Dorn Gerald W
From the Department of Internal Medicine, Center for Pharmacogenomics, Washington University School of Medicine, St. Louis, MO.
Circ Res. 2015 Jan 16;116(2):225-8. doi: 10.1161/CIRCRESAHA.114.305672.
Mitochondrial fission and fusion proteins are highly expressed in myocardium. However, mitochondrial fission and fusion are rare, and mitochondrial networks are absent, in adult cardiomyocytes, obviating a need for morphometric mitochondrial remodeling. The critical role of mitochondrial dynamics factors in hearts therefore remains to be determined. In this issue of Ikeda et al describe a central function for the mitochondrial fission protein, Dynamin-related protein 1 (Drp-1), in macroautophagy and mitochondrial autophagy. Together with two other recent reports that cardiac-specific deletion of Drp1 perturbs mitophagy, these findings point to modulation of targeted mitochondrial elimination as a major quality control function for Drp1, and possible other mitochondrial dynamism factors, in the heart.
线粒体分裂和融合蛋白在心肌中高度表达。然而,在成年心肌细胞中,线粒体分裂和融合很少见,并且不存在线粒体网络,因此无需进行形态计量学的线粒体重塑。因此,线粒体动力学因子在心脏中的关键作用仍有待确定。在本期杂志中,池田等人描述了线粒体分裂蛋白动力相关蛋白1(Drp-1)在巨自噬和线粒体自噬中的核心功能。连同最近另外两篇关于心脏特异性缺失Drp1会扰乱线粒体自噬的报道,这些发现表明,靶向线粒体清除的调节是Drp1以及心脏中可能的其他线粒体动力学因子的主要质量控制功能。