粒体自噬
自噬
细胞生物学
线粒体
生物能学
生物发生
生物
线粒体生物发生
程序性细胞死亡
生物化学
细胞凋亡
基因
作者
Muriel Priault,Bénédicte Salin,Jacques Schaëffer,François M. Vallette,J-P di Rago,Jean‐Claude Martinou
标识
DOI:10.1038/sj.cdd.4401697
摘要
Autophagy, a highly regulated programme found in almost all eukaryotes, is mainly viewed as a catabolic process that degrades nonessential cellular components into molecular building blocks, subsequently available for biosynthesis at a lesser expense than de novo synthesis. Autophagy is largely known to be regulated by nutritional conditions. Here we show that, in yeast cells grown under nonstarving conditions, autophagy can be induced by mitochondrial dysfunction. Electron micrographs and biochemical studies show that an autophagic activity can result from impairing the mitochondrial electrochemical transmembrane potential. Furthermore, mitochondrial damage-induced autophagy results in the preferential degradation of impaired mitochondria (mitophagy), before leading to cell death. Mitophagy appears to rely on classical macroautophagy machinery while being independent of cellular ATP collapse. These results suggest that in this case, autophagy can be envisioned either as a process of mitochondrial quality control, or as an ultimate cellular response triggered when cells are overwhelmed with damaged mitochondria.
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