Tsai Pei-I, Papakyrikos Amanda M, Hsieh Chung-Han, Wang Xinnan
Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305.
Graduate Program in Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305.
Mol Biol Cell. 2017 Nov 15;28(24):3471-3479. doi: 10.1091/mbc.E17-03-0177. Epub 2017 Sep 13.
MIC60/mitofilin constitutes a hetero-oligomeric complex on the inner mitochondrial membranes to maintain crista structure. However, little is known about its physiological functions. Here, by characterizing mutants, we define its roles in vivo. We discover that performs dual functions to maintain mitochondrial homeostasis. In addition to its canonical role in crista membrane structure, MIC60 regulates mitochondrial motility, likely by influencing protein levels of the outer mitochondrial membrane protein Miro that anchors mitochondria to the microtubule motors. Loss of MIC60 causes loss of Miro and mitochondrial arrest. At a cellular level, loss of MIC60 disrupts synaptic structure and function at the neuromuscular junctions. The dual roles of MIC60 in both mitochondrial crista structure and motility position it as a crucial player for cellular integrity and survival.
MIC60/线粒体丝状蛋白在线粒体内膜上构成一个异源寡聚复合物以维持嵴的结构。然而,对其生理功能却知之甚少。在此,通过对突变体进行表征,我们确定了它在体内的作用。我们发现它具有维持线粒体稳态的双重功能。除了在嵴膜结构中的典型作用外,MIC60还可能通过影响线粒体外膜蛋白Miro的蛋白质水平来调节线粒体的运动,Miro将线粒体锚定到微管马达上。MIC60的缺失会导致Miro的缺失和线粒体停滞。在细胞水平上,MIC60的缺失会破坏神经肌肉接头处的突触结构和功能。MIC60在线粒体嵴结构和运动方面的双重作用使其成为细胞完整性和存活的关键参与者。