共 28 条
Comparison of the anti-apoptotic effects of Bcr-Abl, Bcl-2 and Bcl-XL following diverse apoptogenic stimuli
被引:36
作者:

Brumatti, G
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机构: Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil

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机构:

Chehab, CF
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil

Yon, M
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h-index: 0
机构: Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil

Amarante-Mendes, GP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil
机构:
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil
[2] Millenium Inst, Inst Invest Immunol, BR-05508900 Sao Paulo, Brazil
基金:
巴西圣保罗研究基金会;
关键词:
apoptosis;
Bcr-Abl;
Bcl-2;
Bcl-X-L;
mitochondrion;
D O I:
10.1016/S0014-5793(03)00299-0
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:
Ectopic expression of Bcr-Abl, Bcl-2 or Bcl-x(L) in HL-60 cells conferred resistance to apoptosis against a variety of death-inducing agents. Bcr-Abl-mediated interference with mitochondrial events was confirmed by the analysis of the loss of mitochondrial transmembrane potential and cytochrome c release. RL-60.Bcr-Abl cells were extremely resistant to all apoptogenic stimuli tested, even in circumstances where HL-60.Bcl-2 or HL-60.Bcl-x(L) cells were only partially protected from apoptosis. The levels of Mcl-1, Bax, Bid, Akt, c-IAP-1, c-IAP-2, XIAP and c-FLIP were compared in all HL-60 lines. Our findings show that Bcr-Abl is a more powerful anti-apoptotic molecule than Bcl-2 or Bcl-x(L). (C) 2003 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
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页码:57 / 63
页数:7
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