Cell signaling and mitochondrial dynamics: Implications for neuronal function and neurodegenerative disease

被引:50
|
作者
Wilson, Theodore J. [2 ]
Slupe, Andrew M. [1 ]
Strack, Stefan [1 ,2 ]
机构
[1] Univ Iowa, Dept Pharmacol, Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Mol & Cellular Biol Program, Carver Coll Med, Iowa City, IA 52242 USA
关键词
Mitochondrial fission; Mitochondrial fusion; Mitochondrial transport; Protein phosphorylation; Dynamin-related protein 1; Mitofusin; Optic atrophy 1; Neurodegeneration; Charcot-Marie-Tooth disease; Autosomal dominant optic atrophy; Synaptic transmission; Synaptogenesis; DEPENDENT PROTEIN-KINASE; DOMINANT OPTIC ATROPHY; CYTOCHROME-C RELEASE; KINESIN HEAVY-CHAIN; NITRIC-OXIDE; AXONAL-TRANSPORT; PINK1; FUNCTION; PEROXISOMAL FISSION; PARKINSONS-DISEASE; REGULATORY SUBUNIT;
D O I
10.1016/j.nbd.2012.01.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:13 / 26
页数:14
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