2002, Número 6
<< Anterior Siguiente >>
Gac Med Mex 2002; 138 (6)
Neogénesis y regeneración de las células Β pancreáticas
Haro-Hernández R, Méndez JD
Idioma: Español
Referencias bibliográficas: 73
Paginas: 557-564
Archivo PDF: 52.46 Kb.
RESUMEN
Objetivo: Revisar la literatura biomédica acerca de la neogénesis y regeneración de las células Β pancreáticas con énfasis en la regulación de estos procesos.
Diseño: Se localizaron los artículos más relevantes sobre el tema mediante una búsqueda en la base de datos MEDLINE que comprendió de 1990 a 2000.
Resultados: Los datos reportados en la literatura demuestran que la diferenciación de los islotes de Langerhans a partir de conductos pancreáticos pequeños durante la formación del páncreas, en condiciones normales no continúa. Sin embargo, se ha determinado que en ciertos modelos experimentales in vivo la formación de nuevas células Β puede ocurrir por neogénesis, para esto es muy importante la expresión del gen Pax 4. El proceso de regeneración de células Β es inducido por varias sustancias, entre ellas glucosa, varias hormonas y ciertos factores de crecimiento.
Conclusiones: Los mejores resultados observados con las sustancias que estimulan el proceso de regeneración de las células Β se han obtenido empleando concentraciones que rebasan los niveles fisiológicos, por lo que su posible importancia terapéutica no es muy clara. Sin embargo, existen posibilidades reales de que la proteína Reg pudiera, en el futuro, tener aplicación clínica.
REFERENCIAS (EN ESTE ARTÍCULO)
1. Lacy PE. The pancreatic b-cell. Structure and function. N Engl J Med 1967;276:187-195.
2. Reaven GM. Pathophysiology of insulin resistance in human disease. Physiol Rev 1995;75:473-486.
3. Ferrannini E. Insulin resistance versus insulin deficiency in non-insulin dependent diabetes mellitus: problems and prospects. Endocr Rev 1998;19:477-490.
4. Atkinson MA, Maclaren NK. The pathogenesis of insulin-dependent diabetes mellitus. N Engl J Med 1996;331: 1428-1436.
5. Hellerström C, Swenne I. Functional maturation and proliferation of fetal pancreatic b-cells. Diabetes 1991;40 (Suppl 2):89-93.
6. Sjöholm, A. Role of polyamines in the regulation of proliferation and hormone production by insulin-secreting cells. Am J Physiol 1993;264:C501-C518.
7. Bach J-F. Insulin-dependent diabetes mellitus as an autoimmune disease. Endocr Rev 1994;15:516-542.
8. Logothetopoulos J. Islet regeneration and neogenesis. In: Freinkel N, editor. Handbook of physiology: Endocrinology. Vol. 1, Baltimore MD, USA: Weverly Press; 1972. p. 67-76.
9. Sjöholm Á. Diabetes mellitus and impaired pancreatic b-cell proliferation. J Int Med 1996;239:211-220.
Tanigawa K, Nakamura S, Kawaguchi M, Xu G, Kin S, Tamura K. Effect of aging on b-cell function and replication in rat pancreas after 90% pancreatectomy. Pancreas 1997;15:53-59.
Hardikar AA, Karandikar MS, Bhonde RR. Effect of partial pancreatectomy on diabetic status in BALB/c mice. J Endocrinol 1999;162:189-195.
Davidson PM, Campbell LL, Oxbrow L, Hutson JM, Harrison LC. Pancreatic b-cell proliferation in rabbits demonstrated by bromodeoxyuridine labeling. Pancreas 1989;4:594-600.
Gu D, Sarvetnik N. Epithelial cell proliferation and islet neogenesis in INF-Y transgenic mice. Development 1993; 118:33-46.
Sjüholm A. Glucose stimulates islet b-cell mitogenesis through GTP-binding proteins and protein kinase C-dependent mechanisms. Diabetes 1997;46:1141-1147.
Otonkoski T, Mally MI, Hayek A. Opposite effects of b-cell differentiation and growth on Reg expression in human fetal pancreatic cells. Diabetes 1994;43:1164-1166.
Tanabe K, Okuya S, Tanizawa Y, Matsutani A, Yoshimoto O. Leptin induces proliferation of pancreatic b-cell line MIN6 through activation of mitogen-activated protein kinase. Biochem Biophys Res Commun 1997;241:765-678.
Defazio A, Leary JA, Hedley DW, Tattersali MHN. Immunohistochemical detection of proliferating cells in vivo. J Histochem Cytochem 1987;35:571-577.
Iatropoulos MG, Williams GM. Proliferation markers. Exp Toxicol Pathol 1996;48:175-181.
Rosenherg L. Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model. Microsc Res Tech 1998;43:337-346.
Debas HT. Molecular insights into the development of the pancreas. Am J Surg 1997;174:227-231.
Rosenberg L, Vinik AI. Trophic stimulation of the ductular-islet cell axis: a new approach to the treatment of diabetes. Adv Exp Med Biol 1992;321:95-104.
Sarvetnik N, Liggitt D, Pitts SL, Hansen SE, Stewart TA. Insulin-dependent diabetes mellitus induced in transgenic mice by ectopic expression of class 11 MHC and interferon-X. Cell 1998;52:773-782.
Sander M, German MS. The b-cell transcription factors and development of the pancreas. J Mol Med 1997;75:327-340.
Sosa-Pineda B, Chowdhury K, Torres M, Oliver G, Gruss P. The Pax4 gene is essential for differentiation of insulin-producing P-cells in the mammalian pancreas. Nature 1997;386:399-402.
Kritzik MR, Krahl T, Good A, Krakowsky M, St.-Onge L, Gruss P, Wright C, Sarvetnik N. Transcription factor expression during pancreatic islet regeneration. Mol Cell Endocrinol 2000;164:99-107.
Bonner-Weir S. Regulation of pancreatic b-cell mass in vivo. Recent Prog Horm Res 1994;49:91-104.
Bonner-Weir S, Smith FE. Islet cell growth and the growth factors involved. Trends Endocrinol Metabol 1994;5:60-64.
Kasai M, lkeuchi M. Regulation of pancreatic B-cell replication by glucose and some other substances. Biomed Res 1982;3:688-692.
Bonner-Weir S, Deery D, Leahy JL, Weir GC. Compensatory growth of pancreatic b-cells in adult rats after short-term glucose infusion. Diabetes 1989;38:49-53.
King DL, Kitchen KC, Chick WL. Pancreatic b-cell replication: relation to insulin secretion. Endocrinology 1978;103:321-327.
Sweene I. The role of glucose in the in vitro regulation of cell cycle kinetics and proliferation in fetal b-cells. Diabetes 1982;31:754-760.
Hostens K, Ling Z, Van Schravendijk C, Pipeleers D. Prolonged exposure of human cells to high glucose increases their release of proinsulin during acute stimulation with glucose or arginine. J Clin Endocrinol Metabol 1999;84:1386-1390.
Klüppel G, Lühr M, Hablich K, Oberholzer M, Heitz PU. Islet pathology and pathogenesis of type 1 and type 2 diabetes mellitus revisited. Surv Synth Pathol Res 1985;4:110-125.
Popiela H, Moore W. Tolbutamide stimulates proliferation of pancreatic b-cells in culture. Pancreas 1991;6:664-668.
Guiot Y, Henquin J-C, Rahier J. Effects of glibenclamide on pancreatic b-cell proliferation in vivo. Eur J Pharmacol 1994;261:157-161.
Elmquist JK, Elias CF, Saper CB. From lesions to leptin: hypothalamic control of food intake and body weight. Neuron 1999;22:221-232.
Islam MS, Morton NM, Hansson A, Emilsson V. Rat insulinoma derived pancreatic beta-cells express a functional leptin receptor that mediates a proliferative response. Biochem Biophys Res Commun 1997;238:851-855.
Ferrannini E. Insulin resistance versus insulin deficiency in non-insulin-dependent diabetes mellitus: problems and prospects. Endocr Rev 1998;19:477-490.
Yates JA, DeFronzo RA. Metabolic disorders. In: Stein JH, editors. Internal Medicine: diagnosis and therapy. USA: Appleton & Lange; 1993. p. 497-535.
Bengtsoon BA. The consequences of growth hormone deficiency in adults. Acta Endocrinol 1993;128(Suppl 2):2-5.
Sweene I, Hill DJ, Strain AJ, Milner RDG. Growth hormone regulation of somatomedin C/insulin-like growth factor 1 production and DNA replication in fetal rat islets in tissue culture. Diabetes 1987;36:288-294.
Billestrup N, Nielsen JH. The stimulatory effect of growth hormone, prolactin and placental lactogen on b-cell proliferation is not mediated by insulin-like growth factor. Endocrinology 1991;129:883-888.
Smith FE, Rosen KM, Villa-Komaroff L, Weir GC, Bonner-Weir S. Enhanced insulin-like growth factor 1 gene expression in the regenerating rat pancreas. Proc Natl Acad Sci USA 1991;88:6152-6156.
Cousin SP, Hügl SR, Myers MG, White MF, Reifier-Miller A, Rhodes CJ. Stimulation of pancreatic b-cell proliferation by growth hormone in glucose-dependent: signal transduction via Janus kinase 2 (JAK2)/signal transduction and activator of transcription 5 (STAT5) with no crosstalk to insulin receptor substrate-mediated mitogenic signaling. Biochem J 1999;344:649-658.
Nielsen JH. Effects of growth hormone, prolactin, and placental lactogen on insulin content and release, and deoxyribonucleic acid synthesis in cultured pancreatic islets. Endocrinology 1982;110:600-606.
Brelje CT, Scharp DW, Lacy PE, Ogren L, Talamantes F, Robertson M, Friesen HG, Sorenson RL. Effect of homologous placental lactogens, prolactins, and growth hormones on islet b-cell division and insulin secretion in rat, mouse, and human islets: implication for placental lactogen regulation of islet function during pregnancy. Endocrinology 1993; 132:879-887.
Moldrup A, Billestrup N, Nieisen JH. Rat insulinoma cells express both a 115-kDa growth hormone receptor and a 95-kDa prolactin receptor structurally related to the hepatic receptors. J Biol Chem 1990;265:8686-8690.
Okamoto H. New aspects to the functioning and regeneration of pancreatic b-cells. Adv Exp Med Biol 1997;426:301-311.
Yonemura Y, Takashima T, Matsuda Y, Miwa K, Sugiyama K, Miyazaki 1, Yamamoto H, Okamoto H. Amelioration of diabetes in partially depancreatized rats by poly (ADPribose) synthetase inhibitors- evidence of islet b-cell regeneration. Diabetes 1984;33:401-404.
Yonemura Y, Takashima T, Matsuda Y, Miwa K, Sugiyama K, Miyazaki 1, Yamamoto H, Okamoto H. Induction of islet b-cell regeneration in partially pancreatectomized rats by poly (ADP-ribose) synthetase inhibitors. Int J Pancreatol 1988;3:73-82.
Terazono K, Yamamoto H, Takasawa S, Shiga K, Yonemura Y, Tochino Y, Okamoto H. A novel gene activated in regenerating islets. J Biol Chem 1988;263:2111-2114.
Unno M, ltoh T, Watanabe T, Miyashita H, Moriizumi S, Teraoka H, Yonekura H, Okamoto H. Islet cell regeneration and Reg genes. Adv Exp Med Biol 1992;321:95-112.
Okamoto H. The Reg gene family and Reg proteins: with special attention to the regeneration of pancreatic beta-cells. J Hepato-Biliary-Pancreatic Surg 1999;6:254-262.
Anastasi E, Ponte E, Gradini R, Bulotta A, Sale P, Tiberti C, Okamoto H, Dotta F, Di Mario U. Expression of Reg and cytokeratin 20 during ductal cell differentiation and proliferation in a mouse model of autoimmune diabetes. Eur J Endocrinol 1999;141:644-652.
Watanabe T, Yonekura H, Terazono K, Yamamoto H, Okamoto H. Complete nucleotide sequence of human reg gene and its expression in normal and tumoral tissue. J Biol Chem 1990;265:3589-3592.
Miyaura C, Chen L, Appel M, Alam T, Inman L, Hughes SD, Milburn JL, Unger RH, Newgard CB. Expression of reg/PSP, a pancreatic exocrine gene: relationship to changes in islet b-cell mass. Mol Endocrinol 1991;5:226-234.
Fukui H, Kinoshita Y, Maekawa,T, Okada A, Waki S, Hassan S, Okamoto H, Chiba T. Regeneration gene protein may mediate gastric mucosal proliferation induced by hypergastrinemia in rats. Gastroenterology 1998;115:1 483-1493.
Salata R, Klein I. Effects of lithium on the endocrine system: a review. J Lab Clin Med 1987-110:130-142.
Sjöholm A, Welsh N, Rellerstrüm C. Lithium increases DNA replication, polyamine content, and insulin secretion by rat pancreatic b-cells. Am J Physiol 1992;262:C391-C395.
Pegg AE. Recent advances in the biochemistry of polyamines in eukaryotes. Biochem J 1986;234: 249-262.
Marton LJ, Pegg AE. Polyamines as targets for therapeutic intervention. Annu Rev Pharmacol Toxicol 1995;35:55-91.
Floyd JC, Fajans SS, Conn JW, Knopf RF, Rull J. Stimulation of insulin secretion by aminoacids. J Clin Invest 1966;45:1487-1502.
Edgard P, Rabinowitz D, Merimee TJ. Effects of aminoacids on insulin release from excised rabbit pancreas. Endocrinology 1969;84:835-843.
Hougaard, DM, Nielsen JH, Larson LI. Localization and biosynthesis of polyamines in insulin-producing cells. Biochem J 1986;238:43-47.
Smith PA, Sakura H, Coles B, Gummerson N, Proks P, Ashcroft FM. Electrogenic arginine transport mediates stimulus-secretion coupling in mouse pancreatic b-cells. J Physiol 1997;499:625-635.
Thams P, Capito K. L-arginine stimulation of glucose-induced insulin secretion through membrane depolarization and independent of nitric oxide. Eur J Endocrinol 1999; 140:87-93.
Sjüholm A, Weish N, Sandler S, Hellerstrüm C. Role of polyamines in mitogenic and secretory responses of pancreatic b-cells to growth factors. Am J Physiol 1990;259:C828C833.
Sjöholm A. Intracellular signal transduction pathways that control pancreatic P-cell proliferation. FEBS Lett 1992;311:85-90.
Welsh N, Sjöholm A. Polyamines and insulin production in isolated mouse pancreatic islets. Biochem J 1988;252: 701-707.
Welsh N. A role for polyamines in glucose-stimulated insulin-gene expression. Biochem J 1990;271:393-397.
Méndez JD, Zarzoza E. Inhibition of platelet aggregation by L-arginine and polyamines in alloxan treated rats. Biochem Mol Biol Int 1997;43:311-318.
Méndez JD, Palomar-Morales M. Prevention by L-arginine and polyamines of delayed development and embryotoxicity caused by chemically induced diabetes in rats. Reprod Toxicol 1999;13:501-509.
Méndez JD, Balderas F. Regulation of hyperglucemia and dyslipidemia by exogenous L-arginine in diabetic rats. Biochimie 2001;83(5):453-458.