EA4576, Maladies Rares: Génétique et Métabolisme, 33000 Bordeaux Cedex, France.
Cell Metab. 2013 May 7;17(5):719-30. doi: 10.1016/j.cmet.2013.03.014. Epub 2013 Apr 18.
Mitophagy has been recently described as a mechanism of elimination of damaged organelles. Although the regulation of the amount of mitochondria is a core issue concerning cellular energy homeostasis, the relationship between mitochondrial degradation and energetic activity has not yet been considered. Here, we report that the stimulation of mitochondrial oxidative phosphorylation enhances mitochondrial renewal by increasing its degradation rate. Upon high oxidative phosphorylation activity, we found that the small GTPase Rheb is recruited to the mitochondrial outer membrane. This mitochondrial localization of Rheb promotes mitophagy through a physical interaction with the mitochondrial autophagic receptor Nix and the autophagosomal protein LC3-II. Thus, Rheb-dependent mitophagy contributes to the maintenance of optimal mitochondrial energy production. Our data suggest that mitochondrial degradation contributes to a bulk renewal of the organelle in order to prevent mitochondrial aging and to maintain the efficiency of oxidative phosphorylation.
自噬最近被描述为一种消除受损细胞器的机制。虽然线粒体数量的调节是涉及细胞能量稳态的核心问题,但线粒体降解与能量活性之间的关系尚未得到考虑。在这里,我们报告说,刺激线粒体氧化磷酸化通过增加其降解速率来增强线粒体的更新。在高氧化磷酸化活性下,我们发现小分子 GTP 酶 Rheb 被募集到线粒体的外膜上。这种 Rheb 的线粒体定位通过与线粒体自噬受体 Nix 和自噬体蛋白 LC3-II 的物理相互作用促进了自噬。因此,Rheb 依赖性自噬有助于维持最佳的线粒体能量产生。我们的数据表明,线粒体降解有助于细胞器的大量更新,以防止线粒体衰老并维持氧化磷酸化的效率。