Opening of plasma membrane voltage-dependent anion channels (VDAC) precedes caspase activation in neuronal apoptosis induced by toxic stimuli

被引:94
作者
Elinder, F [1 ]
Akanda, N
Tofighi, R
Shimizu, S
Tsujimoto, Y
Orrenius, S
Ceccatelli, S
机构
[1] Linkoping Univ, Dept Biomed & Surg, Div Cell Biol, SE-58185 Linkoping, Sweden
[2] Karolinska Inst, Inst Environm Med, Div Toxicol & Neurotoxicol, SE-17177 Stockholm, Sweden
[3] Osaka Univ, Sch Med, Genet Mol Lab, Suita, Osaka 5650871, Japan
[4] Osaka Univ, Grad Sch Med, Genet Mol Lab, Suita, Osaka 5650871, Japan
关键词
apoptosis; VDAC; patch clamp;
D O I
10.1038/sj.cdd.4401646
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
Apoptotic cell death is an essential process in the development of the central nervous system and in the pathogenesis of its degenerative diseases. Efflux of K+ and Cl- ions leads to the shrinkage of the apoptotic cell and facilitates the activation of caspases. Here, we present electrophysiological and immunocytochemical evidences for the activation of a voltage-dependent anion channel (VDAC) in the plasma membrane of neurons undergoing apoptosis. Anti-VDAC antibodies blocked the channel and inhibited the apoptotic process. In nonapoptotic cells, plasma membrane VDAC1 protein can function as a NADH(-ferricyanide) reductase. Opening of VDAC channels in apoptotic cells was associated with an increase in this activity, which was partly blocked by VDAC antibodies. Hence, it appears that there might be a dual role for this protein in the plasma membrane: (1) maintenance of redox homeostasis in normal cells and (2) promotion of anion efflux in apoptotic cells.
引用
收藏
页码:1134 / 1140
页数:7
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