Multiple species of CPP32 and Mch2 are the major active caspases present in apoptotic cells

被引:322
作者
Faleiro, L [1 ]
Kobayashi, R [1 ]
Fearnhead, H [1 ]
Lazebnik, Y [1 ]
机构
[1] SUNY STONY BROOK,GRAD PROGRAM MOL & CELLULAR BIOL,STONY BROOK,NY 11794
关键词
affinity labels; apoptosis; cancer therapy; caspases (ICE-like proteases); proteases;
D O I
10.1093/emboj/16.9.2271
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 activity of ICE-like proteases or caspases is essential for apoptosis. Multiple caspases participate in apoptosis in mammalian cells but how many caspases are involved and what is their relative contribution to cell death is poorly understood, To identify caspases activated in apoptotic cells, we developed an approach to simultaneously detect multiple active caspases. Using tumor cells as a model, we have found that CPP32 (caspase 3) and Mch2 (caspase 6) are the major active caspases in apoptotic cells, and are activated in response to distinct apoptosis-inducing stimuli and in all cell lines analyzed. Both CPP32 and Mch2 are present in apoptotic cells as multiple active species. In a given cell line these species remained the same irrespective of the apoptotic stimulus used, However, the species of CPP32 and Mch2 detected varied between cell lines, indicating differences in caspase processing. The strategy described here is widely applicable to identify active caspases involved in apoptosis.
引用
收藏
页码:2271 / 2281
页数:11
相关论文
共 36 条
[1]   Human ICE/CED-3 protease nomenclature [J].
Alnemri, ES ;
Livingston, DJ ;
Nicholson, DW ;
Salvesen, G ;
Thornberry, NA ;
Wong, WW ;
Yuan, JY .
CELL, 1996, 87 (02) :171-171
[2]   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
[3]  
Chinnaiyan AM, 1996, CURR BIOL, V6, P555
[4]   Sequential activation of ICE-like and CPP32-like proteases during Fas-mediated apoptosis [J].
Enari, M ;
Talanian, RV ;
Wong, WW ;
Nagata, S .
NATURE, 1996, 380 (6576) :723-726
[5]   Identification of a cysteine protease closely related to interleukin-1 beta-converting enzyme [J].
Faucheu, C ;
Blanchet, AM ;
CollardDutilleul, V ;
Lalanne, JL ;
DiuHercend, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 236 (01) :207-213
[6]  
FERNANDESALNEMRI T, 1995, CANCER RES, V55, P6045
[7]  
FERNANDESALNEMRI T, 1995, CANCER RES, V55, P2737
[8]  
FERNANDESALNEMRI T, 1994, J BIOL CHEM, V269, P30761
[9]   A license to kill [J].
Fraser, A ;
Evan, G .
CELL, 1996, 85 (06) :781-784
[10]   The serine protease inhibitors, tosylphenylalanine chloromethyl ketone and tosyllysine chloromethyl ketone, potently inhibit pp70(s6k) activation [J].
Grammer, TC ;
Blenis, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (39) :23650-23652