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Impairing the bioenergetic status and the biogenesis of mitochondria triggers mitophagy in yeast

机译:破坏线粒体的生物能状态和生物发生会触发酵母中的细胞吞噬

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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.
机译:自噬是几乎在所有真核生物中都受到严格控制的程序,主要被视为分解代谢过程,该过程将非必需的细胞成分降解为分子构件,随后可用于生物合成,而费用要比从头合成低。自噬在很大程度上受营养条件的调节。在这里,我们表明,在非饥饿条件下生长的酵母细胞中,线粒体功能障碍可以诱导自噬。电子显微照片和生化研究表明,自噬活性可能是由于线粒体的电化学跨膜电位受损所致。此外,线粒体损伤诱导的自噬导致受损的线粒体(线粒体)优先降解,从而导致细胞死亡。线粒体似乎依赖于经典的巨自噬机制,而与细胞ATP崩​​溃无关。这些结果表明,在这种情况下,自噬可以被认为是线粒体质量控制的过程,或者是当细胞被损坏的线粒体淹没时触发的最终细胞反应。

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