Bioartificial pancreata promise physiological control of blood glucose levels, effectively treating Type I diabetes mellitus. Given the short supply of islets, development of alternative cell-lines appropriate for use in such devices is necessary. Transformed cells are a viable option, though their bioenergetic machinery may be inefficient. Because bioenergetics plays a role in the secretion of insulin, determining bioenergetic factors critical to insulin secretion may be important in selecting appropriate lines for inclusion into a bioartificial pancreas. This proposal will study cultures of entrapped transformed insulinoma cells and determine the impact of ATP and anaplerotic pathways on their ability to secrete insulin in response to an external glucose stimulus. NMR spectroscopic analysis of 13C and 31P data will provide a non-invasive quantitative assessment of the coupling between energy metabolism and insulin secretion, while non-NMR assays will derive glucose and oxygen consumption rates, as well as lactate, NH4+ and insulin production rates to provide a metabolic profile. Administration of specific inhibitors of the TCA cycle, anaplerotic pathways and oxidative phosphorylation, will aid in identifying factors critical to the initiation of insulin secretion. This knowledge will aid in the rational design and selection of insulin-producing cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DK009941-02
Application #
6214005
Study Section
Special Emphasis Panel (ZRG1-SB (01))
Program Officer
Hyde, James F
Project Start
2000-03-01
Project End
Budget Start
2000-03-01
Budget End
2001-02-28
Support Year
2
Fiscal Year
2000
Total Cost
$37,516
Indirect Cost
Name
Emory University
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Simpson, N E; Bennett, L K; Papas, K K et al. (2000) Effects of pH on murine insulinoma betaTC3 cells. Biochem Biophys Res Commun 273:937-41