|Publication number||USRE39299 E1|
|Application number||US 09/709,585|
|Publication date||Sep 19, 2006|
|Filing date||Nov 13, 2000|
|Priority date||Feb 22, 1995|
|Also published as||US5834590, WO1996026215A1|
|Publication number||09709585, 709585, US RE39299 E1, US RE39299E1, US-E1-RE39299, USRE39299 E1, USRE39299E1|
|Inventors||Aaron I. Vinik, Gary L. Pittenger, Ronit Rafaeloff-Phail, Lawrence Rosenberg, William P. Duguid|
|Original Assignee||Eastern Virginia Medical School Of The Medical College Of Hampton Roads, Mcgill University|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (3), Non-Patent Citations (17), Referenced by (18), Classifications (18), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a reissue application of U.S. Pat. No. 5,834,590, filed as application Ser. No. 08/401,530 on Feb. 22, 1995.
Pancreatic islets of Langerhans are the only organ of insulin production in the body. However, they have a limited capacity for regeneration. This limited regeneration capacity predisposes mammals to develop diabetes mellitus. Thus there is a need in the art of endocrinology for products which can stimulate the regeneration of islets of Langerhans to prevent or ameliorate the symptoms of diabetes mellitus.
One model of pancreatic islet cell regeneration involves cellophane-wrapping of the pancreas in the Syrian golden hamster (1). Wrapping of the pancreas induces the formation of new endocrine cells which appear to arise from duct epithelium (2-4). There is a need in the art to identify and isolate the factor(s) which is responsible for islet cell regeneration.
It is an object of the invention to provide a preparation of a mammalian protein or polypeptide portions thereof involved in islet cell neogenesis.
It is another object of the invention to provide a DNA molecule encoding a mammalian protein involved in islet cell neogenesis.
It is yet another object of the invention to provide a preparation of a mammalian INGAP (islet neogenesis associated protein) protein.
It is still another object of the invention to provide nucleotide probes for detecting mammalian genes involved in islet cell neogenesis,
It is an object of the invention to provide a method for isolation of INGAP genes from a mammal.
It is another object of the invention to provide an antibody preparation which is specifically immunoreactive with an INGAP protein.
It is yet another object of the invention to provide methods of producing INGAP proteins.
It is an object of the invention to provide methods for treating diabetic mammals.
It is another object of the invention to provide methods for growing pancreatic islet cells in culture.
It is still another object of the invention to provide methods of enhancing the life span of pancreatic islet cells encapsulated in polycarbon shells.
It is an object of the invention to provide methods of enhancing the number of pancreatic islet cells in a mammal.
It is an object of the invention to provide transgenic mammals.
It is another object of the invention to provide genetically engineered mammals.
It is yet another object of the invention to provide methods of identifying individual mammals at risk for diabetes.
It is an object of the invention to provide methods of detecting INGAP protein in a sample from a mammal.
It is still another object of the invention to provide a method of treating isolated islet cells to avoid apoptosis.
It is another object of the invention to provide methods of treating mammals receiving islet cell transplants.
It is an object of the invention to provide a method of inducing differentiation of β cell progenitors.
It is an object of the invention to provide a method of identifying β cell progenitors.
It is another object of the invention to provide a method of treating a mammal with pancreatic endocrine failure.
It is an object of the invention to provide antisense constructs for regulating the expression of INGAP.
It is yet another object of the invention to provide a method for treating nesidioblastosis.
It is still another object of the invention to provide kits for detecting mammalian INGAP proteins.
It is an object of the invention to provide pharmaceutical compositions for treatment of pancreatic insufficiency.
These and other objects of the invention are provided by one or more of the embodiments described below.
In one embodiment a preparation of a mammalian INGAP protein is provided. The preparation is substantially free of other mammalian proteins.
In another embodiment an isolated cDNA molecule is provided. The cDNA molecule encodes a mammalian INGAP protein.
In still another embodiment of the invention a preparation of a mammalian INGAP protein is provided. The preparation is made by the process of:
In yet another embodiment of the invention a nucleotide probe is provided. The probe comprises at least 20 contiguous nucleotides of the sequence shown in SEQ ID NO: 1.
In another embodiment of the invention a preparation of INGAP protein of a mammal is provided. The preparation is substantially purified from other proteins of the mammal. The INGAP protein is inducible upon cellophane-wrapping of pancreas of the mammal.
In yet another embodiment of the invention a method of isolating an INGAP gene from a mammal is provided. The method comprises:
hybridizing one or more oligonucleotides comprising at least 10 contiguous nucleotides of the sequence shown in SEQ ID NO: 1 to genomic DNA or cDNA of said mammal;
identifying DNA molecules from said genomic DNA or cDNA which hybridize to said one or more oligonucleotides.
In still another embodiment of the invention an isolated cDNA molecule is provided. The cDNA molecule is obtained by the process of:
In another embodiment of the invention an antibody is provided. The antibody is specifically immunoreactive with a mammalian INGAP protein.
According to still another embodiment of the invention a method of producing a mammalian INGAP protein is provided. The method comprises the steps of:
providing a host cell transformed with a cDNA encoding a mammalian INGAP protein;
culturing the host cell in a nutrient medium so that the INGAP protein is expressed; and
harvesting the INGAP protein from the host cell or the nutrient medium.
According to yet another embodiment of the invention a method of producing a mammalian INGAP protein is provided. The method comprises the steps of: providing a host cell comprising a DNA molecule obtained by the process of:
culturing the host cell in a nutrient medium so that the mammalian INGAP protein is expressed; and
harvesting the mammalian INGAP protein from the host cells or the nutrient medium.
According to another embodiment of the invention a method of treating diabetic mammals is provided. The method comprises:
administering to a diabetic mammal a therapeutically effective amount of an INGAP protein to stimulate growth of islet cells.
According to another embodiment of the invention a method of growing pancreatic islet cells in culture is provided. The method comprises:
supplying an INGAP protein to a culture medium for growing pancreatic islet cells; and
growing islet cells in said culture medium comprising INGAP protein.
According to another embodiment of the invention a method of enhancing the life span of pancreatic islet cells encapsulated in a polycarbon shell is provided. The method comprises:
adding to encapsulated pancreatic islet cells an INGAP protein in an amount sufficient to enhance the survival rate or survival time of said pancreatic islet cells.
According to another embodiment of the invention a method of enhancing the number of pancreatic islet cells in a mammal is provided. The method comprises:
administering a DNA molecule which encodes an INGAP protein to a pancreas in a mammal.
According to another embodiment of the invention a method of enhancing the number of pancreatic islet cells in a mammal is provided. The method comprises:
administering an INGAP protein to a pancreas in a mammal.
According to another embodiment of the invention a transgenic mammal is provided. The mammal comprises an INGAP gene of a second mammal.
According to another embodiment of the invention a non-human mammal is provided. The mammal has been genetically engineered to contain an insertion or deletion mutation of an INGAP gene of said mammal.
According to another embodiment of the invention a method of identifying individual mammals at risk for diabetes is provided. The method comprises:
identifying a mutation in an INGAP gone of a sample of an individual mammal, said mutation causing a structural abnormality in an INGAP protein encoded by said gene or causing a regulatory defect leading to diminished or obliterated expression of said INGAP gene.
According to another embodiment of the invention a method of detecting INGAP protein in a sample from a mammal is provided. The method comprises:
According to another embodiment of the invention a method of treating isolated islet cells of a mammal to avoid apoptosis of said cells is provided. The method comprises:
According to another embodiment of the invention a method of treating a mammal receiving a transplant of islet cells is provided. The method comprises:
According to another embodiment of the invention a method of inducing differentiation of β cell progenitors is provided. The method comprises:
In yet another embodiment of the invention a method is provided for identification of β cell progenitors. The method comprises:
According to another embodiment of the invention a method of treating a mammal with pancreatic endocrine failure is provided. The method comprises:
According to another embodiment of the invention an antisense construct of a mammalian INGAP gene is provided. The construct comprises:
According to another embodiment of the invention a method of treating nesidioblastosis is provided. The method comprises:
According to another embodiment of the invention a kit for detecting a mammalian INGAP protein in a sample from a mammal is provided. The kit comprises:
According to another embodiment of the invention a pharmaceutical composition for treatment of pancreatic insufficiency is provided. The composition comprises:
According to another embodiment of the invention a pharmaceutical composition is provided. The composition comprises:
These and other embodiments of the invention provide the art with means of stimulating and inhibiting islet cell neogenesis Means of diagnosis of subsets of diabetes mellitus are also provided by this invention.
FIG. 2. Comparison of amino acid sequences of INGAP SEQ ID NO:2, rat PAP-I (PAP-I) (18) SEQ ID NO: 3, Human PAP/HIP (PAP-H/HIP)(10, 11) SEQ ID NO:4, rat PAP-Ill (PAP III)(9) SEQ ID NO: 5, rat PAP-II (PAP-R)(8) SEQ ID NO:6, Rat Reg/PSP/Lithostatine (REG/LITH)(13, 15) SEQ ID NO: 7 and the invariable motif found by Drickamer in cell members of C-type lectins (Drickamer) (12). Six conserved cysteines are marked by asterisks and the 2 putative N-glycosylation sites of INGAP are underlined and in bold letters.
PREFERRED EMBODIMENTS We now report the identification of a gene, INGAP, that shows staining homology to the pancreatitis associated protein (PAP) family of genes (7-11). The predicted protein shares the carbohydrate recognition domain (CRD) of the calcium dependent C-type lectins as defined by Drickamer (12). INGAP protein plays a role in stimulation of islet neogenesis, in particular, in beta cell regeneration from ductal cells.
The cDNA sequence of a mammalian INGAP is provided in SEQ ID NO: 1. The predicted amino acid sequence is shown in SEQ ID NO:2. These sequences were determined from nucleic acids isolated from hamster, but it is believed that other mammalian species will contain INGAP genes which are quite similar. For example, one would expect homologous genes to contain at least about 70% identity. Closer species would be expected to have at least about 75%, 80%, or even 85% identity. In contrast, other family members of the calcium dependent C-type lectins contain at most 60% identity with INGAP.
The DNA sequence provided herein can be used to form vectors which will replicate the gene in a host cell, and may also express INGAP protein. DNA sequences which encode the same amino acid sequence as shown in SEQ ID NO:2 can also be used, without departing from the contemplation of the invention. DNA sequences coding for other mammalian INGAPs are also within the contemplation of the invention. Suitable vectors, for both prokaryotic and eukaryotic cells, are known in the art. Some vectors are specifically designed to effect expression of inserted DNA segments downstream from a transcriptional and translational control site. One such vector for expression in eukaryotic cells employs EBNA His, a plasmid which is available commercially from InVitrogen Corp. The loaded vector produces a fusion protein comprising a portion of a histidine biosynthetic enzyme and INGAP Mother vector, which is suitable for use in prokaryotic cells, is pCDNA3. Selection of a vector for a particular purpose may be made using knowledge of the properties and features of the vectors, such as useful expression control sequences. Vectors may be used to transform or transfect host cells, either stably or transiently. Methods of transformation and transfection are known in the art, and may be used according to suitability for a particular host cell. Host cells may be selected according to the purpose of the transfection. A suitable prokaryotic host is E. coli DH5a. A suitable eukaryotic host is cos7, an African Green Monkey kidney cell line. For some purposes, proper glycosylation of INGAP may be desired, in which case, a suitable host cell should be used which recognizes the glycosylation signal of INGAP
Probes comprising at least 10, 15, 20, or 30 nucleotides of contiguous sequence according to SEQ ID NO: 1 can be used for identifying INGAP genes in particular individuals or in members of other species. Appropriate conditions for hybridizations to same or different species' DNA an known in the art as high stringency and low stringency, respectively. These can be used in a variety of formats according to the desired use. For example, Southern blots, Northern blots, and in situ colony hybridization, can be used as these are known in the art. Probes typically an DNA or RNA oligomers of at least 10, 15, 20, or 30 nucleotides. The probe may be labeled with any detectable moiety known in the art, including radiolabels, fluorescent labels, enzymes, etc. Probes may also be derived from other mammalian INGAP gene sequences.
INGAP genes can be isolated from other mammals by utilizing the nucleotide sequence information provided herein. (More laboriously, they can be isolated using the same method described in detail below for isolation of the hamster INGAP gene.) Oligonucleotides comprising at least 10 contiguous nucleotides of the disclosed nucleotide sequence of INGAP are hybridized to genomic DNA or cDNA of the mammal. The DNA may conveniently be in the form of a library of clones. The oligonucleotides may be labelled with any convenient label, such as a radiolabel or an enzymatic or fluorescence label. DNA molecules which hybridize to the probe one isolated. Complete genes can be constructed by isolating overlapping DNA segments, for example using the first isolated DNA as a probe to contiguous DNA in the library or preparation of the mammal's DNA. Confirmation of the identity of the isolated DNA can be made by observation of the pattern of expression of the gene in the pancreas when subjected to cellophane wrapping, for example. Similarly, the biological effect of the encoded product upon pancreatic ductal cells will also serve to identify the gene as an INGAP gene.
If two oligonucleotides are hybridized to the genomic DNA or cDNA of the mammal then they can be used a primers for DNA synthesis, for example using the polymerase chain reaction or the ligase chain reaction. Construction of a full-length gene and confirmation of the identity of the isolated gene can be performed as described above.
INGAP protein may be isolated according to the invention by inducing mammalian pancreatic cells to express INGAP protein by means of cellophane-wrapping. This technique is described in detail in reference no. 1 which is expressly incorporated herein. Briefly, the pancreas is exposed and a strip of sterile cellophane tape is wrapped carefully around the head of the gland, so as not to crush the underlying tissue. Duct ligation is not involved. INGAP protein so produced may be purified from other mammalian proteins by means of immunoaffinity techniques, for example, or other techniques known in the art of protein purification. An antibody specific for a mammalian INGAP is produced using all, or fragments of, the amino acid sequence of an INGAP protein, such as shown in SEQ ID NO: 2, as immunogens. The immunogens can be used to identify and purify immunoreactive antibodies. Monoclonal or polyclonal antibodies can be made as is well known in the art. The antibodies can be conjugated to other moieties, such as detectable labels or solid support materials. Such antibodies can be used to purify proteins isolated from mammalian pancreatic cells or from recombinant cells. Hybridomas which secrete specific antibodies for an INGAP protein are also within the contemplation of the invention.
Host cells as described above can be used to produce a mammalian INGAP protein. The host cells comprise a DNA molecule encoding a mammalian INGAP protein. The DNA can be according to SEQ ID NO:1, or isolated from other mammals according to methods described above. Host cells can be cultured in a nutrient medium under conditions where INGAP protein is expressed. INGAP protein can be isolated from the host cells or the nutrient medium, if the INGAP protein is secreted from the host cells.
It has now been found that INGAP and fragments thereof are capable of inducing and stimulating islet cells to grow. Moreover, they are capable of inducing differentiation of pancreatic duct cells, and of allowing such cells to avoid the apoptotic pathway. Thus many therapeutic modalities are now possible using INGAP fragments thereof, and nucleotide sequences encoding INGAP Therapeutically effective amounts of INGAP are supplied to patient pancreata, to isolated islet cells, and to encapsulated pancreatic islet cells, such as in a polycarbon shell. Suitable amounts of INGAP for therapeutic purposes range from 1-150 μg/kg of body weight or in vitro from 1-10,000 μg/ml. Optimization of such dosages can be ascertained by routine testing. Methods of administering INGAP to mammals can be any that are known in the art, including subcutaneous, via the portal vein, by local perfusion, etc.
Conditions which can be treated according to the invention by supplying INGAP include diabetes mellitus, both insulin dependent and non-insulin dependent, pancreatic insufficiency, pancreatic failure, etc. Inhibition of INGAP expression can be used to treat nesidioblastosis.
According to the present invention, it has now been found that a small portion of INGAP is sufficient to confer biological activity. A fragment of 20 amino acids of the sequence of SEQ ID NO: 2, from amino acid #103-#122 is sufficient to stimulate pancreatic ductal cells to grow and proliferate. The effect has been seen on a rat tumor duct cell line, a hamster dad cell line, a hamster insulinoma cell line, and a rat insulinoma cell line. The analogous portions of other mammalian INGAP proteins are quite likely to have the same activity. This portion of the protein is not similar to other members of the pancreatitis associated protein (PAP) family of proteins. It contains a glycosylation site and it is likely to be a primary antigenic site of the protein as well. This fragment has been used to immunize mice to generate monoclonal antibodies.
The physiological site of expression of INGAP has been determined INGAP is expressed in acinar tissue, in the exocrine portion of the pancreas. It is not expressed in ductal or islet cells, i. e., the paracrine portion of the pancreas. Expression occurs within 24-48 hours of induction by means of cellophane wrapping.
Transgenic animals according to the present invention are mammals which carry an INGAP gene from a different mammal. The transgene can be expressed to a higher level than the endogenous INGAP genes by judicious choice of transcription regulatory regions. Methods for making transgenic animals are well-known in the art, and any such method can be used. Animals which have been genetically engineered to carry insertions, deletions, or other mutations which alter the structure of the INGAP protein or regulation of expression of INGAP are also contemplated by this invention. The techniques for effecting these mutations are known in the art.
Diagnostic assays are also contemplated within the scope of the present invention. Mutations in INGAP can be ascertained in samples such as blood, amniotic fluid, chorionic villus, blastocyst, and pancreatic cells. Such mutations identify individuals who are at risk for diabetes. Mutations can be identified by comparing the nucleotide sequence to a wild-type sequence of an INGAP gene. This can be accomplished by any technique known in the art, including comparing restriction fragment length polymorphisms, comparing polymerise chain reaction products, nuclease protection assays, etc. Alternatively, altered proteins can be identified, e.g., immunologically or biologically.
The present invention also contemplates the use of INGAP antisense constructs for treating nesidioblastosis, a condition characterized by overgrowth of β cells. The antisense construct is administered to a mammal having nesidioblastosis, thereby inhibiting the overgrowth of β cells. An antisense construct typically comprises a promoter, a terminator, and a nucleotide sequence consisting of a mammalian INGAP gene. The INGAP sequence is between the promoter and the terminator and is inverted with respect to the promoter as it is expressed naturally. Upon expression from the promoter, an mRNA complementary to native mammalian INGAP is produced.
Immunological methods for assaying INGAP in a sample from a mammal are useful, for example, to monitor the therapeutic administration of INGAP. Typically an antibody specific for INGAP will be contacted with the sample and the binding between the antibody and any INGAP in the sample will be detected This can be by means of a competitive binding assay, in which the incubation mixture is spiked with a known amount of a standard INGAP preparation, which may conveniently be detectably labeled. Alternatively, a polypeptide fragment of INGAP may be used as a competitor. In one particular assay format, the antibodies are bound to a solid phase or support, such as a bead, polymer matrix, or a microtiter plate.
According to the present invention, pancreatic duct cells of a mammal with pancreatic endocrine failure an be removed from the body and treated in vitro. The duct cells typically comprise β cell progenitors. Thus treatment with a preparation of a mammalian INGAP protein will induce differentiation of the β cell progenitors. The duct cells are contacted with a preparation of a mammalian INGAP protein substantially free of other mammalian proteins. The treated cells can then used as an autologous transplant into the mammal from whom they were derived. Such an autologous treatment minimizes adverse host versus graft reactions involved in transplants.
INGAP protein can also be used to identify those cells which bear receptors for INGAP. Such cells are likely to be the β cell progenitors, which are sensitive to the biological effects of INGAP. INGAP protein can be detestably labeled, such as with a radiolabel or a fluorescent label, and then contacted with a population of cells from the pancreatic duct. Cells which bind to the labeled protein will be identified as those which bear receptors for INGAP, and thus are β cell progenitors. Fragments of INGAP can also be used for this purpose, as can immobilized INGAP which can be used to separate cells from a mixed population of cells to a solid support. INGAP can be immobilized to solid phase or support by adsorption to a surface, by means of an antibody, or by conjugation. Any other means as is known in the art can also be used.
Kits are provided by the present invention for detecting a mammalian INGAP protein in a sample. This maybe useful, inter alia, for monitoring metabolism of INGAP during therapy which involves administration of INGAP to a mammal. The kit will typically contain an antibody preparation which is specifically immunoreactive with a mammalian INGAP protein. The antibodies may be polyclonal or mono-clonal. If polyclonal they may be affinity purified to tender them monospecific. The kit will also typically contain a polypeptide which has at least 15 consecutive amino acids of a mammalian INGAP protein The polypeptide is used to compete with the INGAP protein in a sample for binding to the antibody. Desirably the polypeptide will be detectably labeled. The polypeptide will contain the portion of INGAP to which the antibody binds. Thus if the antibody is monoclonal, the polypeptide will successfully compete with INGAP by virtue of it containing the epitope of the antibody. It may also be desirable that the antibodies be bound to a solid phase or support, such as polymeric beads, sticks, plates, etc.
Pharmaceutical compositions containing a mammalian INGAP protein may be used for treatment of pancreatic insufficiency. The composition may alternatively contain a polypeptide which contains a sequence of at least 15 consecutive amino acids of a mammalian INGAP protein. The polypeptide will contain a portion of INGAP which is biologically active in the absence of the other portions of the protein. The polypeptide may be part of a larger protein, such as a genetic fusion with a second protein or polypeptide. Alternatively, the polypeptide may be conjugated to a second protein, for example, by means of a cross-linking agent. Suitable portions of INGAP proteins may be determined by homology with amino acids #103 to #122 of SEQ ID NO:2, or by the ability of test polypeptides to stimulate pancreatic duct cells to grow and proliferate. As is known in the art, it is often the case that a relatively small number of amino acids can be removed from either end of a protein without destroying activity. Thus it is contemplated within the scope of the invention that up to about 10% of the protein can be deleted, and still provide essentially all functions of INGAP Such proteins have at least about 130 amino acids, in the case of hamster INGAP.
The pharmaceutical composition will contain a pharmaceutically acceptable diluent or carrier. A liquid formulation is generally preferred. INGAP may be formulated at different concentrations or using different formulants. For example, these formulants may include oils, polymer; vitamins, carbohydrates, amino acids, salts, buffers, albumin, surfactants, or bulking agents. Preferably carbohydrates include sugar or sugar alcohols such as mono-, di-, or polysaccharides, or water soluble glucans. The saccharides or glucans can include fructose, dextrose, lactose, glucose, mannose, sorbose, xylose, maltose, sucrose, dextran, pullulan, dextrin, alpha and beta cyclodextrin, soluble starch, hydroxethyl starch and carboxymethylcelloluose, or mixtures thereof. Sucrose is most preferred. Sugar alcohol is defined as a C4 to C8 hydrocarbon having an —OH group and includes galactitol, inositol, mannitol, xylitol, sorbitol, glycerol, and arabitol. Mannitol is most preferred. These sugars or sugar alcohols mentioned above may be used individually or in combination. There is no fixed limit to amount used as long as the sugar or sugar alcohol is soluble in the aqueous preparation. Preferably, the sugar or sugar alcohol concentration is between 1.0 w/v % and 7.0 w/v %, more preferable between 2.0 and 6.0 w/v %. Preferably amino acids include levorotary (L) forms of camitine, arginine, and betaine; however, other amino acids may be added. Preferred polymers include polyvinylpyrrolidone (PVP) with an average molecular weight between 2,000 and 3,000, or polyethylene glycol (PEG) with an average molecular weight between 3,000 and 5,000. It is also preferred to use a buffer in the composition to minimize pH changes in the solution before lyophilization or after reconstitution, if these are used. Most any physiological buffer may be used, but citrate, phosphate, succinate, and glutamate buffers or mixtures thereof are preferred. Preferably, the concentration is from 0.01 to 0.3 molar. Surfactants can also be added to the formulation.
Additionally, INGAP or polypeptide portions thereof can be chemically modified by covalent conjugation to a polymer to increase its circulating half-life, for example. Preferred 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. Preferred polymers an 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. Preferably, the protective group has between 1 and 8 carbons, more preferably it is methyl. The symbol n is a positive integer, preferably between 1 and 1,000, more preferably between 2 and 500. The PEG has a preferred average molecular weight between 1000 and 40,000, more preferably between 2000 and 20,000, most preferably between 3,000 and 12,000. Preferably, PEG has at least one hydroxy group, more preferably it is a terminal hydroxy group. It is this hydroxy group which is preferably activated to react with a free amino group on the inhibitor.
After the liquid pharmaceutical composition is prepared, it is preferably 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, the 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, the composition is preferably administered to subjects using those methods that are known to those skilled in the art.
The following examples are not intended to limit the scope of the invention, but merely to exemplify that which is taught above.
This example describes the cloning and isolation of a cDNA encoding a novel, developmentally regulated, pancreatic protein.
We hypothesized that a unique locally produced factor(s) is responsible for islet cell regeneration. Using the recently developed mRNA differential display technique (5,6) to compare genes differentially expressed in cellophane wrapped (CW) versus control pancreata (CP) allowed us to identify a cDNA clone (RD19-2) which was uniquely expressed in cellophane wrapped pancreas.
A cDNA library was constructed from mRNA isolated from cellophane wrapped hamster pancreas using oligo d(T) primed synthesis, and ligation into pcDNA3 vector (Invitrogen). The number of primary recombinants in the library was 1.2×104 with an average size of 1.1 kb. The cDNA library was screened for clones of interest using high density colony plating techniques. Colonies were lifted onto nylon membranes (Schleicher & Schnell) and further digested with proteinase K (50(g/ml). Treated membranes were baked at 80° C. for 1 hour and hybridized at 50° C. for 16-18 hours with 1−5×106 cpm/ml of [(32P]-dCTP(Dupont-NewEngland Nuclear) radiolabeled RD19-2 probe. Colonies with a positive hybridization signal were isolated, compared for size with Northern mRNA transcript, and sequenced to confirm identity with the RD19-2 sequence.
This example compares the sequence of INGAP to other proteins with which it shares homology.
The nucleotide sequence of the hamster INGAP clone with the longest cDNA insert was determined. As shown in
This example demonstrates the temporal expression pattern of INGAP upon cellophane-wrapping.
In order to determine the temporal expression of the INGAP gene, total RNA extracted from CP and CW pancreas was probed with the hamster INGAP cDNA clone in Northern blot analysis. A strong single transcript of 900 bp was detected (
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4965188 *||Jun 17, 1987||Oct 23, 1990||Cetus Corporation||Process for amplifying, detecting, and/or cloning nucleic acid sequences using a thermostable enzyme|
|US5834214||Dec 23, 1993||Nov 10, 1998||Institut National De La Sante Et De La Recherche Medicale||Detection of pancreatitis-associated protein for screening for cystic fibrosis|
|WO1994015218A1||Dec 23, 1993||Jul 7, 1994||Inst Nat Sante Rech Med||Detection of cystic fibrosis or a cftr gene mutation|
|1||*||Bradley et al., "BoiTechnology, Modifying the Mouse", Design and Desire 10:534-539 (1992).|
|2||Dusetti et al., Molecular Cloning, Genomic Organization, and Chromosomal Localization of the Human Pancreatitis-Associated Protein (PAP) Gene, Genomics, vol. 19, Jan. 1994, pp. 108-114.|
|3||International Search Report dated Jun. 23, 2000, Appl. No. EP 96905368, pp. 1-3.|
|4||*||Lasserre et al., "A Novel Gene (HIP) Activated in Human Primary Liver Cancer", Cancer Research 52:5089-5095 (1992).|
|5||*||Liang et al., "Distribution and Cloning of Eukaryotic mRNAs by Means of Differential Display: Refinements and Optimization", Nucleic Acids Research 21(14):3269-3275 (1993).|
|6||*||Miller et al., "Human Gene Therapy Comes of Age", Nature 357:455-460 (1992).|
|7||*||Orelle et al., "Human Pancreatitis-associated Protein" J. Clin. Invest. 90:2284-2291 (1992).|
|8||*||Pittenger GL. Et al. (1992) The Partial Isolation and Characterization of Ilotropin, a Novel Islet-Specific Growth Factor (abstract) Adv. Exp. Med. Biol. 321, pp. 123-132.|
|9||*||Rosenberg et al., "Reversal of Diabetes by the Induction of Islet Cell Neogenesis", Transplantation Proceedings 24(3):1027-1028 (1992).|
|10||*||Rosenberg et al., (1992) Pancreatic Islet Cell Regeneration and Growth. Ed. Al Vinik, Plenum Press, New York, pp. 95-104.|
|11||*||Rouquier et al., "Rat Pancreatic Stone Protein Messenger RNA", J. Biol. Chem., 266(2):786-791 (1991).|
|12||*||Stein et al., "Antisense Oligonucleotides as Therapeutic Agents-Is the Bullet Really Magical?", Science 261:1004-1012 (1993).|
|13||*||Terazono et al., "A Novel Gene Activated in Regenerating Islets", J. Biol. Chem., 263(5):211-2114 (1988).|
|14||*||Vinik et al., "Factors Controlling Pancreatic Islet Neogenesis", Yale Journal of Biology and Medicine 65:471-491 (1992).|
|15||Vinik, M.D. et al., "Factors Controlling Pancreatic Islet Neogenesis", The Yale Journal of Biology and Medicine, Inc., vol. 65, 1992, pp. 471-491.|
|16||Vinik, M.D. et al., "Factors Controlling Pancreatic Islet Neogenesis", Tumor Biology, vol. 14, 1993, pp. 184-200.|
|17||*||Watanabe et al., "Pancreatic Beta-Cell Replication and Amelioration of Surgical Diabetes by Reg Protein", Proc. Natl. Acad. Sci. USA 91:3589-3592 (1994).|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7393919||May 25, 2006||Jul 1, 2008||Cure Dm, Inc.||Peptides, derivatives and analogs thereof, and methods of using same|
|US7714103||May 15, 2008||May 11, 2010||Curedm, Inc.||Peptides, derivatives and analogs thereof, and methods of using same|
|US7989415||Dec 10, 2009||Aug 2, 2011||Curedm Group Holdings, Llc||Peptides, derivatives and analogs thereof, and methods of using same|
|US8012928||Dec 18, 2009||Sep 6, 2011||The Research Foundation Of State University Of New York||Truncated PAP2 and methods of making and using same|
|US8211430||Mar 3, 2006||Jul 3, 2012||Curedm Group Holdings, Llc||Methods and pharmaceutical compositions for treating type 1 diabetes mellitus and other conditions|
|US8361960||Sep 8, 2009||Jan 29, 2013||Ottawa Hospital Research Institute||Periostin-induced pancreatic regeneration|
|US8383578||Jun 24, 2011||Feb 26, 2013||Curedm Group Holdings, Llc||Peptides, derivatives and analogs thereof, and methods of using same|
|US8785400||Nov 21, 2007||Jul 22, 2014||Curedm Group Holdings, Llc||Methods and compositions relating to islet cell neogenesis|
|US8816047||Aug 29, 2008||Aug 26, 2014||Cure DM Group Holdings, LLC||Compositions and methods of using proislet peptides and analogs thereof|
|US8829158||Jan 18, 2013||Sep 9, 2014||Curedm Group Holdings, Llc||Peptides, derivatives and analogs thereof, and methods of using same|
|US20060198839 *||Mar 3, 2006||Sep 7, 2006||Levetan Claresa S||Methods and pharmaceutical compositions for treating type 1 diabetes mellitus and other conditions|
|US20070087971 *||May 25, 2006||Apr 19, 2007||Levetan Claresa S||Peptides, derivatives and analogs thereof, and methods of using same|
|US20080300190 *||May 15, 2008||Dec 4, 2008||Curedm, Inc.||Peptides, derivatives and analogs thereof, and methods of using same|
|US20090068145 *||Nov 21, 2007||Mar 12, 2009||Curedm, Inc.||Methods and Compositions Relating to Islet Cell Neogenesis|
|US20090142338 *||Sep 7, 2007||Jun 4, 2009||Curedm, Inc.||Methods and Compositions for Treating Type 1 and Type 2 Diabetes Mellitus and Related Conditions|
|US20100093605 *||Dec 10, 2009||Apr 15, 2010||Curedm, Inc.||Peptides, derivatives and analogs thereof, and methods of using same|
|US20100158809 *||Dec 18, 2009||Jun 24, 2010||The Research Foundation Of State University Of New York||Truncated pap2 and methods of making and using same|
|EP2407536A1||Dec 12, 2007||Jan 18, 2012||Bioaxone Therapeutique Inc.||ADP-ribosyl transferase fusion variant proteins|
|U.S. Classification||512/2, 435/69.7, 435/69.1, 424/198.1, 530/412, 530/350, 514/21.4, 514/21.2|
|International Classification||C07K14/00, C07K14/47, A61K38/00|
|Cooperative Classification||A01K2217/05, C07K14/4733, A61K38/00, C07K14/474, C07K2319/00|
|European Classification||C07K14/47A27, C07K14/47A22|