Smidt Heart Institute, Cedars-Sinai Medical Center, AHSP9313, 127 S. San Vicente Blvd., Los Angeles, CA, 90048, USA.
Cell Mol Life Sci. 2021 Apr;78(8):3791-3801. doi: 10.1007/s00018-021-03772-3. Epub 2021 Feb 5.
Mitochondrial quality control depends upon selective elimination of damaged mitochondria, replacement by mitochondrial biogenesis, redistribution of mitochondrial components across the network by fusion, and segregation of damaged mitochondria by fission prior to mitophagy. In this review, we focus on mitochondrial dynamics (fusion/fission), mitophagy, and other mechanisms supporting mitochondrial quality control including maintenance of mtDNA and the mitochondrial unfolded protein response, particularly in the context of the heart.
线粒体质量控制依赖于有选择地消除损伤的线粒体,通过线粒体生物发生来替换,通过融合在网络中重新分配线粒体成分,以及在自噬之前通过分裂来分离损伤的线粒体。在这篇综述中,我们专注于线粒体动力学(融合/分裂)、自噬以及支持线粒体质量控制的其他机制,包括 mtDNA 和线粒体未折叠蛋白反应的维持,特别是在心脏的背景下。