Superoxide activates mitochondrial uncoupling proteins

被引:1130
作者
Echtay, KS
Roussel, D
St-Pierre, J
Jekabsons, MB
Cadenas, S
Stuart, JA
Harper, JA
Roebuck, SJ
Morrison, A
Pickering, S
Clapham, JC
Brand, MD
机构
[1] MRC, Dunn Human Nutr Unit, Cambridge CB2 2XY, England
[2] GlaxoSmithKline, Dept Comparat Genome, Harlow CM19 5AW, Essex, England
[3] GlaxoSmithKline, Dept Vasc Biol, Harlow CM19 5AW, Essex, England
关键词
D O I
10.1038/415096a
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Uncoupling protein 1 (UCP1) diverts energy from ATP synthesis to thermogenesis in the mitochondria of brown adipose tissue by catalysing a regulated leak of protons across the inner membrane(1,2). The functions of its homologues, UCP2 and UCP3, in other tissues are debated(3,4). UCP2 and UCP3 are present at much lower abundance than UCP1, and the uncoupling with which they are associated is not significantly thermogenic(5,6). Mild uncoupling would, however, decrease the mitochondrial production of reactive oxygen species, which are important mediators of oxidative damage(7,8). Here we show that superoxide increases mitochondrial proton conductance through effects on UCP1, UCP2 and UCP3. Superoxide-induced uncoupling requires fatty acids and is inhibited by purine nucleotides. It correlates with the tissue expression of UCPs, appears in mitochondria from yeast expressing UCP1, and is absent in skeletal muscle mitochondria from UCP3 knockout mice. Our findings indicate that the interaction of superoxide with UCPs may be a mechanism for decreasing the concentrations of reactive oxygen species inside mitochondria.
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页码:96 / 99
页数:4
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