Mechanisms mediating caspase activation in cell death

被引:184
作者
Kumar, S
机构
[1] Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Dept Med, Adelaide, SA 5001, Australia
基金
英国医学研究理事会; 英国惠康基金;
关键词
apoptosis; caspases; prodomain; oligomerisation;
D O I
10.1038/sj.cdd.4400600
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
The initial activation of a caspase in a caspase cascade is a crucial event that determines whether a cell will ultimately undergo cell death. Although each cell contains a number of different caspases, only a small subset may be required for apoptosis in response to a specific stimulus. It now seems that each caspase cascade has two types of caspases involved, the upstream or class I caspases, and the downstream or class II caspases. Class I caspases are characterised by long amino-terminal prodomains that carry specific protein-protein interaction domains which mediate oligomerisation of caspases, often assisted by specific adaptor molecules. Oligomerisation appears to be sufficient for autocatalytic activation of class I caspases. Once the first caspase in the pathway has been activated, it processes downstream caspases initiating a cascade of amplifying events that lead to the apoptotic death of a cell. This article reviews our current understanding of mechanisms that mediate the activation of caspases.
引用
收藏
页码:1060 / 1066
页数:7
相关论文
共 79 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   Regulation of apoptotic protease activating factor-1 oligomerization and apoptosis by the WD-40 repeat region [J].
Adrain, C ;
Slee, EA ;
Harte, MT ;
Martin, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (30) :20855-20860
[3]  
Ahmad M, 1997, CANCER RES, V57, P615
[4]   The domains of death: evolution of the apoptosis machinery [J].
Aravind, L ;
Dixit, VM ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (02) :47-53
[5]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[6]   Human CARD4 protein is a novel CED-4/Apaf-1 cell death family member that activates NF-κB [J].
Bertin, J ;
Nir, WJ ;
Fischer, CM ;
Tayber, OV ;
Errada, PR ;
Grant, JR ;
Keilty, JJ ;
Gosselin, ML ;
Robison, KE ;
Wong, GHW ;
Glucksmann, MA ;
DiStefano, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (19) :12955-12958
[7]   Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death [J].
Boldin, MP ;
Goncharov, TM ;
Goltsev, YV ;
Wallach, D .
CELL, 1996, 85 (06) :803-815
[8]   Dimerization and autoprocessing of the Nedd2 (caspase-2) precursor requires both the prodomain and the carboxyl-terminal regions [J].
Butt, AJ ;
Harvey, NL ;
Parasivam, G ;
Kumar, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (12) :6763-6768
[9]   Regulation of cell death protease caspase-9 by phosphorylation [J].
Cardone, MH ;
Roy, N ;
Stennicke, HR ;
Salvesen, GS ;
Franke, TF ;
Stanbridge, E ;
Frisch, S ;
Reed, JC .
SCIENCE, 1998, 282 (5392) :1318-1321
[10]   The death inhibitory molecules CED-9 and CED-4L use a common mechanism to inhibit the CED-3 death protease [J].
Chaudhary, D ;
O'Rourke, K ;
Chinnaiyan, AM ;
Dixit, VM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) :17708-17712