The first specific aim of the previously funded research proposal was to characterize secretory granules within living primary-cultured, pancreatic beta cells at rest and upon stimulation. A primary reason for this renewal application is the considerable effort and time required to establish a reliable method for preparing primary-cultured beta cells. With that method established, an additional year of support should be sufficient time to complete the work outlined below. The work included in this request for continued funding will expand upon a very intriguing observation made during the first period of support. That is, upon stimulation with both potassium and glucose, fluorescent-labeled secretory vesicles in primary-cultured pancreatic beta cells brighten substantially while apparently remaining inside of the cell. This observation is quite unlike the response seen in chromaffin cells where stimulation leads to the rapid disappearance of the fluorescently labeled vesicles. These results suggest a fundamental difference in the secretion mechanisms of two closely related cell types. Additionally, in response to glucose steps, the pattern of these vesicle brightening appears pulsatile. With TIRF microscopy, it is possible to quantify pulse mass and frequency at the single granule level. The results of the studies outlined in this proposal will provide key insight into insulin secretion at the single cell level.

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 #
2F32DK010181-03
Application #
6649020
Study Section
Special Emphasis Panel (ZRG1-F06 (20))
Program Officer
Hyde, James F
Project Start
2003-02-01
Project End
2004-01-31
Budget Start
2003-02-01
Budget End
2004-01-31
Support Year
3
Fiscal Year
2003
Total Cost
$46,420
Indirect Cost
Name
University of Southern California
Department
Physiology
Type
Schools of Medicine
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Michael, Darren J; Tapechum, Sompol; Rohan, Joyce G et al. (2009) Fluorescent cargo proteins in peptidergic endocrine cells: cell type determines secretion kinetics at exocytosis. Ann N Y Acad Sci 1152:7-17
Michael, Darren J; Xiong, Wenyong; Geng, Xuehui et al. (2007) Human insulin vesicle dynamics during pulsatile secretion. Diabetes 56:1277-88
Michael, Darren J; Ritzel, Robert A; Haataja, Leena et al. (2006) Pancreatic beta-cells secrete insulin in fast- and slow-release forms. Diabetes 55:600-7
Michael, Darren J; Cai, Haijiang; Xiong, Wenyong et al. (2006) Mechanisms of peptide hormone secretion. Trends Endocrinol Metab 17:408-15
Michael, Darren J; Geng, Xuehui; Cawley, Niamh X et al. (2004) Fluorescent cargo proteins in pancreatic beta-cells: design determines secretion kinetics at exocytosis. Biophys J 87:L03-5