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

被引:92
作者
Wikstrom, Jakob D.
Katzman, Shana M.
Mohamed, Hibo
Twig, Gilad
Graf, Solomon A.
Heart, Emma
Molina, Anthony J. A.
Corkey, Barbara E.
de Vargas, Lina Moitoso
Danial, Nika N.
Collins, Sheila
Shirihai, Orian S.
机构
[1] Tufts Univ, Sch Med, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
[2] Boston Univ, Obes Res Ctr, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Hamner Inst Hlth Sci, Div Translat Biol, Endocrine Biol Program, Res Triangle Pk, NC USA
关键词
D O I
10.2337/db06-0757
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 P-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.
引用
收藏
页码:2569 / 2578
页数:10
相关论文
共 46 条
[1]   Mitochondrial metabolism sets the maximal limit of fuel-stimulated insulin secretion in a model pancreatic beta cell - A survey of four fuel secretagogues [J].
Antinozzi, PA ;
Ishihara, H ;
Newgard, CB ;
Wollheim, CB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (14) :11746-11755
[2]   Glucokinase is an integral component of the insulin granules in glucose-responsive insulin secretory cells and does not translocate during glucose stimulation [J].
Arden, C ;
Harbottle, A ;
Baltrusch, S ;
Tiedge, M ;
Agius, L .
DIABETES, 2004, 53 (09) :2346-2352
[3]   Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production [J].
Arsenijevic, D ;
Onuma, H ;
Pecqueur, C ;
Raimbault, S ;
Manning, BS ;
Miroux, B ;
Couplan, E ;
Alves-Guerra, MC ;
Goubern, M ;
Surwit, R ;
Bouillaud, F ;
Richard, D ;
Collins, S ;
Ricquier, D .
NATURE GENETICS, 2000, 26 (04) :435-439
[4]   Uncoupling proteins 2 and 3 - Potential regulators of mitochondrial energy metabolism [J].
Boss, O ;
Hagen, T ;
Lowell, BB .
DIABETES, 2000, 49 (02) :143-156
[5]   Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3 [J].
Brand, MD ;
Esteves, TC .
CELL METABOLISM, 2005, 2 (02) :85-93
[6]   Uncoupling protein 2 and islet function [J].
Chan, CB ;
Saleh, MC ;
Koshkin, V ;
Wheeler, MB .
DIABETES, 2004, 53 :S136-S142
[7]   Increased uncoupling protein-2 levels in β-cells are associated with impaired glucose-stimulated insulin secretion -: Mechanism of action [J].
Chan, CB ;
De Leo, D ;
Joseph, JW ;
McQuaid, TS ;
Ha, XF ;
Xu, F ;
Tsushima, RG ;
Pennefathner, PS ;
Salapatek, AMF ;
Wheeler, MB .
DIABETES, 2001, 50 (06) :1302-1310
[8]   Overexpression of uncoupling protein 2 inhibits glucose-stimulated insulin secretion from rat islets [J].
Chan, CB ;
MacDonald, PE ;
Saleh, MC ;
Johns, DC ;
Marbàn, E ;
Wheeler, MB .
DIABETES, 1999, 48 (07) :1482-1486
[9]   Emerging functions of mammalian mitochondrial fusion and fission [J].
Chen, HC ;
Chan, DC .
HUMAN MOLECULAR GENETICS, 2005, 14 :R283-R289
[10]   Mitochondria are morphologically and functionally heterogeneous within cells [J].
Collins, TJ ;
Berridge, MJ ;
Lipp, P ;
Bootman, MD .
EMBO JOURNAL, 2002, 21 (07) :1616-1627