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beta-Cell mitochondria exhibit membrane potential heterogeneity that can be altered by stimulatory or toxic fuel levels


By JPGRAY - Posted on 24 February 2009

Titlebeta-Cell mitochondria exhibit membrane potential heterogeneity that can be altered by stimulatory or toxic fuel levels
Publication TypeJournal Article
Year of Publication2007
AuthorsWikstrom JD, Katzman SM, Mohamed H, Twig G, Graf SA, Heart E, Molina AJ, Corkey BE, de Vargas LM, Danial NN, Collins S, Shirihai OS
JournalDiabetes
Volume56
Issue10
Pagination2569-78
Date PublishedOct
Publication Languageeng
ISBN Number1939-327X (Electronic)
Accession Number17686943
Key WordsInsulin/*secretion, Glucose/*pharmacology, Cell Culture Techniques, Animals, Microscopy, Confocal, Mice, Knockout, Inbred C57BL, Membrane Potentials/drug effects/*physiology, Male, Ion Channels/deficiency, Insulin-Secreting Cells/cytology/drug effects/*physiology, Calcium/pharmacology, bcl-Associated Death Protein/deficiency, Mitochondrial Proteins/deficiency, Mitochondrial Membranes/drug effects/*physiology/ultrastructure, Magnesium/pharmacology, Islets of Langerhans/cytology/drug effects/physiology
Abstract

OBJECTIVE: beta-Cell response to glucose is characterized by mitochondrial membrane potential (Delta Psi) hyperpolarization and the production of metabolites that serve as insulin secretory signals. We have previously shown that glucose-induced mitochondrial hyperpolarization accompanies the concentration-dependent increase in insulin secretion within a wide range of glucose concentrations. This observation represents the integrated response of a large number of mitochondria within each individual cell. However, it is currently unclear whether all mitochondria within a single beta-cell represent a metabolically homogenous population and whether fuel or other stimuli can recruit or silence sizable subpopulations of mitochondria. This study offers insight into the different metabolic states of beta-cell mitochondria. RESULTS: We show that mitochondria display a wide heterogeneity in Delta Psi and a millivolt range that is considerably larger than the change in millivolts induced by fuel challenge. Increasing glucose concentration recruits mitochondria into higher levels of homogeneity, while an in vitro diabetes model results in increased Delta Psi heterogeneity. Exploration of the mechanism behind heterogeneity revealed that temporary changes in Delta Psi of individual mitochondria, ATP-hydrolyzing mitochondria, and uncoupling protein 2 are not significant contributors to Delta Psi heterogeneity. We identified BAD, a proapoptotic BCL-2 family member previously implicated in mitochondrial recruitment of glucokinase, as a significant factor influencing the level of heterogeneity. CONCLUSIONS: We suggest that mitochondrial Delta Psi heterogeneity in beta-cells reflects a metabolic reservoir recruited by an increased level of fuels and therefore may serve as a therapeutic target.

Notes

1R01DK074778/DK/NIDDK NIH HHS/United States1R21DK070303/DK/NIDDK NIH HHS/United States22RO1DK35914/DK/NIDDK NIH HHS/United States5R01HL071629/HL/NHLBI NIH HHS/United StatesP30 NS047243/NS/NINDS NIH HHS/United StatesP41 RR001395/RR/NCRR NIH HHS/United StatesJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, U.S. Gov't, Non-P.H.S.United States

URLhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17686943
Citation Key534
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