1. ABSTRACT The islets of Langerhans are ordered assemblies of different endocrine cell types which interact one with the others to maintain an optimal hormonal output. Junctional-mediated exchanges of ions and molecules (ionic and metabolic coupling) between islet cells may play a role in the control of such an integrated activity. To test this hypothesis, a combined morphological and physiological study of coupling and secretion of insulin-producing B-cells is proposed. We plan to characterize the membrane specializations mediating B-cell coupling, by quantitating the development and structure of gap and tight junctions, as revealed by freeze-fracture in isolated rat islets, and to determine how these correlate with secretory events and intercellular exhanges of ions and molecules. The occurrence and regulation of direct molecular exchanges between B-cells as well as between B- and non B-cells, will be studied, under different conditions of insulin secretion, by following the transfer of fluorescent and radioactive molecules, introduced in endocrine islet cells either in culture or within whole islets. Ionic exchanges will be followed by electrophysiology in the same systems. Both morphological and physiological studies will be carried out on islets from control and experimental diabetic rats to assess whether hormonal abnormalities precede or follow perturbations of islet cell coupling. This approach is designed to provide new information on both the control of B-cell secretion and the function of B-cell coupling. Hopefully, this will help to understand the pathogenesis of certain forms of diabetes, which may be attributable to faulty communication among islet cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM030519-04
Application #
3152082
Study Section
Metabolism Study Section (MET)
Project Start
1982-02-01
Project End
1987-01-31
Budget Start
1985-02-01
Budget End
1986-01-31
Support Year
4
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Chanson, M; Bruzzone, R; Bosco, D et al. (1989) Effects of n-alcohols on junctional coupling and amylase secretion of pancreatic acinar cells. J Cell Physiol 139:147-56
Bosco, D; Chanson, M; Bruzzone, R et al. (1988) Visualization of amylase secretion from individual pancreatic acini. Am J Physiol 254:G664-70
Salomon, D; Saurat, J H; Meda, P (1988) Cell-to-cell communication within intact human skin. J Clin Invest 82:248-54
Meda, P; Bruzzone, R; Chanson, M et al. (1987) Gap junctional coupling modulates secretion of exocrine pancreas. Proc Natl Acad Sci U S A 84:4901-4
Light, D B; Van Eenenaam, D P; Sorenson, R L et al. (1987) Potassium-selective ion channels in a transformed insulin-secreting cell line. J Membr Biol 95:63-72
Michaels, R L; Sorenson, R L; Parsons, J A et al. (1987) Prolactin enhances cell-to-cell communication among beta-cells in pancreatic islets. Diabetes 36:1098-103
Bruzzone, R; Trimble, E R; Gjinovci, A et al. (1987) Regulation of pancreatic exocrine function: a role for cell-to-cell communication? Pancreas 2:262-71
Stefan, Y; Meda, P; Neufeld, M et al. (1987) Stimulation of insulin secretion reveals heterogeneity of pancreatic B cells in vivo. J Clin Invest 80:175-83
Knodel, S; Meda, P; Orci, L (1987) Rapid in vitro formation of smooth endoplasmic reticulum aggregates within peptide-producing islet cells. J Cell Physiol 133:111-8
Chertow, B S; Blaner, W S; Baranetsky, N G et al. (1987) Effects of vitamin A deficiency and repletion on rat insulin secretion in vivo and in vitro from isolated islets. J Clin Invest 79:163-9

Showing the most recent 10 out of 14 publications