiments of the invention are given by way of illustration only. Various changes and modifications within the spirit and scope of the disclosure will become apparent to those skilled in the art from this detailed description.
Islet Neogenesis Associated Protein (INGAP) was discovered in the partially duct-obstructed hamster pancreas, as a factor inducing formation of new duct-associated islets. We have shown previously that a bio-active portion of INGAP, INGAP104-118 peptide (also referred to herein as “INGAP-P”, “15-mer” or SEQ ID NO:1), has β-cell neogenic and insulin-potentiating activities. Recent Phase 2 clinical trials have shown that INGAP-P produced improved glucose homeostasis in both Type 1 and Type 2 diabetic patients, thus supporting the potential of INGAP as a pharmacotherapy for diabetes. However, poor stability and/or a short plasma half-life have hampered the ability to develop INGAP-P as a therapeutic.
We report herein that, to improve efficacy of INGAP-P as a medicament for treatment or prevention of diabetes and to understand its mechanism of action, we searched for clues in the full-length INGAP protein (also referred to as “rINGAP” and “r-INGAP”). We cloned rINGAP and used it to investigate signaling events induced by the protein and the INGAP-P peptide in RIN-m5 F cells. RIN-m5 F cells are a rat insulinoma cell line that responds to INGAP with an increase in proliferation. The full length recombinant protein (r-INGAP) was much more stable than the 15-mer peptide (up to 5 days in cell culture) and is 6His-tagged. The data showed that rINGAP was at least a hundred times more efficient on a molar basis than INGAP-P at stimulating proliferation of rat insulinoma RIN-m5F cells and that, although they both signal via activation of a Ras-Raf-Erk pathway, upstream signaling events may differ. We also show that binding of fluorescent-labeled rINGAP is limited to the cell surface and forms patches on the cell surface in a fashion consistent with receptor binding and clustering, whereas INGAP-P is rapidly internalized. INGAP-induced Erk½ (MAPK42/44) activation is significantly reduced by pertussis-toxin (Ptx) for both rINGAP and the 15-mer, suggesting that both rINGAP and the peptide act via a G-protein coupled receptor. Thus, the data showed that rINGAP had a much greater stability (up to 5 days in cell culture) and at least 100 times higher molar efficiency in islet regeneration, both in vitro and in vivo than INGAP-P (see
Using X-ray crystallography, a 3 D reconstruction of rINGAP was generated. This reconstruction showed that the bioactive 15-mer peptide, INGAP-P, is part of a loop extending out from the core of the molecule (
We therefore designed and produced three extended analogues of INGAP-P that included the conserved amino acids either on one side of the peptide, or on both sides (see Table 1,
Structures of 19-mer peptides are shown in Table 1. To produce extended 19-mer INGAP peptides, 4 amino acids flanking the INGAP-P 15-mer peptide in the INGAP protein sequence were added to the INGAP-P 15-mer, as shown in Table 1 (flanking amino acids added to the 15-mer are underlined; see also
Biological activity of 19-mers in comparison to INGAP-P 15-mer and to rINGAP was investigated. As shown herein, INGAP102-120- induced Erk½ (MAPK42/44) activation in cultured RIN-m5 F cells was 3 times greater than that produced by INGAP104-118 and approximately double that produced by rINGAP (
Analysis of comparative peptide stability in FBS showed no advantage of INGAP-19 over INGAP-P, as both peptides degraded at a similar rate (
To explore whether efficiency of INGAP-19 could be further augmented by increasing its stability, cyclization (disulfide, head-to-tail, by addition of terminal cysteines) was chosen, as this is a widely used approach to increase peptide stability (Adessi, C. and Soto, C., Curr Med Chem, 2002, 9: 963-978). INGAP-P was similarly cyclized and the new analogs were termed INGAP-19C and INGAP-PC (“C” for cyclized).
Stabilities of INGAP-P, INGAP-PC, INGAP-19 and INGAP-19C were compared in time-course studies of in vitro incubation in FBS. Data showed that INGAP-19C appeared more stable than linear 15-mer (INGAP-P) or 19-mer (INGAP-19) peptides (
Thus, the results indicate that a 19-mer of rINGAP, INGAP102-120 (SEQ ID NO:4) and a cyclized 19-mer of rINGAP, cyclized INGAP102-120, are more bioactive than INGAP-P 15-mer. Cyclized INGAP102-120 shows greater stability than INGAP-P.
Accordingly, there is provided herein a 19-mer peptide of INGAP, INGAP102-120 (also referred to herein as “INGAP-19 ”, “19-mer”. “19-mer seq 3 ” and SEQ ID NO:4). There is also provided herein a cyclized 19-mer peptide of INGAP, INGAP102-120 (also referred to herein as “INGAP-19C” and SEQ ID NO:6). It is shown herein that 19-mer peptides possess β-cell neogenic and insulin-potentiating activities of INGAP and/or improved stability compared to INGAP-P, indicating 19-mer INGAP peptides as potential novel therapeutics for diabetes.
In an embodiment, there is provided herein an INGAP peptide comprising the sequence set forth in SEQ ID NO: 4 or SEQ ID NO:6. In another embodiment, there is provided herein an INGAP peptide consisting of the sequence set forth in SEQ ID NO: 4 or 6.Compositions and methods of use thereof are also provided.
As used herein, “β-cells” refer to the fully differentiated insulin-producing β-cells of the islets of Langerhans in the pancreas. Pancreatic β-cells are characterized by their secretion of insulin and typically by their cell surface expression of the islet amyloid polypeptide (IAPP).
It should also be understood that analogs, homologs, fragments and variants of 19-mer peptides of the invention which retain biological activities of INGAP are encompassed by peptides of the invention. In an embodiment, variants of SEQ ID NO:4 and SEQ ID NO: 6 are provided having at least 80%, at least 85%, at least 90%, at least 95%, at least 98% or at least 99% sequence identity to SEQ ID NO:4 and SEQ ID NO:6. In another embodiment, variants have at least 80%, at least 85%, at least 90%, at least 95%, at least 98% or at least 99% identity to SEQ ID NO:4 and SEQ ID NO:6 and retain typtophan residues at INGAP positions 103 and 120 (in other words, tryptophan residues at INGAP positions 103 and 120 are not removed, substituted or altered). In yet other embodiments, variants retain at least one of the tryptophan residues at positions 103 and 120 or both tryptophan residues.
Peptides and compositions of the invention can be used for treating or preventing conditions or diseases of the pancreas. Non-limiting examples of such conditions or diseases include metabolic disorders, or conditions such as Type 1 and Type 2 diabetes mellitus, complications of diabetes (such as e.g. retinopathy, nephropathy or neuropathies, diabetic foot, ulcers, macroangiopathies), metabolic acidosis or ketosis, reactive hypoglycaemia, hyperinsulinaemia, glucose metabolic disorder, insulin resistance, metabolic syndrome, dyslipidaemias of different origins, atherosclerosis and related diseases, obesity, high blood pressure, chronic heart failure, edema and hyperuricaemia.
Expansion of β-cell mass can involve several processes, including proliferation of existing islet cells, neogenesis from duct-associated precursors or regeneration of islet cells from dedifferentiated endocrine cells. We show herein that INGAP-P induces: (1) proliferation and endocrine differentiation of normal human pancreatic duct cells (HPDE) (
Accordingly, in an embodiment peptides and compositions of the invention promote, enhance or induce β-cell neogenesis. For example, peptides and compositions of the invention improve or restore functionality of pancreatic cells, and/or may increase the number or size of pancreatic β-cells. In another embodiment, peptides and compositions of the invention promote, enhance or induce regeneration of pancreatic β-cells. In another embodiment, peptides and compositions of the invention promote, enhance or induce proliferation of pancreatic β-cells. In yet another embodiment, peptides and compositions of the invention have insulin-potentiating activities. In a further embodiment, peptides and compositions of the invention improve glucose homeostasis in a subject having Type 1 or Type 2 diabetes.
As used herein, “insulin-potentiating activity” and “insulin potentiation” refer to ability to achieve a therapeutic outcome at lower doses of insulin when insulin is administered in combination with peptides or compositions of the invention, compared to administration of insulin alone. In other words, less externally provided insulin is needed to achieve a certain therapeutic outcome when insulin is administered in combination with peptides or compositions of the invention; in the presence of peptides or compositions of the invention, a similar therapeutic outcome is achieved with lower doses of insulin as with higher doses of insulin alone.
In further embodiments, peptides and compositions of the invention prevent β-cell death by, e.g., apoptosis or necrosis of pancreatic β-cells; induce differentiation of new functional islets from primitive duct-like structures (DLS) derived from dedifferentiated adult islets; enhance endocrine differentiation; induce islet cell regeneration from cells associated with ductal epithelium, leading to new islet formation; and/or lead to reversal of hyperglycemia. In a particular embodiment, peptides and compositions of the invention induce differentiation of pancreatic duct cells, and/or allow such cells to avoid apoptotic pathways.
In still further embodiments, peptides of the invention have better in vitro stability, greater stability in the circulation and/or a longer half-life in vivo compared to INGAP-P 15-mer peptide.
In an embodiment, a β-cell associated disorder is treated or prevented by peptides and compositions of the invention. In a particular embodiment, diabetes, particularly Type 1 diabetes, Type 2 diabetes, preclinical Type 1 diabetes, and/or diabetic complications are treated or prevented by peptides and compositions of the invention.
Thus, in one aspect there is provided herein a method for treating or preventing a metabolic disorder in a subject in need thereof, comprising administering a therapeutically-effective amount of a peptide or composition of the invention to the subject. In another aspect, there is provided a method for treating or preventing diabetes in a subject in need thereof, comprising administering a therapeutically-effective amount of a peptide or composition of the invention, e.g. SEQ ID NO:4, to the subject.
In yet another aspect, there is provided a method for preventing degeneration of pancreatic β-cells and/or for improving and/or restoring functionality of pancreatic β-cells in a subject in need thereof, comprising administering a therapeutically-effective amount of a peptide or composition of the invention to the subject. In one aspect, the number or size of pancreatic cells, e.g. β-cells, is increased in the subject, and/or plasma insulin levels are increased in the subject, and/or glucose homeostasis is restored or improved in the subject.
In a further aspect, there is provided a method of protecting islet cells against diabetogenic agents in vitro and/or in vivo, comprising contacting an eukaryotic cell with, or administering to a subject, a peptide or composition of the invention. In an embodiment, islet viability is improved, and/or islet dysfunction is blocked, and/or β-cell mass is preserved in a subject after administration of a peptide or composition of the invention.
According to another embodiment of the invention, a method of inducing differentiation of β-cell progenitors is provided, comprising: contacting a culture of pancreatic duct cells comprising β-cell progenitors with a preparation of a peptide of the invention, to induce differentiation of said β-cell progenitors. In an embodiment, pancreatic duct cells of a mammal with pancreatic endocrine failure can be removed from the body and treated in vitro. Duct cells typically comprise β-cell progenitors. Thus treatment with a preparation of a peptide of the invention will induce differentiation of the β-cell progenitors. Cells treated with peptides of the invention can then be used as an autologous transplant into the mammal from which they were derived. Such an autologous treatment minimizes adverse host versus graft reactions involved in transplants.
In one embodiment, the subject can be a rodent, a canine, a pig, a primate or a human. Although methods of the present invention can be used in any mammal, the subject is preferably a human.
The term “homolog” is used to mean those amino acid or nucleic acid sequences which have slight or inconsequential sequence variations from the sequences of the peptides described herein, such that homolog sequences function in substantially the same manner as the original sequences. Sequence variations may be attributable to local mutations or structural modifications. Sequences having substantial sequence identity include nucleic acid sequences having at least 80%, at least 85%, at least 90%, at least 95%, at least 98% or at least 99% sequence identity to sequences that encode peptides as provided herein, or amino acid sequences having at least 80%, at least 85%, at least 90%, at least 95%, at least 98% or at least 99% sequence identity to peptides provide herein (such as SEQ ID NO: 4 or SEQ ID NO:6). Sequence identity can be calculated according to methods known in the art. Nucleic acid sequence identity is most preferably assessed by the algorithm of BLAST version 2.1 advanced search. A series of programs is available at http://www.ncbi.nlm.nih.gov/BLAST.
The term “analog” is used to mean an amino acid or nucleic acid sequence which has been modified as compared to the sequence of the peptides described herein, wherein the modification does not alter biological activity of the sequence (e.g., induction of pancreatic β-cell neogenesis, induction of pancreatic β-cell regeneration, improvement of glucose homeostasis, or reversal of hyperglycemia) as described herein. Modified sequences or analogs may have improved properties over peptides described herein, e.g., SEQ ID NO:4 or SEQ ID NO:6.
Also encompassed are sequences that hybridize to the complement of a nucleotide sequence encoding a peptide of the invention, and that hybridize to the complement of a nucleotide sequence encoding a peptide which maintains a biological activity of SEQ ID NO:4 or SEQ ID NO:6, e.g., β-cell neogenesis activity, in vivo stability, etc. The term “sequence that hybridizes” means a nucleic acid sequence that can hybridize to a sequence under stringent hybridization conditions. Appropriate “stringent hybridization conditions” which promote DNA hybridization are known to those skilled in the art, and may be found for example in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1 -6.3.6. The term “stringent hybridization conditions” as used herein means that conditions are selected which promote selective hybridization between two complementary nucleic acid molecules in solution. Hybridization may occur to all or a portion of a nucleic acid sequence molecule. The hybridizing portion is at least 50% the length with respect to one of the polynucleotide sequences encoding a polypeptide. In this regard, the stability of a nucleic acid duplex, or hybrids, is determined by the Tm, which in sodium containing buffers is a function of the sodium ion concentration, G/C content of labeled nucleic acid, length of nucleic acid probe (1), and temperature (Tm=81.5° C.-16.6 (Log10 [Na+])+0.41 (%(G+C)−600/1). Accordingly, the parameters in the wash conditions that determine hybrid stability are sodium ion concentration and temperature. In order to identify molecules that are similar, but not identical, to a known nucleic acid molecule a 1% mismatch may be assumed to result in about a 1° C. decrease in Tm, for example if nucleic acid molecules are sought that have a greater than 95% identity, the final wash will be reduced by 5° C. Based on these considerations, in one embodiment stringent hybridization conditions are defined as: hybridization at 5×sodium chloride/sodium citrate (SSC)/5 × Denhardt's solution/1.0% SDS at Tm (based on the above equation) −5° C., followed by a wash of 0.2×SSC/0.1% SDS at 60° C.
Peptides may be modified to contain amino acid substitutions, insertions and/or deletions that do not alter biological activity of the peptide. Conservative amino acid substitutions involve replacing one or more amino acids of a peptide with amino acids of similar charge, size, and/or hydrophobicity characteristics. When only conservative substitutions are made, it is expected that a resulting analog would be functionally equivalent to an unsubstituted peptide. Non-conservative substitutions involve replacing one or more amino acids of a peptide with one or more amino acids which possess dissimilar charge, size, and/or hydrophobicity characteristics.
A peptide may be modified to make it more therapeutically effective or suitable, e.g., stable. For example, a peptide of the present invention may be converted into a pharmaceutically-acceptable salt by reacting with inorganic acids such as, for example, hydrochloric acid, sulphuric acid, hydrobromic acid, phosphoric acid, etc., or organic acids such as formic acid, acetic acid, propionic acid, glycolic acid, lactic acid, pyruvic acid, oxalic acid, succinic acid, malic acid, tartaric acid, citric acid, benzoic acid, salicylic acid, benzenesulphonic acid, and tolunesulphonic acids, for example. Pharmaceutically-acceptable salts are well-known in the art and pharmaceutically-acceptable salts of peptides and analogs, homologs, fragments and variants thereof are encompassed herein.
Additionally, peptides may be chemically modified by covalent conjugation to a polymer to increase its circulating half-life, for example. Exemplary polymers, and methods to attach them to peptides, are shown in U.S. Pat. Nos. 4,766,106, 4,179,337, 4,495,285, and 4,609,546. Non-limiting examples of polymers are polyoxyethylated polyols and polyethylene glycol (PEG). PEG is soluble in water at room temperature and has the general formula: R(O—CH2—CH2)nO—R where R can be hydrogen, or a protective group such as an alkyl or alkanol group. In an embodiment, the protective group has between 1 and 8 carbons, or is methyl. The symbol n is a positive integer, for example between 1 and 1,000, or between 2 and 500. In an embodiment, the PEG has an average molecular weight between 1000 and 40,000, between 2000 and 20,000, or between 3,000 and 12,000. PEG may have at least one hydroxy group, or a terminal hydroxy group. This hydroxy group may be activated to react with a free amino group on the inhibitor.
The present invention also provides expression vectors comprising a nucleic acid sequence encoding a peptide of the invention or a fragment or analog thereof
Possible expression vectors include, but are not limited to, cosmids, plasmids, artificial chromosomes, viral vectors or modified viruses (e.g. replication defective retroviruses, adenoviruses and adeno-associated viruses), so long as the vector is compatible with the host cell used. The expression vectors are “suitable for transformation of a host cell”, which means that the expression vectors contain a nucleic acid molecule of the invention and regulatory sequences selected on the basis of the host cells to be used for expression, operatively linked to the nucleic acid molecule of the invention. “Operatively linked” is intended to mean that the nucleic acid is linked to regulatory sequences in a manner which allows expression of the nucleic acid.
There is provided herein a recombinant expression vector containing a nucleic acid molecule of the invention, or a fragment or analog thereof, and necessary regulatory sequences for transcription and translation of the inserted peptide-encoding sequence.
Suitable regulatory sequences may be derived from a variety of sources, including bacterial, fungal, viral, mammalian, or insect genes (for example, see the regulatory sequences described in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990). Selection of appropriate regulatory sequences is dependent on the host cell, and may be readily accomplished by one of ordinary skill in the art. Examples of such regulatory sequences include: a transcriptional promoter and enhancer or RNA polymerase binding sequence, a ribosomal binding sequence, including a translation initiation signal. Additionally, depending on the host cell chosen and the vector employed, other sequences, such as an origin of replication, additional DNA restriction sites, enhancers, and sequences conferring inducibility of transcription may be incorporated into the expression vector.
Recombinant expression vectors of the invention may also contain a selectable marker gene which facilitates selection of host cells transformed or transfected with a peptide of the disclosure. Examples of selectable marker genes are genes encoding a protein such as G418 and hygromycin which confer resistance to certain drugs, β-galactosidase, chloramphenicol acetyltransferase, firefly luciferase, or an immunoglobulin or portion thereof such as the Fc portion of an immunoglobulin, such as IgG. Transcription of a selectable marker gene is monitored by changes in concentration of the selectable marker protein such as β-galactosidase, chloramphenicol acetyltransferase, or firefly luciferase. If a selectable marker gene encodes a protein conferring antibiotic resistance such as neomycin resistance, transformant cells can be selected with G418.Cells that have incorporated a selectable marker gene will survive, while other cells die. This makes it possible to visualize and assay for expression of recombinant expression vectors of the disclosure and in particular to determine the effect of a mutation on expression and phenotype. It will be appreciated that selectable markers can be introduced on a separate vector from the nucleic acid of interest.
Recombinant expression vectors provided herein may also contain genes which encode a moiety which provides increased expression of a peptide; increased solubility of a recombinant peptide; and/or aid in purification of a target recombinant peptide by acting as a ligand in affinity purification. For example, a proteolytic cleavage site may be added to a target recombinant peptide to allow separation of a recombinant protein from a fusion moiety subsequent to purification of a fusion protein. Typical fusion expression vectors include pGEX (Amrad Corp., Melbourne, Australia), pMal (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to a recombinant peptide.
Recombinant expression vectors can be introduced into host cells to produce a transformed host cell. The term “transformed host cell” is intended to include cells that are capable of being transformed or transfected with a recombinant expression vector of the invention. The terms “transduced”, “transformed with”, “transfected with”, “transformation” and “transfection” are intended to encompass introduction of nucleic acid (e.g. a vector or naked RNA or DNA) into a cell by one of many possible techniques known in the art. Prokaryotic cells can be transformed with nucleic acid by, for example, electroporation or calcium-chloride mediated transformation. For example, nucleic acid can be introduced into mammalian cells via conventional techniques such as calcium phosphate or calcium chloride co-precipitation, DEAE-dextran mediated transfection, lipofectin, electroporation, microinjection, RNA transfer, DNA transfer, artificial chromosomes, viral vectors and any emerging gene transfer technologies. Suitable methods for transforming and transfecting host cells can be found in Sambrook et al. (Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring Harbor Laboratory press (1989)), and other laboratory textbooks.
Suitable host cells include a wide variety of eukaryotic host cells and prokaryotic cells. For example, peptides of the disclosure may be expressed in yeast cells or mammalian cells. Other suitable host cells can be found in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1991). In addition, peptides of the disclosure may be expressed in prokaryotic cells, such as Escherichia coli (Zhang et al., Science 303 (5656): 371-3 (2004)).
Mammalian cells suitable for use in methods described herein include, among others: COS (e.g., ATCC No. CRL 1650 or 1651), BHK (e.g. ATCC No. CRL 6281), CHO (ATCC No. CCL 61), and HeLa (e.g., ATCC No. CCL 2) and 3 T3 mouse fibroblasts (e.g. ATCC No. CCL92).
Suitable expression vectors for directing expression in mammalian cells generally include a promoter (e.g., derived from viral material such as polyoma, Adenovirus 2, cytomegalovirus and Simian Virus 40), as well as other transcriptional and translational control sequences. Examples of mammalian expression vectors include without limitation pCDM8 (Seed, B., Nature 329:840 (1987)), pMT2 PC (Kaufman et al., EMBO J. 6:187-195 (1987)) and pCMV (Clontech, California, U.S.A.).
Alternatively, peptides of the invention may also be expressed in non-human transgenic animals, such as rats, mice, rabbits, sheep and pigs (Hammer et al. Nature 315:680-683 (1985); Palmiter et al. Science 222:809-814 (1983); Brinster et al. Proc. Natl. Acad. Sci. USA 82:4438-4442 (1985); Palmiter and Brinster Cell 41:343-345 (1985) and U.S. Pat. No. 4,736,866). The present invention also encompasses tissues and cells derived or isolated from such animals.
In addition to analogs and homologs described above, in certain embodiments, peptides of the invention may further be recombinantly fused to a heterologous polypeptide at the N- or C-terminus or chemically conjugated (including covalent and non-covalent conjugations) to polypeptides or other compositions. For example, peptides may be recombinantly fused or conjugated to molecules useful as labels in detection assays and effector molecules such as heterologous polypeptides, histidine (HIS) tags, drugs, radionuclides, or toxins. See, e.g., PCT publications WO 92/08495; WO 91/14438; WO 89/12624; U.S. Pat. No. 5,314,995; and EP 396,387. Any type of molecule may be covalently attached to peptides of the invention as long as it does not inhibit biological activity of the peptide. For example, but not by way of limitation, peptide derivatives include peptides that have been modified, e.g., by glycosylation, acetylation, pegylation, phosphylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, linkage to a cellular ligand or other protein, etc. Any of numerous chemical modifications may be carried out by known techniques, including, but not limited to specific chemical cleavage, acetylation, formylation, metabolic synthesis of tunicamycin, etc.
The heterologous polypeptide to which a peptide is fused may be useful for example to increase the in vivo half life of the peptide, or for use in immunoassays using methods known in the art. Peptides of the invention can be fused to marker sequences, such as a polypeptide to facilitate purification or detection. In general, it should be understood that peptides of the present invention may be used in non-conjugated form or may be conjugated to at least one of a variety of molecules, e.g., to improve therapeutic properties of the molecule, to improve pharmacokinetic properties of the molecule, etc.
In certain embodiments, a peptide of the invention includes an additional amino acid sequence or one or more moieties. Exemplary modifications are described in more detail below. For example, peptides may be modified to add an additional functional moiety (e.g., PEG, a drug, a toxin, an imaging agent or a label).
Furthermore, nucleotide or amino acid substitutions, deletions, or insertions leading to conservative substitutions or changes at “non-essential” amino acid regions may be made. For example, a peptide may be identical to the starting sequence except for one or more individual amino acid substitutions, insertions, or deletions, e.g., one, two, three, four, five, six, seven, eight, nine, or ten or more individual amino acid substitutions, insertions, or deletions may be made. In other embodiments, a peptide derived from a starting peptide may be identical to the starting sequence except for one, two or fewer, three or fewer, four or fewer, five or fewer, six or fewer, seven or fewer, eight or fewer, nine or fewer, or ten or fewer individual amino acid substitutions, insertions, or deletions. In certain embodiments, a peptide derived from a starting peptide has one, two, three, one to two, one to three, one to five or one to ten individual amino acid substitutions, insertions, or deletions relative to the starting sequence. In a particular embodiment, at least one or both of the tryptophan residues at positions 2 and 19 of SEQ ID NO:4 are retained in a derivative peptide, i.e., at least one or both of the tryptophan residues at positions 2 and 19 are retained.
Also encompassed in the present invention are fragments, derivatives, modifications, or variants of peptides described herein, as well as analogs and homologs described above, and any combination thereof. The terms “fragment,” “variant,” “derivative”, “modification”, “homolog” and “analog” when referring to peptides of the present invention include any polypeptides which retain at least some of the biological activities of the corresponding starting peptide sequences. The terms “variant,” “derivative” and “modification” are used interchangeably herein.
Variants of peptides of the present invention include fragments, polypeptides with altered amino acid sequences due to amino acid substitutions, deletions, or insertions as described herein, and modifications as described herein. Variant polypeptides may comprise conservative or non-conservative amino acid substitutions, deletions or additions as described herein. Variants may also have one or more residues chemically derivatized by reaction of a functional side group. Also included as variants are those peptides which contain one or more naturally occurring amino acid derivatives of the twenty standard amino acids. For example, 4-hydroxyproline may be substituted for proline; 5-hydroxylysine may be substituted for lysine; 3-methylhistidine may be substituted for histidine; homoserine may be substituted for serine; and ornithine may be substituted for lysine. Additionally, a variant may contain one or more non-classical amino acids.
Thus in one embodiment, analogs, homologs, fragments or variants of peptides disclosed herein are encompassed by the present invention. In an embodiment, analogs, homologs, fragments or variants retain biological activity/activities of the starting peptide, e.g., β-cell neogenesis activity, insulin potentiating activity, ability to restore or improve glucose homeostasis in a subject, ability to reverse hyperglycemia, binding to cellular receptors, stability, etc. One or more of the biological activities of a peptide may be retained by analogs, homologs, fragments or variants. In an embodiment, an analog, homolog, fragment or variant retains at least one biological activity or property of the starting peptide.
In an embodiment, peptides of the invention are purified, or substantially pure. In another embodiment, peptides of the invention are synthesized chemically.
Pharmaceutical compositions encompassing peptides of the invention are encompassed herein. Peptides of the present invention can be administered to a subject in a conventional dosage form prepared by combining a peptide of the invention with a conventional pharmaceutically acceptable carrier or diluent according to known techniques. It will be recognized by one of skill in the art that the form and character of the pharmaceutically acceptable carrier or diluent is dictated by the amount of active ingredient with which it is to be combined, the route of administration and other well-known variables.
Methods of preparing and administering peptides or analogs, homologs, fragments or variants thereof to a subject are well-known in the art or are readily determined by those skilled in the art. The route of administration of peptides and compositions of the invention may be, for example, oral, parenteral, by inhalation or topical. The term parenteral as used herein includes, e.g., intravenous, intraarterial, intraperitoneal, intramuscular, subcutaneous, rectal or vaginal administration. In a particular embodiment, a peptide or composition of the invention is administered by injection. In an embodiment, the administration route is intravenous. In another embodiment, a peptide or composition of the invention is administered orally, e.g., once daily, twice daily, or three times daily.
Usually, a suitable pharmaceutical composition for injection may comprise a buffer (e.g. acetate, phosphate or citrate buffer), a surfactant (e.g. polysorbate), and optionally a stabilizer agent (e.g. human albumin), etc. Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. In the subject invention, pharmaceutically acceptable carriers include, but are not limited to, 0.01-0.1 M and preferably 0.05 M phosphate buffer or 0.8% saline. Other common parenteral vehicles include sodium phosphate solutions, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's, or fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers, such as those based on Ringer's dextrose, and the like. Preservatives and other additives may also be present such as for example, antimicrobials, antioxidants, chelating agents, and inert gases and the like.
More particularly, pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for extemporaneous preparation of sterile injectable solutions or dispersions. In such cases, a composition must be sterile and should be fluid to the extent that easy syringability exists. It should be stable under conditions of manufacture and storage and will preferably be preserved against contaminating action of microorganisms, such as bacteria and fungi. A carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof. Proper fluidity can be maintained, for example, by use of a coating such as lecithin, by maintenance of required particle size in the case of dispersion and by use of surfactants. Suitable formulations for use in therapeutic methods disclosed herein are described in Remington's Pharmaceutical Sciences, Mack Publishing Co., 16th ed. (1980).
Prevention of action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols, such as mannitol, sorbitol, or sodium chloride in a composition. Prolonged absorption of injectable compositions can be brought about by including in a composition an agent which delays absorption, for example, aluminum monostearate and gelatin.
In any case, sterile injectable solutions can be prepared by incorporating a peptide of the invention (by itself or in combination with other active agents) in a required amount in an appropriate solvent with one or a combination of ingredients, as required and easily determined by a person of skill in the art, followed by filtered sterilization. Generally, dispersions are prepared by incorporating an active compound into a sterile vehicle, which contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for preparation of sterile injectable solutions, preferred methods of preparation are vacuum drying and freeze-drying, which yields a powder of an active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof Preparations for injections are processed, filled into containers such as ampoules, bags, bottles, syringes or vials, and sealed under aseptic conditions according to methods known in the art.
After a liquid pharmaceutical composition is prepared, it may be lyophilized to prevent degradation and to preserve sterility. Methods for lyophilizing liquid compositions are known to those of ordinary skill in the art. Just prior to use, a composition may be reconstituted with a sterile diluent (Ringer's solution, distilled water, or sterile saline, for example) which may include additional ingredients. Upon reconstitution, a composition is administered to subjects using those methods that are known to those skilled in the art.
Further, preparations may be packaged and sold in the form of a kit. Such articles of manufacture will preferably have labels or package inserts providing instructions for use and may have additional components required for use of preparations.
Those skilled in the art will appreciate that effective doses of peptides and compositions of the present invention, e.g. for preventing or treating diabetes, vary depending upon many different factors, including means of administration, characteristics or physiological state of the subject (such as state of health), other medications being administered, whether treatment is diagnostic, prognostic, prophylactic or therapeutic, and so on. Dosage may be determined using routine methods known to those of skill in the art in order to optimize safety and efficacy.
Clearly, an amount of a fusion peptide to be administered will also depend on the subject to which it is to be administered. In the case where the subject is a human, amount of a peptide to be administered will depend on a number of factors including the age of the patient, the severity of the condition and the past medical history of the patient and always lies within the sound discretion of the administering physician. Generally, a total daily dose of peptides of the invention administered to a human or other mammal in single or in divided doses can be in amounts, for example, of from 0.1 mg/Kg/day to 30 mg/Kg/day of the peptide, from 0.1 mg/Kg/day to 20 mg/Kg/day of the peptide, or from 2 mg/Kg/day to 10 mg/Kg/day of the peptide, in single or multiple doses. Single dose compositions may contain such amounts or submultiples thereof to make up a daily dose. In an embodiment, 5 mg/kg is given daily, intraperitoneally (IP).
Dosing regimens and formulations of INGAP peptide have been described (see, e.g., US application publication no. 2004/0132644).
In an embodiment, peptides of the invention are formulated or used in a pharmaceutically acceptable salt form. In a particular embodiment, the pharmaceutically acceptable salt is an acetate salt.
In an embodiment, peptides of the invention are substantially pure.
Stability may be determined using methods known in the art. For example, stability of peptides is determined by comparing various parameters including, but not limited to, degree of purity, total percentage of impurities, percentage of individual impurities (as determined by HPLC or other suitable quantitative method), appearance, and water content of a sample. An HPLC method can be used to determine any increase in levels of degradation products relative to levels of the therapeutic peptide.
Peptide samples, whether in solution or a lyophilized powder, may be stored at various temperatures, in the presence or absence of humidity, and in light or dark vials. Degradation during different storage conditions can lead to an increase in impurities and a decrease in therapeutic peptide content. In some embodiments, it is desirable that a sample preparation is more than 80% pure, more than 90% pure, more than 95% pure, or more than 97% pure.
Peptides of the present invention may also be administered as a component of a pharmaceutically administrable composition. In other words, a peptide may be present in a formulation for administration to a subject in need thereof. An inventive peptide may be the sole active ingredient for, e.g., treatment of diabetes. Alternatively, a composition may also contain one or more additional compounds, e.g., a second agent that may be used to treat the same or related conditions.
It should be understood that peptides of the invention can optionally be administered in combination with other agents that are effective in treating the disorder or condition in need of treatment. In keeping with the scope of the present disclosure, peptides and compositions of the invention may be used with other therapeutic or prophylactic agents. Peptides of the invention may be administered concomitantly or sequentially with a second agent. It should be understood that any therapeutic agent for Type 1 or Type 2 diabetes or related disorders is contemplated for use in combination with peptides of the invention. Examples of such therapeutic or prophylactic agents include, without limitation, antidiabetic agents such as metformin, sulphonylureas (e.g. glibenclamide, tolbutamide, glimepiride), nateglinide, repaglinide, thiazolidinediones (e.g. rosiglitazone, pioglitazone), PPAR-gamma-agonists (e.g. GI 262570) and antagonists, PPAR-gamma/alpha modulators (e.g. KRP 297), alpha-glucosidase inhibitors (e.g. acarbose, voglibose), DPPIV inhibitors (e.g. LAF237, MK-431), alpha2-antagonists, agents for lowering blood sugar, cholesterol-absorption inhibitors, HMGCoA reductase inhibitors (such as a statin), insulin and insulin analogues, GLP-1 and GLP-1 analogues (e.g. exendin-4) and/or amylin. In an embodiment, peptides and compositions of the invention are used in combination with the immune modulator anakinra, an IL-1 inhibitor approved for treatment of rheumatoid arthritis, but with evidence of efficacy in diabetes.
In one embodiment, a second therapeutic agent is an agent which preserves β-cell mass, for example by blocking cell death or apoptosis of β-cells, protecting islets against detrimental effects of IL-1, e.g., IL-1β, protecting against diabetogenic agents, and/or otherwise protecting or improving islet viability and/or function. A second therapeutic agent may also reverse insulin resistance, control intestinal glucose absorption, normalise hepatic glucose production, and/or improve beta-cell glucose sensing and insulin secretion. In one embodiment, a second therapeutic agent may be an inhibitor of the transcription factor NF-κB, or an inhibitor of the cytokine-induced activation of the transcription factor NF-κB. In an embodiment, a second therapeutic agent is anakinra In other embodiments, a second therapeutic agent is insulin, an insulin analogue, an SGLT 2 inhibitor, a new islet formation induces, a stem cell therapy, a T-lymphocyte inhibitor, an IL 12 activator, a STAT 4 activator, an immune modulator, an islet implant, an anti-inflammatory agent, an anti-CD3 monoclonal antibody, and/or an interleukin-1 (IL-1) receptor antagonist.
The present invention will be more readily understood by referring to the following examples, which are provided to illustrate the invention and are not to be construed as limiting the scope thereof in any manner.
Although pancreatic ductal cells have been understood to be a particular target of INGAP (Rosenberg, L., et al., 1988, Diabetes, 37: 334-341; Pittenger, G. L., et al., 2007, Pancreas, 34: 103-111), a number of studies including results of clinical trials suggest that β-cells are also responsive to INGAP stimulation. To study effects of INGAP on β-cells we used RIN-m5 F, a rat insulinoma cell line, commonly used as a β-cell surrogate in vitro (Cozar-Castellano, I., et al., 2008, Diabetes, 57: 3056-3068). Although no significant effect on insulin expression was observed in our experiments, the data showed that both INGAP-P and r-INGAP dose dependently induced BrdU incorporation in RIN-m5 F cells after 24 h (
Increase in BrdU incorporation was consistent with a rapid temporal activation of Erk½, observed between 1 and 15 min after addition of either r-INGAP or INGAP-P (
INGAP-19 and INGAP-19C peptides were also shown to induce Erk½ activation in RINm5F cells, and both were more effective than INGAP-P or INGAP-PC (
To determine how INGAP binds and internalizes into RIN-m5 F cells, we used r-INGAP labeled with fluorescent reactive dyes DyLight −488 (green) and −594 (red) and 5-FAM-labeled INGAP-P. As shown in
Interestingly, in chase experiments, when cells were exposed to DyLight488 rINGAP only for 1 h, followed by washing and culture without rINGAP for 5 or 24 h, the amount of internalized rINGAP was not significantly lower than after continuous incubation (
The lack of co-migration between rINGAP and CTB or Transferrin suggests that rINGAP is not internalized via either a clathrin- or caveolin-mediated pathway. This is in line with the results of immunostaining for clathrin and caveolin, showing no co-localization with rINGAP (
In contrast to r-INGAP and INGAP102-120, no accumulation or clustering of FAM-labeled INGAP104-118 was observed on the cell surface (
Besides differences in the dynamics of cell binding and internalization, some other differences between protein and peptide have been observed. For example, internalized INGAP-P appears to degrade faster, as shown in 24 h experiments with continuous and “chase” incubations (
To investigate whether rINGAP, INGAP102-120 and INGAP104-118 act via the same receptor, DyLight488-rINGAP and FAM-INGAP102-120 or INGAP104-118 were used in competition experiments with 20× molar excess of unlabeled protein or peptide. The results showed that internalization of the protein was partially inhibited by unlabeled protein and internalization of peptides was partially inhibited by unlabeled peptides, but they didn't appear to inhibit each other at concentrations tested (
To compare the potency of 19-mer extended peptides (19-mer seq1, seq2 and seq3; see Table 1) and the 15-mer INGAP-P peptide (see Table 1), Erk½ activation was measured in RINm5 F cells. Results are shown in
Activation of Erk½ may be mediated by a number of signaling cascades initiated at the cell membrane level by receptor tyrosine kinases (RTK) or by different classes of G-protein coupled receptors (GPCRs). These signaling cascades include PKC, PKA, PI3 K or Ras/Raf-dependent pathways. Since the nature of the INGAP receptor is unknown, we screened for both RTK and GPCR- initiated signaling events using phospho-specific antibodies and pharmacological inhibitors of the above-mentioned pathways. For comparison we used EGF (10 ng/ml) and Ex- 4 (10 nM), found to be mitogenic for RIN-m5 F cells at the indicated concentrations (
Activation of low molecular weight Ras family GTPases is the first key event in signaling through RTKs, such as EGFR. It became apparent, however, that mechanisms of MAP kinase activation by GPCRs may also include Ras activation by cross-talk between GPCRs and RTKs, e.g., transactivation of EGFR shown for several GPCR ligands, including GLP-1. In keeping with this notion, our results show a rapid Ras activation by both INGAP-P and rINGAP (
In addition to Ras activation, we observed an increase in Akt phosphorylation after 30 min of treatment with INGAP-P that was delayed relative to activation of Erk½ (
To investigate signaling events implicated in INGAP induced proliferation, we employed specific pharmacological inhibitors of Raf (Raf inhibitor 1), PI3 K (wortmannin), PKC (Bis), PKA (H89, PKi), Adenylate cyclase (SQ22536), Src (PP2) and EGFR (AG1478). In addition, Pertussis toxin (Ptx) was used to examine whether INGAP actions were mediated by a GPCR. Effectiveness of these inhibitors was judged by Erk½ phosphorylation after 10 min of treatment with INGAP or EGF or Ex-4, and by BrdU incorporation after 24 h.
As shown in
Aside from expected inhibition of Erk½ and BrdU incorporation by PD98059, no other inhibitor tested (for PKC, PI3 K, or PKA) significantly reduced Erk½ phosphorylation. Except for H89 (PKA inhibitor) causing reduction in BrdU incorporation in rINGAP-treated cells after 24 h, which is discussed below, no inhibition of proliferation was observed in other groups (
In contrast to the Erk½ data, an inhibitor of PKA (H89) reduced BrdU incorporation in rINGAP treated cells (
Our results suggest that a cAMP-PKA pathway is not involved in INGAP signaling. In this context, if INGAP indeed signals through a GPCR, the receptor is likely coupled to a G;-protein, which has an ability to inhibit adenylate cyclase (Luttrell, L. M., 2002,Can J Physiol Pharmacol, 80, 375-382).
Taken together, results presented herein show that both INGAP-P and rINGAP stimulate proliferation in RIN-m5 F cells by activating a Ras-Raf-Erk pathway. Both INGAP-P and rINGAP likely act via a G;-protein coupled receptor(s) that does not induce activation of cAMP.
Degradation profiles of INGAP-P and INGAP-19 peptides in presence of serum were determined (
Time-course studies of in vitro incubation of INGAP-PC and INGAP-19C peptides in FBS were also performed (
A 15-amino acid fragment of INGAP protein (amino acids 104-118) and a 19-amino acid fragment of INGAP protein (amino acids 102-120) were synthesized and HPLC-purified at the Sheldon Biotechnology Centre (McGill University, Montreal). A full-length recombinant INGAP (r-INGAP) containing C-terminal 6-His tag (MW 17.6 kDa) was cloned from hamster pancreatic tissue by directional cloning of a PCR product generated with Superscript III RT and Platinum™ Pfx DNA Polymerase (Invitrogen) into the pcDNA3.1D/V5-His-TOPO™ expression vector (Invitrogen). This construct was used for re-cloning into a lentiviral vector and expressed in H293 cells (as described in Assouline-Thomas, B., et al., 2010, Protein Expr Purif, 69: 1-8). Purification of r-INGAP was carried out using Cobalt resin (BD TALON™, BD Biosciences, or Fractogel EMD Chelate(M), Merck) as described (Assouline-Thomas, B., et al., 2010, Protein Expr Purif, 69: 1-8).
Cell culture
RIN-m5 F cells (passage 18) were purchased from ATCC and maintained at 37° C./5% CO2 in RPMI-1640 medium (Invitrogen) containing 25 mM glucose, 10% FBS (Montreal Biotech), and antibiotics/antimycotics (Invitrogen). Experiments were carried out on cells from passages 25-31.Cells were plated in 60 mm tissue culture dishes (1×106 cells per dish) and allowed to grow for 24-48 h, followed by serum withdrawal for 24 h prior to treatment with INGAP proteins or peptides. INGAP-P (15-mer peptide), INGAP-P2 (19-mer peptide), rINGAP, and EGF (10 ng/ml, Sigma) were administered in serum-free medium for the times indicated.
Cells plated in 8-well or 4-well chamber slides (5×104 or 1×105 cells per well) were treated for 24 h with INGAP, EGF or Ex 4, as described above, and 50 μM BrdU was added during the last 3 hours of treatment. Cells were washed with PBS and fixed in Methanol for 10 min at −20° C. Immunostaining for BrdU was carried out using mouse anti- BrdU antibody (Roche) following the manufacturer's protocol. This was followed by detection with secondary, HRP-conjugated antibody (broad spectrum, Histostain™-Plus) and AEC chromogen (both from Zymed Laboratories). Slides were counterstained with hematoxylin. BrdU-positive and negative nuclei were counted (total 200 per well) and the percentage of BrdU-positive nuclei was calculated (
Following treatments, cells were placed on ice, washed with PBS and solubilized in lysis buffer (Cell Signaling, Inc., Beverly, Mass.), containing 2.5 mM Na4 P2 O7 , 1 mM Na3VO4 and Complete protease inhibitor cocktail tablet (Roche). Equal amounts of protein (20-50 m, measured with DC Protein assay (Bio-Rad)) were resolved by 10% SDS-PAGE, followed by transfer onto Nitrocellulose membrane (Bio-Rad) at 250 mA for 90 min and analyzed with different antibodies. Anti-Erk½ (MAPK 44/42) and anti-phospho Erk½ (Thr202/ Tyr204) rabbit polyclonal antibodies were purchased from Cell Signaling. Following primary antibody incubation, blots were washed and then incubated in a secondary, anti-mouse or anti-rabbit HRP-conjugated antibody (Cell Signaling), and washed and developed using the ECL system (GE Healthcare). To analyze expression of several proteins on the same blot, membranes were first incubated with phospho-antibodies followed by stripping (0.2 M Glycine, 0.1% SDS, 0.05% Tween20, pH2.2) prior to probing with corresponding non-phospho primary antibodies.
Visualization of fluorescent rINGAP, INGAP102-120 and INGAP104-118
100 μg of rINGAP were labeled with DyLight-488 or DyLight-594 (ThermoScientific) as specified in the instructions. INGAP102-120 and INGAP104-118 were labeled with either 5-FAM or FITC during synthesis at the Sheldon Biotechnology Centre (McGill University, Montreal) or Canpeptide (Pointe Claire, Quebec). Fluorescent rINGAP(50 nM) or INGAP102-120 and INGAP104-118 (8.35-16.7 μM were added to RIN-m5F cells grown in glass chamber slides (Beckton-Dickinson or Lab-Tek), for various intervals followed by washing with PBS and fixation in 4% paraformaldehyde. Slides were mounted using VectaShield medium (Vector) or Prolong Gold (Invitrogen) with DAPI for counterstaining of nuclei and examined under confocal microscope Zeiss LSM 510 or Olympus FV10i. For live confocal imaging cells were grown in Nunc™ chambered coverglass slides (ThermoScientific). Nuclei were stained with 0.01% DAPI prior to incubation with INGAP followed by washing. Live imaging was carried out at 37° C. and 5% CO2.
Experiments were repeated at least three times. Results are expressed as means±SEM. Statistical analysis was performed with unpaired Student's t-test. A p-value of <0.05 was considered significant.
Procedure: Cell plating and treating:
Aspirate all FBS-containing medium from a plate of RINm5 F cells and pipette 10 mL of PBS into the plate in order to wash off the medium. Aspirate the PBS and pipette 600 μL of trypsin into the plate. Tilt the plate to ensure that the trypsin covers everything. Add 8 mL of FBS-containing medium to the plate and then collect the mixture of medium and cells into a 15 mL tube. Count the cells using a 1:1 dilution of cells and trypan blue using a hemocytometer under a microscope in order to determine the cell density. Calculate the amount of cells needed in each plate in order to get the wanted cell density of 5×105 cells/plate and plate the cells into 16-35 mm plates. Incubate cells for 3 days at 37°, 5% CO2. Switch the medium from serum-containing medium to FBS-free medium in order to serum starve the cells for 24 hours before treatment. Treat the 16 plates:
Incubate the plates for 48 hours and collect the cells from each plate through trypsinization and place each sample in its own Eppendorf tube.
Cell Viability Assays were conducted by mixing 5 μL of cell from 1 sample with 10 mL of the cell counting machine's salt solution in a vial Place the vial inside the probe. The machine will count the number of live cells. Repeat the cell count with all of the other cell samples, doing two separate counts per sample. Conduct a Bradford Assay as shown below in order to normalize the cell counts to total protein. The results are shown in Tables 1A-C below.
A Bradford assay was conducted to normalize the cell counts to total protein. The samples were centrifuged and the medium aspirated and replaced with 1 ml of PBS per tube and centrifuged again. The PBS was aspirated and replaced with 200 μL of RIPA lysis buffer. The centrifugation was repeated in a 4° C. room. 5 μL of 8 different “standard” concentrations of BSA dissolved in RIPA lysis buffer was pipetted, into the first three columns of a 96 well plate (triplicates of each concentration), the final concentration being a blank, only containing lysis buffer. These will be used later for calculation purposes. A duplicate of each protein sample was centriguged. About 2 mL of Bradford reagent was prepared by mixing together 2 mL of solution A from a Bio-Rad protein assay kit and 40 μL of solution S, also from the kit. 254, of the Bradford reagent was placed via pipette into each well 200 μL of solution B from the kit was placed into each well. The plates were shaken for 10 minutes in order to mix the solutions together (make sure there are no bubbles) and placed in a reader to calculate the absorbance of the each sample. The resulting values were entered into a spreadsheet. A standard curve was created using the already known concentration of the standards (x-values) and their absorbance values (y-values). The formula of the line of best fit was used to algebraically calculate the concentration of the samples by plugging in their absorbance values
Cells were plated in three 8-well chamber slides (1×105 cells per well) were treated with 15C INGAP 15 L INGAP, water or FBS and incubated overnight, and 50 82 M BrdU was added during the last 3 hours of treatment. Cells were washed with PBS and fixed in Methanol for 10 min at −20° C. Immunostaining for BrdU was carried out using mouse anti-BrdU antibody (Roche) following the manufacturer's protocol. This was followed by detection with secondary, HRP-conjugated antibody (broad spectrum, Histostain™-Plus) and AEC chromogen (both from Zymed Laboratories). Slides were counterstained with hematoxylin. BrdU-positive and negative nuclei were counted (total 200 per well) and the percentage of BrdU-positive nuclei was calculated. The results are shown in Tables 2A-C below.
Following the cell plating and treating procedure 16 plates were treated with different treatments and for different amounts of time:
Following incubation, the plates were washed 2 times with cold PBS to be sure that all of the INGAP treatment is removed from the plates. The cells were lysed by adding 200 μL of RIPA lysis buffer to each plate and placed on a shaker for approximately 20 minutes to ensure complete lysis. Protein samples were collected into Eppendorf tubes using a pipette and centrifuged at 16.1×1000 rpm for 20 minutes in a 4° C. room. The resulting supernatant was transferred into fresh tubes and a Bradford Assay conducted to determine the concentration of protein in each sample. Solve for the amount of protein needed when loading 15 μg total into each well of the gel. The samples were combined with loading buffer, heated at 100° C. for 5 minutes and placed into 2-10% acrylamide gels with 10 wells along with a ladder and run at 200 V for 50 minutes or until the blue protein front runs out the bottom. A double transfer sandwich was used to transfer the proteins from the gel onto a positively charged nitrocellulose membrane by running the transfer at 0.3A for 1 hour. This transfers the already-run proteins from the gel substance onto the membranes. The membrane was placed a clear container and the non-specific proteins blocked by soaking in 5% BSA TBST buffer for 1 hour, letting it sit on a shaker during this time. T
The blocking solution was removed and the membrane allowed to remain in a primary antibody solution (10 μL of rabbit anti-phospho-ERK antibody, which binds to phosphorylated ERK in 10 mL of 5% BSA TBST) and left it to shake overnight in a room at a temperature of 4° C. The primary antibody was removed and the membrane washed with ˜10 mL of 1 ×TBST buffer, letting it sit on the shaker for 10 minutes. The wash was repeated 3 times. The membrane was then placed in a secondary antibody solution (10 μL of goat anti-rabbit antibody, which binds to the primary antibody, in 10 mL of 5% BSA TBST, giving it a dilution factor of 1:1000) for 1 hour on the shaker at room temperature. This causes the protein to give off chemiluminescence, therefore it can be visualized using a machine. The membrane was treated with the secondary antibody twice. The membranes was covered with 1 mL of ECL solution for 5 minutes and placed into the chemi-doc machine which can visualize the phosphorylated ERK. The computer program Image Lab was used to quantify the bands of phospho-ERK on the gel.
Following quantification of phosphor-ERK, the membrane was washed with TBST to remove the ECL solution and the antibody process repeated with rabbit anti-ERK as the primary antibody instead of rabbit anti-phospho-ERK with the goal of quantifying total ERK instead of phospho-ERK. a total of 3 Western Blot trials. The results are shown in Tables 3A-C.
The objective of this study is to expedite development of more potent and stable analogs of INGAP-peptide, as a next generation of islet regenerating agents. INGAP-peptide contains 15 amino acids (aa), which appear to represent a bio-active segment of the full-length INGAP protein. In the preliminary phase of this research, we extended the 15-mer INGAP-peptide by adding two amino acids on each end, as per protein sequence, resulting in a 19-mer, which we also cyclisized by adding Cysteines on each terminus (total 21 aa). Similarly, we produced a cyclic version of 15-mer INGAP (total 17 aa).
The resulting four analogs were denoted as 15 L (original 15-mer peptide), 15C (cyclic version of 15 L); 19L (linear 19-mer) and 19C (cyclic 19-mer).
Although 15C was not included in the proposal of the awarded CIHR POP grant, which was focused on evaluation of the 19-mer analogs, we used the 15C peptide along in all experiments to obtain as much information as possible on the effect of cyclization and extension on INGAP's biological functions
According to the research design, the experiments with the INGAP analogs were carried out both in vitro (Aim1) and in vivo (Aim2).
Aim 1: Biological Effects of INGAP Analogs In Vitro
In this part of the study we used two cell lines previously shown to be responsive to INGAP-peptide and INGAP-protein:
HPDE Cells—Differentiation Assay
Pdx-1 (Pancreatic and duodenal homeobox 1) is expressed in the pancreatic duct epithelium cells during development, and seems to be a prerequisite for their differentiation into acini, ducts, and endocrine cells in the mature pancreas We investigated Pdx-1 gene expression in INGAP-treated HPDE cells.
There is a basal low level of Pdx-1 in adult pancreatic ductal cells. We have previously shown that the level of Pdx-1 mRNA increases after 15 minutes of treatment with 167 nM INGAP-P, this effect is rapidly followed by the induction of a cascade of transcription factors that lead to insulin expression, and therefore reflect a transdifferentiation of adult ductal cells towards a beta-like phenotype (effect described for INGAP-P in “Islet Neogenesis Associated Protein (INGAP) Induces the Differentiation of an Adult Human Pancreatic Ductal Cell line into Insulin-expressing Cells through Stepwise Activation of Key Transcription Factors for Embryonic Beta Cell Development.” Assouline et al, manuscript submitted to Differentiation).
Here we have compared the effect of the 4 different analogues on the expression of Pdx-1 by qPCR.
Referring to
Our data show that all 4 peptides do induce an increase of Pdx-1 expression after 15 minutes. The two more potent molecules at the concentration of 167 nM tested in this experiment are INGAP-P (15 L) and INGAP-19C which induce an increase of 3.49±0.70 fold and 3.10±0.48 fold respectively. INGAP-15C also induces a smaller increase of the level of Pdx-1 mRNA: 1.89±0.33 fold. INGAP-19 L induces an increase as well, but not significant at this time point.
In conclusion, all four peptides do increase Pdx-1 mRNA levels, what suggest at the light of our previous data with INGAP-P, that they all can instruct the cells to undergo the first steps of endocrine differentiation.
Proliferation Assay (RINm5F Cells
In the previous study, we showed that INGAP-peptide (15 L) dose-dependently increased proliferation of RIN-m5 F (by 60% after 24 h, BrdU assay) and activated Erk½ by phosphorylation on Thr202/ Tyr204that peaked at 10 min of treatment (Petropavlovskaia M et al., 2012, Am J Physiol Endocrinol Metab). The effect was observed at concentration of 167 nM and higher, whereas lower concentrations, e.g 16.7 nM, had no effect.
In the current study we assessed the proliferative effects of all four analogs on RIN cells by cell counting after 48 h and by measuring Erk phosphorylation in a time-course experiments. The analogs were used at 167 nM (1×) and 1.67 mM (10 ×) concentrations.
The results of the 48 h treatment by cell counting (
Referring to
Signaling events leading to the increase in proliferation, i.e., Erk phosphorylation, occur early after addition of INGAP. We compared the dynamics of Erk½ activation by the analogs in a time course experiments lasting up to 3 h (
As seen in
Analysis of the same samples for phosphorylation of another important signaling molecule implicated in cell proliferation and survival, Akt (PI3 kinase-Akt pathway), demonstrated an increase in Akt activation by all the analogs after 20 min of treatment which is sustained up to 3 h tested (
In conclusion, all INGAP analogs demonstrate the ability to stimulate cell proliferation in RINm5 F cells, consistent with activation of Erk½ and Akt. 19C appears to be slightly more effective, as compared with the other analogs (both cell numbers and Erk½ data). One of the possible explanations is that 19C is more stable (up to 48 h in culture medium, vs 4-6 h half-life for 15 L. 15C and 19 L, based on the preliminary HPLC data). If this is the case, lowering of the 19C concentration would be an interesting extension of these experiments, especially in view of potential clinical applications.
Effect of INGAP analogs on cytokine-induced apoptosis in RIN-m5 F
Since Akt activation has been implicated in cell survival, we tested whether all INGAP analogs assert an anti-apoptotic effect, previously shown for the INGAP protein by a PhD student in our lab. Using the model of cytokine-induced apoptosis (IL1+INFg, both 10 nM), which is mediated by activation of NfkB pathway followed by an increase in iNOS production, we have tested the analogs in 5 independent experiments, at 167 nM concentration. As shown in
Overall, the results of in vitro experiments show that each all INGAP analogs display a similar mode of action on HPDE and RINm5 F cells, with 19 being the most stable and potentially more effective analog than currently used 15 L. The data presented suggest that more studies are needed to investigate whether lower doses (and/or less frequent administration) of 19C makes it a more attractive islet regenerating drug.
Aim2:Biological Effects of INGAP Analog In Vivo, on the STZ-Induced Model of Diabetes in Mice.
In this part of the study, we used a well established model of STZ (streptozotocin)-induced diabetes, resulting in a substantial destruction of beta cell mass. Previous studies conducted in our lab have shown islet neogenic effects of INGAP-peptide (15 L) and INGAP protein after the 8-week administration daily.
Prior to the start of the STZ experiments, we tested the stability of INGAP analogs in the serum of non-diabetic mice by injecting 5-FAM labeled INGAP analogs (custom made at Canpeptide, Pointe Claire) at 500 mg/mouse IP . The analogs were FAM labeled to determine the post-injection time needed for the peptides to reach the pancreas and to potentially identify the target cells. Mice were sacrificed after 10 min, 30 min, 1 h and 2 h (three mice per group) and blood and tissue samples were collected for processing. Blood serum was precipitated with methanol (1:3) to remove serum proteins and the resulting supernatant was analyzed by HPLC to detect presence of INGAP peptides.
Examination of formalin-fixed, paraffin-embedded tissue at 1 h, indicated that only FAM-19C was clearly detectable in the pancreas, whereas presence of other analogs was not certain due to a relatively high level of autofluorescence. These experiments need to be repeated by using cryosections vs paraffin section to minimize a potential loss of the fluorescence.
Referring to
Of note, mice in all groups showed a high viability for 7 weeks, afterwards some losses of animals (13 mice) occurred but it was not always associated with hyperglycemia. The most likely other cause was inflammation associated with daily injections. This fact may have affected the average values of glycemia in most groups, except for 15C (no losses) and 19C (1 mouse lost). Decreasing frequency of injections would be therefore an important objective in the future experiments.
The weight of all diabetic mice proved to stay stable throughout, whereas Control Nondiabetic mice increased their weight by approximately 6 grams (data not shown).
As shown in
It should be noted that in the 19C group, the decline in fasting glycemia appeared to occur earlier than in other groups, at 3 weeks of treatment.
After 10 weeks of treatment, the animals were sacrificed and the pancreata were weighed and processed for RNA extraction (still ongoing) and Immunocytochemistry.
As shown in
Pancreata harvested at the end of the treatments were fixed in formalin and paraffin sections were stained for hematoxylin and eosin (H&E) to evaluate the morphologic changes that would suggest islet neogenesis.
The analysis of the H&E stained sections showed that for all 4 analogues, and as previously described for INGAP-P (15 L), the pancreases show neogenesis features, i.e. the presence of islets bulging from or attached to ducts (
Referring to
While the disclosure has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications and this application is intended to cover any variations, uses, or adaptations of the disclosure following, in general, the principles of the disclosure and including such departures from the present disclosures as come within known or customary practice within the art to which the disclosure pertains and as may be applied to the essential features herein before set forth, and as follows in the scope of the appended claims.
Unless defined otherwise or the context clearly dictates otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It should be understood that any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the invention.
The contents of all documents and references cited herein are hereby incorporated by reference in their entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CA2014/050104 | 2/14/2014 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 61765203 | Feb 2013 | US |
