Contrasting effects of NO and peroxynitrites on HSP70 expression and apoptosis in human monocytes

被引:34
作者
Adrie, C
Richter, C
Bachelet, M
Banzet, N
François, D
Dinh-Xuan, AT
Dhainaut, JF
Polla, BS
Richard, MJ
机构
[1] Univ Paris 05, Unite Format & Rech Cochin Port Royal, Physiol Resp Lab, Paris, France
[2] Cochin Port Royal Hosp, Med Intens Care Unit, Paris, France
[3] Swiss Fed Inst Technol, Inst Biochem, Zurich, Switzerland
[4] A Michallon Hosp, Lab Biol Oxidat Stress, Grenoble, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2000年 / 279卷 / 02期
关键词
nitric oxide; heat shock; cell stress; cell death;
D O I
10.1152/ajpcell.2000.279.2.C452
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The free radicals nitric oxide (. NO) and superoxide (O-2(-).) react to form peroxynitrite (ONOO-), a highly toxic oxidant species. In this study we investigated the respective effects of NO and ONOO- in monocytes from healthy human donors. Purified monocytes were incubated for 6 or 16 h with a pure NO donor (S-nitroso-N-acetyl-DL-penicillamine, 0-2 mM), an . NO/ONOO- donor (3-morpholinosydnonimine chlorhydrate, 0-2 mM) with and without superoxide dismutase (200 IU/ml), or pure ONOO-. We provide evidence that 3-morpholinosydnonimine chlorhydrate alone represents a strong stress to human monocytes leading to a dose-dependent increase in heat shock protein-70 (HSP70) expression, mitochondrial membrane depolarization, and cell death by apoptosis and necrosis. These phenomena were abolished by superoxide dismutase, suggesting that ONOO-, but not . NO, was responsible for the observed effects. This observation was further strengthened by the absence of a stress response in cells exposed to S-nitroso-N-acetyl-DL-penicillamine. Conversely, exposure of cells to ONOO- alone also induced mitochondrial membrane depolarization and cell death by apoptosis and necrosis. Thus ONOO- formation may well explain the toxic effect generally attributed to . NO.
引用
收藏
页码:C452 / C460
页数:9
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