Enhancement of CPP32-like activity in the TNF-treated U937 cells by the proteasome inhibitors

被引:53
作者
Fujita, E
Mukasa, T
Tsukahara, T
Arahata, K
Omura, S
Momoi, T
机构
[1] NCNP,NATL INST NEUROSCI,DIV DEV & DIFFERENTIAT,KODAIRA,TOKYO 187,JAPAN
[2] NCNP,NATL INST NEUROSCI,DEPT NEUROMUSCULAR RES,KODAIRA,TOKYO 187,JAPAN
[3] KITASATO UNIV,KITASATO INST,BIOL FUNCT RES CTR,MINATO KU,TOKYO 108,JAPAN
关键词
D O I
10.1006/bbrc.1996.0986
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
CPP32, which is most closely related To CED-3 in the apoptotic protease in C. elegance, is activated during apoptosis induced by anti-Fas and TNF. Since processing of CPP32 is important for the activation, we examined the effects of protease inhibitors on CPP32-like activity in the TNF-treated U937 cells, Unexpectedly, proteasome inhibitors (at 5 mu M) such as Z-LLnV, Z-LLL, and lactacystin enhanced CPP32-like activity, Ac-DEVD-MCA degrading activity, in the TNF-treated U937 cells in 3 hr, but E64d, cysteine protease inhibitor, did not. These proteasome inhibitors alone did not enhance CPP32-like activity in the untreated U937 cells under the condition used. The proteasome seems to protect the cells from apoptosis by degrading CPP32-like protease or its processing enzyme. (C) 1996 Academic Press, Inc.
引用
收藏
页码:74 / 79
页数:6
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