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两条不同的信号通路调节过氧亚硝酸盐诱导的PC12细胞凋亡。

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

作者信息

Shacka J J, Garner M A, Gonzalez J D, Ye Y-Z, D'Alessandro T L, Estévez A G

机构信息

Department of Physiology and Biophysics, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Cell Death Differ. 2006 Sep;13(9):1506-14. doi: 10.1038/sj.cdd.4401831. Epub 2006 Jan 20.

Abstract

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.

摘要

过氧亚硝酸盐诱导细胞凋亡的机制尚未完全明确。我们在此报告,过氧亚硝酸盐诱导PC12细胞凋亡需要同时激活p38和JNK丝裂原活化蛋白激酶(MAP激酶),进而激活内源性凋亡途径,这表现为Bax转位至线粒体、细胞色素c释放至细胞质以及半胱天冬酶的激活,最终导致细胞死亡。过氧亚硝酸盐会诱导Akt途径失活。此外,持续激活的Akt的过表达可抑制过氧亚硝酸盐诱导的Bax转位和细胞死亡。Bcl-2的过表达和环孢素A可阻止过氧亚硝酸盐诱导的细胞死亡,提示内源性凋亡途径参与其中。对混合谱系激酶(MLK)、p38或JNK的选择性抑制并不会减弱Akt磷酸化的降低,这表明Akt途径的失活独立于MLK/MAPK途径发生。总之,这些结果表明,过氧亚硝酸盐诱导的内源性凋亡途径的激活涉及与MLK/MAPK和Akt信号通路的相互作用。

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