A novel, high conductance channel of mitochondria linked to apoptosis in mammalian cells and Bax expression in yeast

被引:229
作者
Pavlov, EV
Priault, M
Pietkiewicz, D
Cheng, EHY
Antonsson, B
Manon, S
Korsmeyer, SJ
Mannella, CA
Kinnally, KW
机构
[1] NYU, Coll Dent, Div Basic Sci, New York, NY 10010 USA
[2] CNRS, Inst Biochim & Genet Cellulaires, F-33077 Bordeaux, France
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Howard Hughes Med Inst,Dept Pathol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Howard Hughes Med Inst,Dept Med, Boston, MA 02115 USA
[5] Serono Int SA, Serono Pharmaceut Res Inst, CH-1228 Plan Les Ouates, Switzerland
[6] New York State Dept Hlth, Wadsworth Ctr, Albany, NY 12203 USA
关键词
D O I
10.1083/jcb.200107057
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During apoptosis, proapoptotic factors are released from mitochondria by as yet undefined mechanisms. Patch-clamping of mitochondria and proteoliposomes formed from mitochondrial outer membranes of mammalian (FL5.12) cells has uncovered a novel ion channel whose activity correlates with onset of apoptosis. The pore diameter inferred from the largest conductance state of this channel is similar to4 nm, sufficient to allow diffusion of cytochrome c and even larger proteins. The activity of the channel is affected by Bcl-2 family proteins in a manner consistent with their pro- or antiapoptotic properties. Thus, the channel activity correlates with presence of proapoptotic Bax in the mitochondrial outer membrane and is absent in mitochondria from cells overexpressing antiapoptotic Bcl-2. Also, a similar channel activity is found in mitochondrial outer membranes of yeast expressing human Bax. These findings implicate this channel, named mitochondrial apoptosis-induced channel, as a candidate for the outer-membrane pore through which cytochrome c and possibly other factors exit mitochondria during apoptosis.
引用
收藏
页码:725 / 731
页数:7
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