Two distinct signaling pathways regulate peroxynitrite-induced apoptosis in PC12 cells

被引:0
|
作者
J J Shacka
M A Garner
J D Gonzalez
Y-Z Ye
T L D'Alessandro
A G Estévez
机构
[1] University of Alabama at Birmingham,Department of Physiology and Biophysics
[2] Burke/Cornell Medical Research Institute,Department of Pharmacology and Toxicology
[3] University of Alabama at Birmingham,Department of Neurobiology
[4] University of Alabama at Birmingham,Division of Neuropathology, Department of Pathology
[5] Center for Free Radical Biology,undefined
[6] University of Alabama at Birmingham,undefined
[7] University of Alabama at Birmingham,undefined
[8] Burke/Cornell Medical Research Institute,undefined
来源
Cell Death & Differentiation | 2006年 / 13卷
关键词
peroxynitrite; apoptosis; mitochondria; MAPK; Akt;
D O I
暂无
中图分类号
学科分类号
摘要
The mechanisms of peroxynitrite-induced apoptosis are not fully understood. We report here that peroxynitrite-induced apoptosis of PC12 cells requires the simultaneous activation of p38 and JNK MAP kinase, which in turn activates the intrinsic apoptotic pathway, as evidenced by Bax translocation to the mitochondria, cytochrome c release to the cytoplasm and activation of caspases, leading to cell death. Peroxynitrite induces inactivation of the Akt pathway. Furthermore, overexpression of constitutively active Akt inhibits both peroxynitrite-induced Bax translocation and cell death. Peroxynitrite-induced death was prevented by overexpression of Bcl-2 and by cyclosporin A, implicating the involvement of the intrinsic apoptotic pathway. Selective inhibition of mixed lineage kinase (MLK), p38 or JNK does not attenuate the decrease in Akt phosphorylation showing that inactivation of the Akt pathway occurs independently of the MLK/MAPK pathway. Together, these results reveal that peroxynitrite-induced activation of the intrinsic apoptotic pathway involves interactions with the MLK/MAPK and Akt signaling pathways.
引用
收藏
页码:1506 / 1514
页数:8
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