Department of Molecular and Cellular Biology Program, University of Iowa, Carver College of Medicine, Iowa City 52242, IA, USA.
Neurobiol Dis. 2013 Mar;51:13-26. doi: 10.1016/j.nbd.2012.01.009. Epub 2012 Jan 24.
Nascent evidence indicates that mitochondrial fission, fusion, and transport are subject to intricate regulatory mechanisms that intersect with both well-characterized and emerging signaling pathways. While it is well established that mutations in components of the mitochondrial fission/fusion machinery can cause neurological disorders, relatively little is known about upstream regulators of mitochondrial dynamics and their role in neurodegeneration. Here, we review posttranslational regulation of mitochondrial fission/fusion enzymes, with particular emphasis on dynamin-related protein 1 (Drp1), as well as outer mitochondrial signaling complexes involving protein kinases and phosphatases. We also review recent evidence that mitochondrial dynamics has profound consequences for neuronal development and synaptic transmission and discuss implications for clinical translation.
新兴证据表明,线粒体的分裂、融合和运输受到复杂的调控机制的影响,这些机制与已充分研究的和新兴的信号通路相互交叉。虽然线粒体分裂/融合机制的成分发生突变会导致神经紊乱已得到充分证实,但对于线粒体动力学的上游调节因子及其在神经退行性变中的作用却知之甚少。在这里,我们综述了线粒体分裂/融合酶的翻译后调控,特别强调了与蛋白激酶和磷酸酶有关的动力相关蛋白 1(Drp1)和线粒体外部信号复合物。我们还综述了最近的证据,表明线粒体动力学对神经元发育和突触传递有深远的影响,并讨论了其对临床转化的意义。