Caspase-2 redux

被引:114
作者
Troy, CM
Shelanski, ML
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pathol, Taub Inst Study Alzheimers Dis & Aging Brain, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
caspase; caspase-2; RAIDD; caspase inhibition; caspase activation; caspase activity; antisense oligonucleotides; siRNA;
D O I
10.1038/sj.cdd.4401175
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
It has been difficult to assign caspase-2 to the effector or initiator caspase groups. It bears sequence homology to initiators (caspase-9 and CED-3), but its cleavage specificity is closer to the effectors (caspase-3 and -7). Interest in caspase-2 was dampened by the lack of a dramatic phenotype in the caspase-2 null mouse. Studies have been inhibited by the lack of knowledge about its mechanism of activation and the lack of specific methods to assay its activity. Molecular studies have defined a unique role for caspase-2 in apoptosis initiated by beta-amyloid toxicity or by trophic factor deprivation. Recently, a role for caspase-2 as an upstream initiator of mitochondrial permeabilization has been proposed. Thus, while much remains to be deciphered about caspase-2, most critically the mode of activation, it is clear that caspase-2 plays critical and singular roles in the control of programmed cell death.
引用
收藏
页码:101 / 107
页数:7
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