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蛋白酶体抑制导致的细胞凋亡诱导

Apoptosis induction resulting from proteasome inhibition.

作者信息

Shinohara K, Tomioka M, Nakano H, Toné S, Ito H, Kawashima S

机构信息

Department of Radiation Research, Tokyo Metropolitan Institute of Medical Science, Japan.

出版信息

Biochem J. 1996 Jul 15;317 ( Pt 2)(Pt 2):385-8. doi: 10.1042/bj3170385.

Abstract

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 that proteasome can protect cell from apoptosis.

摘要

已知蛋白酶参与凋亡途径。我们在此报告,亮抑酶肽类似物苄氧羰基(Z)-亮氨酸-亮氨酸-亮氨醛(ZLLLal)可诱导MOLT-4和L5178Y细胞凋亡。ZLLLal是一种可穿透细胞的蛋白酶体抑制剂。在测试的蛋白酶抑制剂中,只有钙蛋白酶抑制剂I(乙酰基-亮氨酸-亮氨酸-正亮氨醛)和ZLLLal能在MOLT-4细胞中显著诱导凋亡。相比之下,钙蛋白酶的特异性抑制剂Z-亮氨醛则不会诱导凋亡。当MOLT-4细胞在ZLLLal存在的情况下孵育时,细胞内会积累p53。这些结果有力地表明,蛋白酶体的抑制会诱导p53依赖性凋亡,并且蛋白酶体可以保护细胞免于凋亡。

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