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线粒体通过局部轴内蛋白合成协调轴突分支位点。

Mitochondria coordinate sites of axon branching through localized intra-axonal protein synthesis.

机构信息

Department of Anatomy and Cell Biology, Shriners Hospitals Pediatric Research Center, Temple University, 3500 North Broad Street, Philadelphia, PA 19140, USA.

Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA 19210, USA.

出版信息

Cell Rep. 2013 Dec 26;5(6):1564-75. doi: 10.1016/j.celrep.2013.11.022. Epub 2013 Dec 12.


DOI:10.1016/j.celrep.2013.11.022
PMID:24332852
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3947524/
Abstract

The branching of axons is a fundamental aspect of nervous system development and neuroplasticity. We report that branching of sensory axons in the presence of nerve growth factor (NGF) occurs at sites populated by stalled mitochondria. Translational machinery targets to presumptive branching sites, followed by recruitment of mitochondria to these sites. The mitochondria promote branching through ATP generation and the determination of localized hot spots of active axonal mRNA translation, which contribute to actin-dependent aspects of branching. In contrast, mitochondria do not have a role in the regulation of the microtubule cytoskeleton during NGF-induced branching. Collectively, these observations indicate that sensory axons exhibit multiple potential sites of translation, defined by presence of translational machinery, but active translation occurs following the stalling and respiration of mitochondria at these potential sites of translation. This study reveals a local role for axonal mitochondria in the regulation of the actin cytoskeleton and axonal mRNA translation underlying branching.

摘要

轴突的分支是神经系统发育和神经可塑性的一个基本方面。我们报告说,在神经生长因子 (NGF) 的存在下,感觉轴突的分支发生在停滞的线粒体所在的部位。翻译机制靶向假定的分支部位,然后招募线粒体到这些部位。线粒体通过产生 ATP 和确定局部活跃的 mRNA 翻译热点来促进分支,这有助于分支的肌动蛋白依赖性方面。相比之下,线粒体在 NGF 诱导的分支过程中对微管细胞骨架的调节没有作用。总的来说,这些观察结果表明,感觉轴突表现出多个潜在的翻译部位,由翻译机制定义,但在这些潜在的翻译部位,线粒体的停滞和呼吸后,才会发生活跃的翻译。这项研究揭示了轴突线粒体在调节分支所涉及的肌动蛋白细胞骨架和轴突 mRNA 翻译中的局部作用。

相似文献

[1]
Mitochondria coordinate sites of axon branching through localized intra-axonal protein synthesis.

Cell Rep. 2013-12-12

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Neuronal development: SAD kinases make happy axons.

Curr Biol. 2013-9-9

[2]
Motile axonal mitochondria contribute to the variability of presynaptic strength.

Cell Rep. 2013-7-25

[3]
RNA-binding protein Vg1RBP regulates terminal arbor formation but not long-range axon navigation in the developing visual system.

Dev Neurobiol. 2014-3

[4]
Terminal axon branching is regulated by the LKB1-NUAK1 kinase pathway via presynaptic mitochondrial capture.

Cell. 2013-6-20

[5]
RNA-binding protein Hermes/RBPMS inversely affects synapse density and axon arbor formation in retinal ganglion cells in vivo.

J Neurosci. 2013-6-19

[6]
RNA-binding proteins and translational regulation in axons and growth cones.

Front Neurosci. 2013-5-23

[7]
Axonally synthesized β-actin and GAP-43 proteins support distinct modes of axonal growth.

J Neurosci. 2013-2-20

[8]
Vesicular glycolysis provides on-board energy for fast axonal transport.

Cell. 2013-1-31

[9]
Mechanisms underlying the initiation and dynamics of neuronal filopodia: from neurite formation to synaptogenesis.

Int Rev Cell Mol Biol. 2013

[10]
Nerve growth factor-induced formation of axonal filopodia and collateral branches involves the intra-axonal synthesis of regulators of the actin-nucleating Arp2/3 complex.

J Neurosci. 2012-12-5

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