Mitochondrial factors with dual roles in death and survival

被引:57
作者
Cheng, W. -C
Berman, S. B.
Ivanovska, I.
Jonas, E. A.
Lee, S. J.
Chen, Y.
Kaczmarek, L. K.
Pineda, F.
Hardwick, J. M.
机构
[1] Johns Hopkins Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] Johns Hopkins Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[3] Johns Hopkins Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[4] Johns Hopkins Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[5] Yale Univ, Dept Endocrinol, New Haven, CT 06520 USA
[6] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[7] Univ Pittsburgh, Dept Pharmacol, Pittsburgh, PA 15260 USA
关键词
apoptosis; Fis1; CED-9; yeast; aging; virus;
D O I
10.1038/sj.onc.1209596
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
At least in mammals, we have some understanding of how caspases facilitate mitochondria-mediated cell death, but the biochemical mechanisms by which other factors promote or inhibit programmed cell death are not understood. Moreover, most of these factors are only studied after treating cells with a death stimulus. A growing body of new evidence suggests that cell death regulators also have 'day jobs' in healthy cells. Even caspases, mitochondrial fission proteins and pro-death Bcl-2 family proteins appear to have normal cellular functions that promote cell survival. Here, we review some of the supporting evidence and stretch beyond the evidence to seek an understanding of the remaining questions.
引用
收藏
页码:4697 / 4705
页数:9
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