PARP and RIP-1 are required for autophagy induced by 11’-deoxyverticillin A, which precedes caspase-dependent apoptosis. ----中国科学院微生物研究所

科研成果

论文题目:	PARP and RIP-1 are required for autophagy induced by 11’-deoxyverticillin A, which precedes caspase-dependent apoptosis.
作者:	Nan Zhang, Yali Chen, Ruixuan Jiang, Erwei Li, Xiuling Chen, Zhijun Xi, Yinglu Guo, Xingzhong Liu, Yuguang Zhou, Yongsheng Che, Xuejun Jiang
联系作者:	车永胜，姜学军
刊物名称:	Autophagy
期:	6
卷:	7
页:	598-612
年份:	2011
影响因子:	6.643
论文下载:
摘要:	The epipolythiodioxopiperazines (ETPs) are fungal secondary metabolites proven to trigger both apoptotic and necrotic cell death of tumor cells. However, the underlying mechanism of their regulatory role in macroautophagy and the interplay between autophagy and apoptosis initiated by the ETPs, remain unexplored. In the current work, we found that 11'-deoxyverticillin A (C42), a member of the ETPs, induces autophagosome formation, accumulation of microtubule-associated protein 1 light chain 3-II (LC3-II ) and degradation of sequestosome 1 (SQSTM1/p62). In addition, the LC3-II accrual and p62 degradation occur prior to caspase activation and coincide with PARP activation. Inhibition of autophagy by either chemical inhibitors or by RNA interference single knockdown of essential autophagic genes partially reduces the cell death and the cleavage of both caspase 3 and PARP. Necrostatin-1, a specific inhibitor of necroptosis, inhibits both the augmentation of LC3-II and the cleavage of caspase 3, which was confirmed by depletion of receptor-interacting protein 1 (RIP-1), a crucial necrostatin-1-targeted adaptor kinase mediating cell death and survival. Moreover, inhibition of PARP by either chemical inhibitors or RNA interference provides obvious protection for cell viability and suppresses the LC3-II accretion caused by C42 treatment. Interestingly, double silencing of LC3 and p62 completely suppressed PARP cleavage and concurrently and maximally augmented the PAR formation induced by C42. Collectively, we have demonstrated that C42 enhances the cellular autophagic process, which requires both PARP and RIP-1 participation, preceding and possibly augmenting, the caspase-dependent apoptotic cell death.