Activation of caspase-3-like protease by digitonin-treated lysosomes

被引:105
作者
Ishisaka, R
Utsumi, T
Yabuki, M
Kanno, T
Furuno, T
Inoue, N
Utsumi, K
机构
[1] Kurashiki Med Ctr, Inst Med Sci, Kurashiki, Okayama 7108522, Japan
[2] Yamaguchi Univ, Fac Agr, Dept Biol Chem, Yamaguchi 7538515, Japan
[3] Kochi Med Sch, Dept Med & Gerontol, Nankoku, Kochi 7838505, Japan
[4] Osaka City Univ, Sch Med, Dept Biochem, Abeno Ku, Osaka 5458585, Japan
来源
FEBS LETTERS | 1998年 / 435卷 / 2-3期
关键词
apoptosis; digitonin treatment; caspase-3; cathepsin; lysosomal protease; protease inhibitor;
D O I
10.1016/S0014-5793(98)01080-1
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
Apoptosis, a naturally occurring programmed cell death or cell 'suicide', has been paid much attention as one of the critical mechanisms for morphogenesis and tissue remodeling. Activation of cysteine aspartases (caspases) is one of the critical steps leading to apoptosis, Although a mitochondria-mediated pathway has been postulated to be one of the activation mechanism of caspase-3, another subcellular compartment might be involved in the activation of the enzyme. The present study shows that the supernatant fraction of digitonin-treated lysosomes strongly activates Ac-DEVD-CHO inhibitable caspase-3-like protease, Activation of caspase-3-like protease by digitonin-treated lysosomal fractions was specifically suppressed hy leupeptin and E-64, inhibitors of cysteine protease, These results indicate that leakage of lysosomal cysteine protease(s) into the cytosolic compartment might be involved in the activation of caspase-3-like protease, (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:233 / 236
页数:4
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