Differentiation of new insulin-producing cells is induced by injury in adult pancreatic islets.

The ability of the adult pancreas to generate new insulin (beta) cells has been controversial because of difficulties in unequivocally identifying the precursor population. We recently determined that beta cells were generated during development from precursors that expressed the homeodomain-containing transcription factor pancreas duodenum homeobox gene-1 (PDX-1). To investigate whether PDX-1+ stem cells are present in adult pancreas, we examined two animal models of diabetes. One model was produced by injecting adult mice with streptozotocin (SZ), a toxin that produces hyperglycemia due to rapid and massive beta cell death. After SZ-mediated elimination of existing IN+/PDX-1+ cells, a population of somatostatin (SOM)+/PDX-1+ cells, a cell type thought to represent an embryonic islet precursor cell, appeared in islets. The appearance of SOM+/PDX-1+ cells was followed in time by the differentiation to SOM+/IN+/PDX-1+ cells. SOM+/PDX-1+ cells also appeared in islets of nonobese diabetic mice, a strain of mice in which beta cell destruction is immune-mediated. Our findings establish the existence of PDX-1+ beta cell precursors in the adult pancreas and indicate that their differentiation is induced by islet injury.

[1]  B. Hogan,et al.  PDX-1 is required for pancreatic outgrowth and differentiation of the rostral duodenum. , 1996, Development.

[2]  C. Fathman,et al.  Monoclonal T cells identified in early NOD islet infiltrates. , 1996, Immunity.

[3]  J. Merrill,et al.  Interactions of the nervous and immune systems in development, normal brain homeostasis, and disease 1 , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[4]  R. Stein,et al.  Expression of murine STF-1, a putative insulin gene transcription factor, in beta cells of pancreas, duodenal epithelium and pancreatic exocrine and endocrine progenitors during ontogeny. , 1995, Development.

[5]  L. Olson,et al.  Erratum: Reduction of insulin gene transcription in HIT-T15 β cells chronically exposed to a supraphysiologic glucose concentration is associated with loss of STF-1 transcription factor expression (Cell (September 26, 1995) 92:20 (9127-9131)) , 1995 .

[6]  M. Montminy,et al.  Insulin expression in pancreatic islet cells relies on cooperative interactions between the helix loop helix factor E47 and the homeobox factor STF-1. , 1994, Molecular endocrinology.

[7]  O. Madsen,et al.  Transcriptional regulation of the human insulin gene is dependent on the homeodomain protein STF1/IPF1 acting through the CT boxes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[8]  H. Edlund,et al.  Insulin-promoter-factor 1 is required for pancreas development in mice , 1994, Nature.

[9]  N. Sarvetnick,et al.  Transitional cells in the regenerating pancreas. , 1994, Development.

[10]  R. Stein,et al.  XIHbox 8, an endoderm-specific Xenopus homeodomain protein, is closely related to a mammalian insulin gene transcription factor. , 1994, Molecular endocrinology.

[11]  J. Habener,et al.  IDX‐1: a new homeodomain transcription factor expressed in rat pancreatic islets and duodenum that transactivates the somatostatin gene. , 1994, The EMBO journal.

[12]  A. Leiter,et al.  Expression of peptide YY in all four islet cell types in the developing mouse pancreas suggests a common peptide YY-producing progenitor. , 1994, Development.

[13]  J. Parsons,et al.  Regulation of islet beta-cell proliferation by prolactin in rat islets. , 1994, Diabetes.

[14]  L. Baxter,et al.  A Second Pathway for Regeneration of Adult Exocrine and Endocrine Pancreas: A Possible Recapitulation of Embryonic Development , 1993, Diabetes.

[15]  H. Ohlsson,et al.  IPF1, a homeodomain‐containing transactivator of the insulin gene. , 1993, The EMBO journal.

[16]  M. Montminy,et al.  Characterization of somatostatin transactivating factor-1, a novel homeobox factor that stimulates somatostatin expression in pancreatic islet cells. , 1993, Molecular endocrinology.

[17]  D. Hanahan,et al.  Precursor cells of mouse endocrine pancreas coexpress insulin, glucagon and the neuronal proteins tyrosine hydroxylase and neuropeptide Y, but not pancreatic polypeptide. , 1993, Development.

[18]  N. Sarvetnick,et al.  Epithelial cell proliferation and islet neogenesis in IFN-g transgenic mice. , 1993, Development.

[19]  O. Korsgren,et al.  Ultrastructural studies of the ontogeny of fetal human and porcine endocrine pancreas, with special reference to colocalization of the four major islet hormones. , 1992, Developmental biology.

[20]  W. J. Visser,et al.  The midgestational human fetal pancreas contains cells coexpressing islet hormones. , 1992, Developmental biology.

[21]  L. Orci,et al.  Embryogenesis of the murine endocrine pancreas; early expression of pancreatic polypeptide gene. , 1991, Development.

[22]  M. Welsh,et al.  Exposure of pancreatic islets to different alkylating agents decreases mitochondrial DNA content but only streptozotocin induces long-lasting functional impairment of B-cells. , 1991, Biochemical pharmacology.

[23]  M. Atkinson,et al.  Insulitis and Diabetes in NOD Mice Reduced by Prophylactic Insulin Therapy , 1990, Diabetes.

[24]  A. Vinik,et al.  Induction of endocrine cell differentiation: a new approach to management of diabetes. , 1989, The Journal of laboratory and clinical medicine.

[25]  P. Schnegelsberg,et al.  XlHbox 8: a novel Xenopus homeo protein restricted to a narrow band of endoderm. , 1989, Development.

[26]  Robert L. Hazelwood,et al.  The endocrine pancreas , 1989 .

[27]  D. Hanahan,et al.  Hybrid insulin genes reveal a developmental lineage for pancreatic endocrine cells and imply a relationship with neurons , 1988, Cell.

[28]  D. Hanahan,et al.  Proliferation, senescence, and neoplastic progression of β cells in hyperplasic pancreatic islets , 1988, Cell.

[29]  G. Teitelman,et al.  Cell lineage analysis of pancreatic islet development: glucagon and insulin cells arise from catecholaminergic precursors present in the pancreatic duct. , 1987, Developmental biology.

[30]  C. Nathan,et al.  Secretory products of macrophages. , 1987, The Journal of clinical investigation.

[31]  P. Lecompte,et al.  The Pathology of Type I (Juvenile) Diabetes , 1985 .

[32]  S. Bonner-Weir,et al.  Partial pancreatectomy in the rat and subsequent defect in glucose-induced insulin release. , 1983, The Journal of clinical investigation.

[33]  C. Rozé,et al.  Ultrastructural study of pancreatic B cell regeneration in newborn rats after destruction by streptozotocin , 1982, Virchows Archiv. B, Cell pathology including molecular pathology.

[34]  L. Larsson A novel immunocytochemical model system for specificity and sensitivity screening of antisera against multiple antigens. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[35]  S. Bonner-Weir,et al.  Responses of Neonatal Rat Islets to Streptozotocin: Limited B-Cell Regeneration and Hyperglycemia , 1981, Diabetes.

[36]  E. Weibel Practical methods for biological morphometry , 1979 .

[37]  M. Maxwell Two rapid and simple methods used for the removal of resins from 1.0 μm thick epoxy sections , 1978, Journal of microscopy.

[38]  I. Swenne,et al.  Growth Pattern of Pancreatic Islets in Animals , 1977 .

[39]  E. Arquilla,et al.  The Diabetic Pancreas , 1977, Springer US.

[40]  A. Rossini,et al.  Streptozotocin-induced pancreatic insulitis: new model of diabetes mellitus. , 1976, Science.

[41]  A. Andersson,et al.  Regeneration of islet cells. , 1976, Acta endocrinologica. Supplementum.

[42]  M. Ellenberg,et al.  Diabetes mellitus: theory and practice , 1970 .

[43]  A. Renold,et al.  Diabetogenic action of streptozotocin: relationship of dose to metabolic response. , 1969, The Journal of clinical investigation.

[44]  G. Brosky,et al.  Streptozotocin Diabetes in the Mouse and Guinea Pig , 1969, Diabetes.

[45]  L. Orci,et al.  Studies of the Diabetogenic Action of Streptozotocin.∗ , 1967, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[46]  A. W. Rogers Techniques of autoradiography , 1967 .

[47]  G de J Lee,et al.  Handbook of Physiology Section 2. , 1965 .

[48]  W. Schweisheimer [DIABETES IN ANIMALS]. , 1964, Medizinische Klinik.