The most unkindest cut of all*: on the multiple roles of mammalian caspases

被引:89
作者
Fadeel, B [1 ]
Orrenius, S [1 ]
Zhivotovsky, B [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Toxicol, S-17177 Stockholm, Sweden
关键词
apoptosis; caspase; chemotherapy; Fas; inflammation; leukemia;
D O I
10.1038/sj.leu.2401871
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The caspases, first discovered almost a decade ago, are intracellular cysteine proteases which have been shown to play an esssential role in the initiation and execution phases of apoptotic cell death. Numerous strategies for the activation and inhibition of these 'killer' proteases have evolved, including the regulation of caspase expression and function at the transcriptional and post-translational level, as well as the expression of viral and cellular inhibitors of caspases. Emerging evidence in recent years has also implicated the caspases in various, non-apoptotic aspects of cellular physiology, such as cytokine processing during inflammation, differentiation of progenitor cells during erythropoiesis and lens fiber development, and proliferation of T lymphocytes, thus attesting to the pleiotropic functions of these proteases. The present review aims to discuss the multiple roles of the mammalian caspases with particular emphasis on their activation and regulation in cells of leukemic origin and the attendant possibilities of therapeutic intervention.
引用
收藏
页码:1514 / 1525
页数:12
相关论文
共 169 条
[101]   Caspase structure, proteolytic substrates, and function during apoptotic cell death [J].
Nicholson, DW .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (11) :1028-1042
[102]  
Nomura M, 1999, CANCER RES, V59, P5542
[103]   2-Chloro-2′-deoxyadenosine induces apoptosis through the Fas/Fas ligand pathway in human leukemia cell line MOLT-4 [J].
Nomura, Y ;
Inanami, O ;
Takahashi, K ;
Matsuda, A ;
Kuwabara, M .
LEUKEMIA, 2000, 14 (02) :299-306
[104]   Cleavage of the calpain inhibitor, calpastatin, during apoptosis [J].
Pörn-Ares, MI ;
Samali, A ;
Orrenius, S .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (12) :1028-1033
[105]  
REED JC, 2000, SCIENCE, V287, pA1363
[106]  
RODRIGUEZ J, 2000, SCIENCE, V287, pA1363, DOI DOI 10.1126/SCIENCE.287.5457.1363A
[107]   Bcl-2 prolongs cell survival after Bax-induced release of cytochrome c [J].
Rossé, T ;
Olivier, R ;
Monney, L ;
Rager, M ;
Conus, S ;
Fellay, I ;
Jansen, B ;
Borner, C .
NATURE, 1998, 391 (6666) :496-499
[108]   Membrane and morphological changes in apoptotic cells regulated by caspase-mediated activation of PAK2 [J].
Rudel, T ;
Bokoch, GM .
SCIENCE, 1997, 276 (5318) :1571-1574
[109]   Implication of calpain in caspase activation during B cell clonal deletion [J].
Ruiz-Vela, A ;
de Buitrago, GG ;
Martínez-A, C .
EMBO JOURNAL, 1999, 18 (18) :4988-4998
[110]   Acinus is a caspase-3-activated protein required for apoptotic chromatin condensation [J].
Sahara, S ;
Aoto, M ;
Eguchi, Y ;
Imamoto, N ;
Yoneda, Y ;
Tsujimoto, Y .
NATURE, 1999, 401 (6749) :168-173