The intracellular redox state is a core determinant of mitochondrial fusion

被引:209
|
作者
Shutt, Timothy [2 ]
Geoffrion, Michele [2 ]
Milne, Ross [2 ]
McBride, Heidi M. [1 ]
机构
[1] Montreal Neurol Hosp & Inst, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[2] Univ Ottawa, Inst Heart, Ottawa, ON K1Y 4W7, Canada
关键词
mitochondria; fusion; glutathione; stress; mitofusin; S-GLUTATHIONYLATION; MEMBRANE-FUSION; COMPLEXES; CELL; DEGRADATION; SWITCH;
D O I
10.1038/embor.2012.128
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial hyperfusion has recently been shown to function as a cellular stress response, providing transient protection against apoptosis and mitophagy. However, the mechanisms that mediate this response remain poorly understood. In this study, we demonstrate that oxidized glutathione (GSSG), the core cellular stress indicator, strongly induces mitochondrial fusion. Biochemical and functional experiments show that GSSG induces the generation of disulphide-mediated mitofusin oligomers, in a process that also requires GTP hydrolysis. Our data outline the molecular events that prime the fusion machinery, providing new insights into the coupling of mitochondrial fusion with the cellular stress response.
引用
收藏
页码:909 / 915
页数:7
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