Reversible glutathionylation of complex I increases mitochondrial superoxide formation.

TitleReversible glutathionylation of complex I increases mitochondrial superoxide formation.
Publication TypeJournal Article
Year of Publication2003
AuthorsTaylor, ER, Hurrell, F, Shannon, RJ, Lin, T-K, Hirst, J, Murphy, MP
JournalJ Biol Chem
Volume278
Issue22
Pagination19603-10
Date Published2003 May 30
ISSN0021-9258
KeywordsAnimals, Disulfides, Glutathione, Hydrogen Peroxide, Mitochondria, Liver, NADH Dehydrogenase, Oxidative Stress, Rats, Superoxides
Abstract

Increased production of reactive oxygen species (ROS) by mitochondria is involved in oxidative damage to the organelle and in committing cells to apoptosis or senescence, but the mechanisms of this increase are unknown. Here we show that ROS production by mitochondrial complex I increases in response to oxidation of the mitochondrial glutathione pool. This correlates with thiols on the 51- and 75-kDa subunits of complex I forming mixed disulfides with glutathione. Glutathionylation of complex I increases superoxide production by the complex, and when the mixed disulfides are reduced, superoxide production returns to basal levels. Within intact mitochondria oxidation of the glutathione pool to glutathione disulfide also leads to glutathionylation of complex I, which correlates with increased superoxide formation. In this case, most of this superoxide is converted to hydrogen peroxide, which can then diffuse into the cytoplasm. This mechanism of reversible mitochondrial ROS production suggests how mitochondria might regulate redox signaling and shows how oxidation of the mitochondrial glutathione pool could contribute to the pathological changes that occur to mitochondria during oxidative stress.

DOI10.1074/jbc.M209359200
Alternate JournalJ. Biol. Chem.
Citation Key10.1074/jbc.M209359200
PubMed ID12649289