Support is requested for six projects and three core facilities for a coordinated multi-disciplinary program to investigate the control of exocrine pancreactic function at the cellular and molecular level. The first project on calcium and stimulus secretion coupling in pancreatic acinar cells is concerned with the steps by which acetylcholine acts on muscarinic receptors to mobilize cellular calcium as well as the mechanism by which the rise in cytoplasmic calcium leads to changes in protein phosphorylation and secretion of digestive enzymes. The second project on the regulation of pancreatic cells by insulin and islet hormones is concerned with the physiological regulation of exocrine function by islet hormones including insulin, glucagon, somatostatin and pancreatic polypeptide. It also studies the cellular mechanism of insulin action on acinar cells. The third project on the characterization of receptors for cholecystokinin on acinar cells is concerned with the isolation and characterization of CCK receptors, the long term regulation of CCK receptors and biological responses, and the use of pancreatic acini for a bioassay of CCK in plasma. The fourth project on the regulation of pancreatic growth and differentiation will characterize both the interaction of soluble factors and extracellular matrix components with differentiated acinar and ductal cells, and how the pancreatic cell surface is coupled to the extracellular matrix. The fifth project on hormonal regulation of pancreatic gene expression will analyze the expression of pancreas specific exocrine genes as well as specific membrane antigens. The sixth project on control of pancreatic fluid secretion will use isolated acinar and duct cells as well as reconstituted cellular monolayers to study the mechanism of secretion of pancreatic juice and its regulation by hormones and neurotransmitters. The support requested is for fundamental research, but the resultant knowledge will be relevant to the understanding of pancreatic diseases including cystic fibrosis, pancreatitus and cancer.

Project Start
1984-01-01
Project End
1988-12-31
Budget Start
1985-01-01
Budget End
1985-12-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Szecowka, J; Hallden, G; Goldfine, I D et al. (1989) Purification of the pancreatic cholecystokinin receptor. Regul Pept 24:215-24
Hootman, S R; Ernst, S A (1988) Estimation of Na,K-pump numbers and turnover in intact cells with [3H]ouabain. Methods Enzymol 156:213-29
Okabayashi, Y; Moessner, J; Logsdon, C D et al. (1987) Insulin and other stimulants have nonparallel translational effects on protein synthesis. Diabetes 36:1054-60
Logsdon, C D; Zhang, J C; Guthrie, J et al. (1987) Bombesin binding and biological effects on pancreatic acinar AR42J cells. Biochem Biophys Res Commun 144:463-8
Han, J H; Stratowa, C; Rutter, W J (1987) Isolation of full-length putative rat lysophospholipase cDNA using improved methods for mRNA isolation and cDNA cloning. Biochemistry 26:1617-25
Werlin, S L; Colton, D G; Harb, J et al. (1987) Ontogeny of secretory function and cholecystokinin binding capacity in immature rat pancreas. Life Sci 40:2237-45
Hootman, S R; Brown, M E; Williams, J A (1987) Phorbol esters and A23187 regulate Na+-K+-pump activity in pancreatic acinar cells. Am J Physiol 252:G499-505
Logsdon, C D (1987) Effects of calcium mediated secretagogues on the growth of pancreatic acinar cells in vitro. Gut 28 Suppl:117-20
Lewis, L D; Williams, J A (1987) Structural characterization of the somatostatin receptor in rat anterior pituitary membranes. Endocrinology 121:486-92

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