Induction of apoptosis by valinomycin: mitochondrial permeability transition causes intracellular acidification

被引:70
作者
Furlong, IJ
Mediavilla, CL
Ascaso, R
Rivas, AL
Collins, MKL
机构
[1] Inst Canc Res, Chester Beatty Labs, CRC, Ctr Cell & Mol Biol, London SW3 6JB, England
[2] CSIC, Inst Parasitol & Biomed, Granada 18001, Spain
关键词
apoptosis; valinomycin; intracellular pH; mitochondrial permeability transition;
D O I
10.1038/sj.cdd.4400335
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
In order to determine whether disruption of mitochondrial function could trigger apoptosis in murine haematopoietic cells, we used the potassium ionophore valinomycin. Valinomycin induces apoptosis in the murine pre-B cell line BAF3, which cannot be inhibited by interleukin-3 addition or Bcl-2 over-expression. Valinomycin triggers rapid loss of mitochondrial membrane potential. This precedes cytoplasmic acidification, which leads to cysteine-active-site protease activation, DNA fragmentation and cell death. Bongkrekic acid, an inhibitor of the mitochondrial permeability transition, prevents acidification and subsequent induction of apoptosis by valinomycin.
引用
收藏
页码:214 / 221
页数:8
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