Essential role for caspase-8 in transcription-independent apoptosis triggered by p53

被引:120
作者
Ding, HF
Lin, YL
McGill, G
Juo, P
Zhu, H
Blenis, J
Yuan, JY
Fisher, DE
机构
[1] Dana Farber Canc Inst, Div Pediat Hematol Oncol, Dept Pediat Hematol Oncol, Boston, MA 02115 USA
[2] Childrens Hosp, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1074/jbc.M004714200
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
p53's dual regulation of arrest versus apoptosis may underlie tumor-selective effects of anti-cancer therapy. p53's apoptotic effect has been suggested to involve both transcription-dependent and -independent mechanisms. It is shown here that caspase-8 is activated early in cells undergoing p53-mediated apoptosis and in S100 cell-free extracts that recapitulate transcription-independent apoptosis, Depletion or inactivation of caspase-8 either in cells or cell-free extracts completely prevents this transcription-independent apoptosis and significantly attenuates overall death induced by wildtype p53. Importantly, caspase-8 activation appears to be independent of FADD, and caspase-8 is found in a novel 600-kDa complex following p53 activation. These findings highlight the roles of both transcription-dependent and -independent apoptosis by p53 and identify an essential role for caspase-8 in the transcription-independent pathway.
引用
收藏
页码:38905 / 38911
页数:7
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