Cholecystokinin-Induced Inhibition of Endocytosis of Receptor-Bound Substance P in Pancreatic Acinar Cells

References

• Sjödin L. Binding and internalization of 125I-Bolton-Hunter-Substance P by pancreatic acinar cells. Biochem. Biophys. Res. Comm. 1984; 124: 578–584
   Google Scholar
• Sjödin L., Brodin E., Nilsson G., Conlon T. P. Interaction of substance P with dispersed pancreatic acinar cells from the guinea pig. Binding of radioiodinated peptide. Acta Physiol. Scand. 1980; 109: 97–105
   PubMedGoogle Scholar
• Sjödin L., Brodin E., Srivastava G. Interaction of substance P with dispersed pancreatic acinar cells from the guinea pig. Relationships between structure, binding and biological activity. Acta Physiol. Scand. 1984; 120: 21–26
   Google Scholar
• Sjödin L., Conlon T. P., Gustavson C., Uddholm K. Interaction of substance P with dispersed pancreatic acinar cells from the guinea pig. Stimulation of calcium outflux, accumulation of cyclic GMP and amylase release. Acta Physiol. Scand. 1980; 109: 107–110
   PubMedGoogle Scholar
• Sjödin L., Dahlén H. G., Lund P. E., Gylfe E. Stimulation of pancreatic amylase release is associated with a parallel sustained increase of cytoplasmic calcium. Regulatory Peptides 1990; 30: 239–253
   PubMedGoogle Scholar
• Sjödin L. Cholecystokinin inhibits binding of substance P to pancreatic acinar cells. Acta Physiol. Scand. 1985; 124: 471–474
   Google Scholar
• Logsdon C. D., Williams J. A. Epidermal growth factor: intracellular Ca2+ inhibits its association with pancreatic acini and A431 cells. FEES lett. 1983; 164: 335–339
   Google Scholar
• Potau N., Mössner J., Williams J. A., Goldfine I. D. Cholecystokinin and insulin regulate insulin-like growth factor II binding to pancreatic receptors; evidence of a role for intracellular calcium. Biochem. Biophys. Res. Comm. 1984; 119: 359–364
   Google Scholar
• Okabayashi Y., Otsuki M., Nakamura T., Koide M., Hasegawa H., Okutani T., Kido Y. Regulatory effect of cholecystokinin on subsequent insulin binding to pancreatic acini. Am. J. Physiol. 1990; 258: E562–E568
   Google Scholar
• Esteve J. P., Susini C., Vaysse N., Antoniotti H., Wunsch E., Berthon G., Ribet A. Binding of somatostatin to pancreatic acinar cells. Am. J. Physiol. 1984; 247: G62–G69
   Google Scholar
• Sakamoto C., Goldfine I. D., Williams J. A. The somatostatin receptor on isolated pancreatic acinar cell plasma membranes. J. Biol. Chem. 1984; 259: 9623–9627
   PubMedGoogle Scholar
• Younes M., Wank S. A., Vinayek R., Jensen R. T., Gardner J. D. Regulation of bombesin receptors on pancreatic acini by cholecystokinin. Am. J. Physiol. 1989; 256: G291–G298
   Google Scholar
• Delhaye M., Taton G., Poirier G., Larose L., St James S., Morisset J. Modulation of rat pancreatic muscarinic cholinergic receptors by caerulein. Biochem. Pharmacol. 1985; 34: 1057–1063
   PubMedGoogle Scholar
• Bruzzone R., Pozzan T., Wollheim C. B. Caerulein and carbamylcholine stimulate pancreatic amylase release at resting cytosolic free Ca2+. Biochem. J. 1986; 235: 139–143
   PubMedGoogle Scholar
• Ochs D. L., Korenbrot J. I., Williams J. A. Relationship between free cytosolic calcium and amylase release by pancreatic acini. Am. J. Physiol. 1985; 249: G389–G398
   Google Scholar
• Pandol S. J., Schoeffield M. S., Sachs G., Muallem S. Role of free cytosolic calcium in secretagogue stimulated amylase release from dispersed acini from guinea pig pancreas. J. Biol. Chem. 1985; 260: 10081–10086
   Google Scholar
• Pandol S. J., Thomas M. W., Schoeffield M. S., Sachs G., Muallem S. Role of calcium in chole-cystokinin-stimulated phosphoinositide breakdown in exocrine pancreas. Am. J. Physiol. 1985; 248: G551–G560
   Google Scholar
• Streb H., Heslop J. P., Irvine R. F., Schultz I., Berridge M. J. Relationship between secretagogue-induced Ca2+ release and inositol polyphosphate production in permeabilized pancreatic acinar cells. J. Biol. Chem. 1985; 260: 7309–7315
   PubMed Web of Science ®Google Scholar
• Reed P. W., Lardy H. A. A23187: a divalent cation ionophore. J. Biol. Chem. 1972; 247: 6970–6977
   PubMed Web of Science ®Google Scholar
• Sjödin L. Binding of substance P to pancreatic acinar cells. Inhibition by ionophore A23187. Proc. of Xth Int. Congress of Pharmacol. Abstract, Sidney, 1987
   Google Scholar
• Amsterdam A., Jamieson J. D. Structural and functional characterization of isolated pancreatic exocrine cells. Proc. Natl. Acad. Sci. (U. S. A.) 1972; 69: 3028–3032
   PubMed Web of Science ®Google Scholar
• Lowry O. M., Rosebrough N. J., Farr A. L., Randall R. J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 1951; 193: 265–275
   PubMed Web of Science ®Google Scholar
• Chance B., Legallais V., Sorge J., Graham N. A versatile time-sharing multichannel spectrophotometer, reflectometer and fluorometer. Anal. Biochem. 1975; 66: 498–514
   PubMed Web of Science ®Google Scholar
• Gylfe E. Glucose-induced early changes in cytoplasmic calcium of pancreatic B-cells studied with time-sharing dual-wavelength fluorometry. J. Biol. Chem. 1988; 263: 5044–5048
   PubMed Web of Science ®Google Scholar
• Munson P. J., Rodbard D. Ligand: A versatile computerized approach for characterization of ligand-binding systems. Anal. Biochem. 1980; 107: 220–239
   PubMed Web of Science ®Google Scholar
• Anastasi A., Erspamer V., Endean R. Isolation and amino acid sequence of caerulein, the active decapeptide of the skin of Hyla caerulea. Arch. Biochem. Biophys. 1968; 125: 57–68
   PubMed Web of Science ®Google Scholar
• Sankaran H., Goldfine I. D., Deveney C. W., Wong K. Y., Williams J. A. Binding of cholecystokinin to high affinity receptors on isolated rat pancreatic acini. J. Biol. Chem. 1990; 255: 1849–1853
   Google Scholar
• Sankaran H., Goldfine I. D., Bailey A., Licko V., Williams J. A. Relationship of cholecystokinin receptor binding to regulation of biological functions in pancreatic acini. Am. J. Physiol. 1982; 242: G250–G257
   PubMed Web of Science ®Google Scholar
• Gardner J. D., Jensen R. T. Secretagogue receptors on pancreatic acinar cells. Physiology of the gastrointestinal tract2nd edition, L. R. Johnson. Raven Press, New York 1987; 1109–1127
   Google Scholar
• Williams J. A., Bailey A. C., Roach E. Temperature dependence of high-affinity CCK receptor binding and CCK internalization in rat pancreatic acini. Am. J. Physiol. 1988; 254: G513–G521
   Google Scholar
• Carpenter G., Cohen S. 125I-labeled human epidermal growth factor. J. Cell. Biol. 1976; 71: 159–171
   PubMed Web of Science ®Google Scholar
• Korc M., Matrisian L. M., Magun B. E. Cytosolic calcium regulates epidermal growth factor endocytosis in rat pancreas and cultured fibroblasts. Proc. Natl. Acad. Sci. (U. S. A.) 1984; 81: 461–465
   Google Scholar
• Logsdon C. D., Williams J. A. Intracellular Ca2+ and phorbol esters synergistically inhibit internalization of epidermal growth factor in pancreatic acini. Biochem. J. 1984; 223: 893–900
   Google Scholar
• Mössner J., Logsdon C. D., Potau N., Williams J. A., Goldfine I. A. Effect of intracellular Ca2+ on insulin-like growth factor II internalization into pancreatic acini. J. Biol. Chem. 1984; 259: 12350–12356
   Google Scholar
• Gardner J. D., Walker M. D., Rottman A. J. Effect of A 23187 on amylase release from dispersed acini prepared from guinea pig pancreas. Am. J. Physiol. 1980; 238: G458–G466
   Google Scholar
• Merritt J. E., Rubin R. P. Pancreatic amylase secretion and cytoplasmic free calcium. Biochem. J. 1985; 230: 151–159
   PubMed Web of Science ®Google Scholar
• Basu S. K., Goldstein J. L., Anderson R. G. W., Brown M. S. Monensin interrupts the recycling of low density lipoprotein receptors in human fibroblasts. Cell 1981; 24: 493–502
   PubMedGoogle Scholar
• van Leuven F., Cassiman J. J., van den Berghe H. Primary amines inhibit recycling of α2 M receptors in fibroblasts. Cell 1980; 20: 37–43
   PubMedGoogle Scholar
• Kaplan J., Keogh E. A. Analysis of the effect of amines on inhibition of receptor-mediated and fluid-phase pinocytosis in rabbit alveolar macrophages. Cell 1981; 24: 925–932
   Google Scholar
• Whittaker J., Hammond V. A., Garcia-Webb P., Alberti G. The effects of lysosomotropic agents on insulin binding to isolated hepatocytes. Current views on insulin receptors. Serono Symposia, D. Andreani, R. de Pirro, R. Lauro, J. M. Olefsky, J. Roth. Academic Press, London and New York 1981; vol. 41: 219–225
   Google Scholar