Nitric oxide donors, nitrosothiols and mitochondrial respiration inhibitors induce caspase activation by different mechanisms

被引:62
作者
Borutaite, V
Morkuniene, R
Brown, GC
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] Kaunas Univ Med, Biomed Res Inst, Kaunas, Lithuania
基金
英国生物技术与生命科学研究理事会;
关键词
nitric oxide; apoptosis; macrophage; mitochondrion; caspase;
D O I
10.1016/S0014-5793(00)01140-6
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
We investigated to what extent different types of NO donors induce caspase activation by opening of the mitochondrial permeability transition pore (PTP) or inhibition of mitochondrial respiration. We found that nitrosothiols can directly open the PTP in isolated mitochondria and cause cytochrome c release, whereas NONOate donors can not. In macrophages nitrosothiols cause caspase activation that is blocked by cyclosporin A or calcium chelation, both of which prevent PTP opening, whereas caspase activation caused by NONOates is much less sensitive to these agents. Inhibitors of mitochondrial respiration did not promote PTP opening in isolated mitochondria, and although they cause caspase activation in macrophages, this activation was slower than that caused by NO donors, and was relatively insensitive to cyclosporin and calcium chelators suggesting that PTP opening was not involved. (C) 2000 Federation of European Biochemical Societies.
引用
收藏
页码:155 / 159
页数:5
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