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神经元中TRAK介导的线粒体运输的发育变化。

Developmental changes in trak-mediated mitochondrial transport in neurons.

作者信息

Loss Omar, Stephenson F Anne

机构信息

School of Pharmacy University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom.

School of Pharmacy University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom.

出版信息

Mol Cell Neurosci. 2017 Apr;80:134-147. doi: 10.1016/j.mcn.2017.03.006. Epub 2017 Mar 11.

DOI:10.1016/j.mcn.2017.03.006
PMID:28300646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5400476/
Abstract

Previous studies established that the kinesin adaptor proteins, TRAK1 and TRAK2, play an important role in mitochondrial transport in neurons. They link mitochondria to kinesin motor proteins via a TRAK acceptor protein in the mitochondrial outer membrane, the Rho GTPase, Miro. TRAKs also associate with enzyme, O-linked N-acetylglucosamine transferase (OGT), to form a quaternary, mitochondrial trafficking complex. A recent report suggested that TRAK1 preferentially controls mitochondrial transport in axons of hippocampal neurons whereas TRAK2 controls mitochondrial transport in dendrites. However, it is not clear whether the function of any of these proteins is exclusive to axons or dendrites and if their mechanisms of action are conserved between different neuronal populations and also, during maturation. Here, a comparative study was carried out into TRAK-mediated mitochondrial mobility in axons and dendrites of hippocampal and cortical neurons during maturation in vitro using a shRNA gene knockdown approach. It was found that in mature hippocampal and cortical neurons, TRAK1 predominantly mediates axonal mitochondrial transport whereas dendritic transport is mediated via TRAK2. In young, maturing neurons, TRAK1 and TRAK2 contribute similarly in mitochondrial transport in both axons and dendrites in both neuronal types. These findings demonstrate maturation regulation of mitochondrial transport which is conserved between at least two distinct neuronal subtypes.

摘要

先前的研究表明,驱动蛋白衔接蛋白TRAK1和TRAK2在神经元的线粒体运输中发挥重要作用。它们通过线粒体外膜中的一种TRAK受体蛋白、Rho GTP酶Miro将线粒体与驱动蛋白运动蛋白相连。TRAKs还与O-连接的N-乙酰葡糖胺转移酶(OGT)结合,形成一个四级线粒体运输复合体。最近的一份报告表明,TRAK1优先控制海马神经元轴突中的线粒体运输,而TRAK2控制树突中的线粒体运输。然而,尚不清楚这些蛋白中的任何一种的功能是否仅限于轴突或树突,以及它们的作用机制在不同神经元群体之间以及在成熟过程中是否保守。在此,使用shRNA基因敲低方法,对体外成熟过程中海马神经元和皮质神经元轴突和树突中TRAK介导的线粒体移动性进行了一项比较研究。研究发现,在成熟的海马神经元和皮质神经元中,TRAK1主要介导轴突线粒体运输,而树突运输则由TRAK2介导。在年轻的、正在成熟的神经元中,TRAK1和TRAK2在两种神经元类型的轴突和树突中的线粒体运输中发挥相似的作用。这些发现证明了线粒体运输的成熟调节在至少两种不同的神经元亚型之间是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/c6cff54574c8/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/ab455b8aba36/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/a4e1ead190c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/d58efa0e7937/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/f2b6cbf917b2/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/4ebb62a8205f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/12d92dc78bc9/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/c6cff54574c8/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/ab455b8aba36/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/a4e1ead190c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/d58efa0e7937/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/f2b6cbf917b2/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/4ebb62a8205f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/12d92dc78bc9/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b3/5400476/c6cff54574c8/gr6.jpg

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