Bcl-xS induces an NGF-inhibitable cytochrome c release

被引:11
|
作者
Lindenboim, L
Schlipf, S
Kaufmann, T
Borner, C
Stein, R [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Neurobiochem, IL-69978 Tel Aviv, Israel
[2] Univ Freiburg, Inst Mol Med & Cell Res, ZFK, D-79106 Freiburg, Germany
关键词
apoptosis; Bcl-2; cytochrome c; NGF; Bcl-x(S);
D O I
10.1016/j.yexcr.2004.03.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bcl-xs, a pro-apoptotic member of the Bcl-2 protein family, is localized in the mitochondrial outer membrane and induces caspase-dependent and nerve growth factor (NGF)-inhibitable apoptosis in PC12 cells. The mechanism of action of Bcl-x(S) and how NGF inhibits this death are not fully understood. It is still unknown whether Bcl-x(S) induces mitochondrial cytochrome c release, and which apoptotic step NGF inhibits. We show that Bcl-x(S) induces cytochrome c release and caspase-3 activation in several cell types, and that in PC 12 cells, these events are inhibited by NGF treatment. The survival effect of NGF was inhibited by inhibitors of protein kinase C (PKC), phosphatidylinositol-3-kinase (PI 3-kinase), and the mitogen-activated protein kinase kinase (MEK) inhibitors GF 109203X, LY294002, and U0126. These findings show that cytochrome c release and caspase-3 activation participate in Bcl-x(S)-induced apoptosis, and that NGF inhibits Bcl-x(S)-induced apoptosis at the mitochondrial level via the PKC, PI 3-kinase, and MEK signaling pathways. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:392 / 403
页数:12
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