Conclusion
Collectively, these studies provide an insight into some of the dynamic factors that modulate the CGA expression, posttranslational processing and secretion during ontogeny and in the mature neuroendocrine cell population of the GEP system. The dynamic changes probably reflect the differential expression of proteolytic enzymes that take part in the processing of CGA. Understanding the mechanisms that control the expression and processing of CGA-derived peptides will help us elucidate their functional significance.
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References
Arden, S.D., Rutherford, N.G., Guest, P.C., Curry W.J., Bailyes, E.M., Johnston, C.F., and Hutton, J.C., 1994, The post-translational processing of chromogranin A in the pancreatic islet: involvement of the eukaryote subtilisin PC2. Biochem. J. 298:521–528.
Barkatullah, S.C., Curry, W.J., Johnston, C.F., Hutton, J.C., and Buchanan, K.D., 1997, Ontogenetic expression of chromogranin A and its derived peptides, WE-14 and pancreastatin, in the rat neuroendocrine system. Histochem. Cell. Biol. 107:251–257.
Bretherton-Watt, D., Ghatei, M.A., Bishop, A.E., Facer, P., Fahey, M., Hedges, M., Williams, G., Valentino, K.L., Tatemoto, K., Roth, K., Polak, J.M., and Bloom, S.R., 1988, Pancreastatin distribution and plasma levels in the pig. Peptides 9:1005–1014.
Capella, C., Finzi, G., Cornaggia, M., Usellini, L., Luinetti, O., Buffa, R., Solcia, E., Ultrastructural typing of gastric endocrine cells. In The Stomach as an Endocrine Organ (R. Håkanson and F. Sundler, eds.), FemstrÖm Found. Series, Symp. no. 15, Elsevier Science, Amsterdam, 1991, pp. 27–51.
Curry, W.J., Johnston, C.F., Hutton, J.C., Arden, S.D., Rutherford, N.G., Shaw, C., and Buchanan, K.D., 1991, The tissue distribution of rat chromogranin A-derived peptides: evidence for differential tissue processing from sequence specific antisera. Histochem. 96:531–538.
Curry, W.J., Johnston, C.F., Shaw, C., and Buchanan, K.D., 1990, Distribution and partial characterisation of immunoreactivity to the putative C-terminus of rat pancreastatin. Regul. Pept., 30:207–219.
Curry, W.J., Johnston C.F., and Buchanan, K.D., 1994, Peptides and neuropeptides of the pancreatic islets. In Frontiers of insulin secretion and pancreatic B cell research (P.R. Flatt and S. Lenzen, eds) pp 40/1–40/8. Smith-Gordon Ltd, London.
Curry, W.J., Johnston, C.F., Shaw, C., and Buchanan, K.D., 1997, Colocalization of WE-14 immunostaining with the classical islet hormones in the porcine pancreas. Adv. Exp. Med. Biol. 426:139–144.
Curry, W.J., Shaw, C., Johnston, C.F., Thim, L., and Buchanan, K.D., 1992, Isolation and primary structure of a novel chromogranin A derived peptide, WE-14, from a midgut carcinoid tumour. FEBSLett 30:319–321.
Dimaline, R., Evans, D., Forster, E.R., Sandvik, A.K., and Dockray, G.J., 1993, Control of gastric corpus chromogranin A messenger RNA abundance in the rat. Am. J. Physiol. 264:G583–588.
Dubois, P.M., 1989 Ontogeny ofthe endocrine pancreas. Horm. Res. 32:53–60.
Gittes, G.K., and Rutter, W.J., 1992, Onset of cell-specific gene expression in the developing mousepancreas. Proc.Natl. Acad. Sci. USA 89:1128–1132.
Håkanson, R., Ding, X.Q., Norlén, P., and Chen, D., 1995, Circulating pancreastatin in the rat is a marker for the enterochromaffin-like cells. Gastroenterology, 108: 1445–1456.
Hutton, J.C., Davidson, H.W., Grimaldi, K.A., and Peshavaria, M., 1987, Biosynthesis of betagranin in pancreatic b-cells. Biochem. J. 244:449–456.
Hutton, J.C., Nielsen, E., and Kastem, W., 1988, The molecular cloning of the chromogranin A-like precursor of b-granin and pancreastatin from the endocrine pancreas. FEBS Letters 236:269–274.
Hutton, J.C., Penn, E.J., and Peshavaria, M.., 1982, Isolation and characterization of insulin secretory granules from rat islet cell tumour. Diabetologia 23:365–373.
Iacangelo, A.L., and Eiden, L.E., 1995, Chromogranin A: current status as a precursor for bioactive peptides and a granulogenic/sorting factor in the regulated secretory pathway. Regul. Pept. 58:65–88.
Iacangelo, A.L., Affolter, H-U., Eiden, L.E., Herbert, E., and Grimes, M., 1986, Bovine chromogranin A sequence and distribution of its messanger RNA in endocrine tissues. Nature 323:82–86.
Jin, S-L., C., Hynes, M.A., Simmons, J.G., Lauder, J.M., and Lund, P.K., 1992, Ontogeny of glucagon messanger RNA in the rat pancreas. Histochemistry 97:431–438.
Kimura, K., Chen, D., Lindstrom, E., Zhao, C.M., and Håknson, R., 1997, Evidence that rat stomach ECL cells represent the main source of circulating pancreastatin. Regul. Pept. 68:177–80.
Le Douarin N., 1982, The Neural Crest. Cambridge University Press.
Marcinkiewicz, M., Ramla, D., Seidah, N.G., and Chrétien, M., 1994, Developmental expression of the prohormone convertases PCl and PC2 in mouse pancreatic islets. Endocrinol. 135:1651–1660.
Norlén, P., Curry, W.J., Chen, D., Zhao, C-M., Johnston, C.F., and Håkanson, R., 1997, Expression of the chromogranin A-derived peptides pancreastatin and WE14 in rat stomach ECL cells. Regul. Pept. 70:121–133.
Ponder, B.A.J., Schmidt, G.H., Wilkinson, M.M., Wood, M.J., Monk, M., and Reid, A., 1985, Derivation ofmouse intestinal crypts from single progenitor cells. Nature 313:689–691.
Portela-Gomes, G.M., Stridsberg, M., Johansson, H., and Grimelius, L., 1997, Complex colocalisation of chromogranins and neurohormones in the human gastrointestinal tract. J. Histochem. Cytochem. 45:815–822.
Rutter, W.J., 1980, The development of the endocrine and exocrine pancreas. In: The pancreas (P.J. Fitzgerald, and A.B. Morrison, eds.), Williams and Wilkins, Batimore. pp30–38.
Sundler, F., 1998, Ontogeny ofECL cells in the rat. Yale. J. Biol. Med. 71:155–61.
Sundler, F., and Håkanson, R., 1984, Gastro-entero-pancreatic endocrine cells in higher mammals, with special reference to their ontogeny in the pig. In: Evolution and tumour pathology of the neuroendocrine system. (S. Falkmer, R. Håkanson and F. Sundler, eds.) Elsevier Science. pp111–135.
Sundler, F., and Håkanson, R., 1991, Gastric endocrine cell typing at the light microscopic level. In, The Stomach as an Endocrine Organ (R. Håkanson and F. Sundler, eds.), Fernstrom Found. Series, Symp. no. 15, Elsevier Science, Amsterdam, pp9–26.
Tatemoto, K., Efendic, S., Mutt, V., Makk, G., Feistner, J., and Barchas, J.D., 1986, Pancreastatin, a novel pancreatic peptide that inhibits insulin secretion. Nature 324:476–478.
Wiedenmann, B., and Huttner, W.B., 1989, Synaptophysin and chromogranins/secretogranins-widespread constituents of distinct types of neuroendocrine vesicles and new tools in tumour diagnosis. Virchows. Archiv. B. Cell. Pathol. 58:95–121.
Yoshinari, M., and Daikoku, S., 1982, Ontogenetic appearance of immunoreactive endocrine cells in rat pancreatic islets. Anat. Embryol. 165:63–70.
Zabel, M., Surdyk-Zasada, J., Lesisz, I., Jagoda, E., Wysocka, T., Seidel, J.,and Grezeszkowiak, J., 1994, Immunocytochemical studies on pancreatic endocrine cells at early stages of development of the pig. FoliaHistochemica et Cytobiologica 32:181–185.
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Curry, W.J., Norlén, P., Barkatullah, S.C., Johnston, C.F., Håkanson, R., Hutton, J.C. (2002). Chromogranin A and Its Derived Peptides in the Rat and Procine Gastro-Entero-Pancreatic System. In: Helle, K.B., Aunis, D. (eds) Chromogranins. Advances in Experimental Medicine and Biology, vol 482. Springer, Boston, MA. https://doi.org/10.1007/0-306-46837-9_16
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