The intracellular redox state is a core determinant of mitochondrial fusion

EMBO Rep. 2012 Oct;13(10):909-15. doi: 10.1038/embor.2012.128. Epub 2012 Sep 4.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytosol / enzymology
  • Cytosol / metabolism
  • GTP Phosphohydrolases / metabolism
  • Glutathione Disulfide / metabolism*
  • Guanosine Triphosphate / metabolism
  • HeLa Cells
  • Humans
  • Hydrolysis
  • Mitochondrial Dynamics*
  • Mitochondrial Proteins / metabolism
  • Oxidation-Reduction
  • Oxidative Stress*

Substances

  • Mitochondrial Proteins
  • Guanosine Triphosphate
  • GTP Phosphohydrolases
  • MFN2 protein, human
  • Glutathione Disulfide