Caspase activation cascades in apoptosis

被引:160
作者
Logue, Susan E. [1 ]
Martin, Seamus J. [1 ]
机构
[1] Univ Dublin Trinity Coll, Dept Genet, Smurfit Inst, Mol Cell Biol Lab, Dublin 2, Ireland
基金
英国惠康基金;
关键词
D O I
10.1042/BST0360001
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
Apoptosis, a highly controlled mode of cell death, is utilized to eliminate superfluous, aged, injured or infected cells from the body. Caspases, a family of aspartic acid-specific proteases, are the major effectors of apoptosis. To curtail their activity, caspases are normally synthesized as inactive precursors, but become activated at the onset of apoptosis by activation signals. Once active, caspases preside over the ordered dismantling of the cell through restricted proteolysis of hundreds of substrate proteins. Over the last 10 years, intense research has focused upon the pathways that control caspase activation. Although some, such as the apoptosome and death receptor-mediated pathways to caspase activation, are well established, others are less clearly defined. In this review, we discuss current perspectives concerning the diverse pathways to caspase activation.
引用
收藏
页码:1 / 9
页数:9
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