The induction of GSH synthesis by nanomolar concentrations of NO in endothelial cells:: a role for γ-glutamylcysteine synthetase and γ-glutamyl transpeptidase

被引:111
作者
Moellering, D
Mc Andrew, J
Patel, RP
Forman, HJ
Mulcahy, RT
Jo, H
Darley-Usmar, VM
机构
[1] Univ Alabama, Dept Pathol, Mol & Cellular Div, Birmingham, AL 35294 USA
[2] Univ Alabama, Ctr Free Rad Biol, Birmingham, AL 35294 USA
[3] Univ So Calif, Los Angeles, CA 90033 USA
[4] Univ Wisconsin, Dept Human Oncol, Madison, WI 53792 USA
关键词
glutathione; endothelial cell; nitric oxide; gamma-glutamylcysteine synthetase; atherosclerosis; gamma-glutamyl transpeptidase;
D O I
10.1016/S0014-5793(99)00371-3
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
Nitric oxide protects cells from oxidative stress through a number of direct scavenging reactions with free radicals but the effects of nitric oxide on the regulation of antioxidant enzymes are only now emerging. Using bovine aortic endothelial cells as a model, we show that nitric oxide, at physiological rates of production (1-3 nM/s), is capable of inducing the synthesis of glutathione through a mechanism involving gamma-glutamylcysteine synthetase and gamma-glutamyl transpeptidase. This novel nitric oxide signalling pathway is cGMP independent and we hypothesize that it makes an important contribution to the anti-atherosclerotic and antioxidant properties of nitric oxide. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:292 / 296
页数:5
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