Apoptosis induction resulting from proteasome inhibition

被引:201
作者
Shinohara, K
Tomioka, M
Nakano, H
Tone, S
Ito, H
Kawashima, S
机构
[1] TOKYO METROPOLITAN INST MED SCI,DEPT MOL BIOL,BUNKYO KU,TOKYO 113,JAPAN
[2] TOKYO METROPOLITAN INST MED SCI,DEPT RADIAT RES,BUNKYO KU,TOKYO 113,JAPAN
[3] AOYAMA GAKUIN UNIV,FAC SCI & ENGN,DEPT CHEM,SETAGAYA KU,TOKYO 157,JAPAN
关键词
D O I
10.1042/bj3170385
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
Proteases are known to be involved in the apoptotic pathway. We report here that benzyloxycarbonyl(Z)-Leu-Leu-leucinal (ZLLLal), a leupeptin analogue, can induce apoptosis in MOLT-4 and L5178Y cells. ZLLLal is a cell-permeant inhibitor of proteasome. Among the protease inhibitors tested, only calpain inhibitor I (acetyl-Leu-Leu-norleucinal) and ZLLLal caused a marked induction of apoptosis in MOLT-4 cells. In contrast, Z-Leu-leucinal, a specific inhibitor of calpain, did not induce apoptosis. When MOLT-4 cells were incubated in the presence of ZLLLal, p53 accumulated in the cells. These results strongly suggest that inhibition of proteasome induces p53-dependent apoptosis and the proteasome can protect cells from apoptosis.
引用
收藏
页码:385 / 388
页数:4
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