Bcl-2 protein inhibits oxysterol-induced apoptosis through suppressing CPP32-mediated pathway

被引:50
作者
Harada, K
Ishibashi, S
Miyashita, T
Osuga, J
Yagyu, H
Ohashi, K
Yazaki, Y
Yamada, N
机构
[1] UNIV TOKYO,FAC MED,DEPT INTERNAL MED 3,BUNKYO KU,TOKYO 113,JAPAN
[2] NATL CHILDRENS MED RES CTR,DEPT GENET,TOKYO 154,JAPAN
关键词
oxysterol; apoptosis; cytotoxicity; Bcl-2;
D O I
10.1016/S0014-5793(97)00662-5
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
Oxysterols are presumed to mediate cytotoxicity of oxidized LDL in atherosclerotic lesions. To elucidate its molecular mechanism, we established murine macrophage-like P388-D1 cells which over-express Bcl-2 protein by retrovirus-mediated gene transfer. Oxysterols (7-ketocholesterol, 25-hydroxycholesterol) induced nuclear condensation and oligonucleosomal DNA fragmentation, which were partially inhibited by Bcl-2 over-expression. Though CPP32 inhibitor suppressed the cell death in control cells, it shelved no additive protection in the cells over-expressing Bcl-2. These findings indicate that oxysterols induce apoptosis via Bcl-inhibitable and -uninhibitable pathways, and the former depends on CPP32 activation. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:63 / 66
页数:4
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