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兼职马达蛋白:驱动蛋白、动力蛋白与细胞极性

Moonlighting Motors: Kinesin, Dynein, and Cell Polarity.

作者信息

Lu Wen, Gelfand Vladimir I

机构信息

Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Avenue, Ward 11-100, Chicago, IL 60611, USA.

Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Avenue, Ward 11-100, Chicago, IL 60611, USA.

出版信息

Trends Cell Biol. 2017 Jul;27(7):505-514. doi: 10.1016/j.tcb.2017.02.005. Epub 2017 Mar 8.

DOI:10.1016/j.tcb.2017.02.005
PMID:28284467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5476484/
Abstract

In addition to their well-known role in transporting cargoes in the cytoplasm, microtubule motors organize their own tracks - the microtubules. While this function is mostly studied in the context of cell division, it is essential for microtubule organization and generation of cell polarity in interphase cells. Kinesin-1, the most abundant microtubule motor, plays a role in the initial formation of neurites. This review describes the mechanism of kinesin-1-driven microtubule sliding and discusses its biological significance in neurons. Recent studies describing the interplay between kinesin-1 and cytoplasmic dynein in the translocation of microtubules are discussed. In addition, we evaluate recent work exploring the developmental regulation of microtubule sliding during axonal outgrowth and regeneration. Collectively, the discussed works suggest that sliding of interphase microtubules by motors is a novel force-generating mechanism that reorganizes the cytoskeleton and drives shape change and polarization.

摘要

除了在细胞质中运输货物的众所周知的作用外,微管马达还能组织它们自己的轨道——微管。虽然这个功能大多是在细胞分裂的背景下研究的,但它对于间期细胞中微管的组织和细胞极性的产生至关重要。驱动蛋白-1是最丰富的微管马达,在神经突的初始形成中发挥作用。这篇综述描述了驱动蛋白-1驱动的微管滑动机制,并讨论了其在神经元中的生物学意义。还讨论了最近描述驱动蛋白-1和胞质动力蛋白在微管转运中相互作用的研究。此外,我们评估了最近探索轴突生长和再生过程中微管滑动的发育调控的工作。总体而言,所讨论的研究表明,马达驱动的间期微管滑动是一种新的力产生机制,可重组细胞骨架并驱动形状变化和极化。

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本文引用的文献

1
Neurite outgrowth is driven by actin polymerization even in the presence of actin polymerization inhibitors.即使存在肌动蛋白聚合抑制剂,神经突生长仍由肌动蛋白聚合驱动。
Mol Biol Cell. 2016 Sep 28;27(23):3695-704. doi: 10.1091/mbc.E16-04-0253.
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Role of kinesin-1-based microtubule sliding in Drosophila nervous system development.基于驱动蛋白-1的微管滑动在果蝇神经系统发育中的作用。
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Microtubule-microtubule sliding by kinesin-1 is essential for normal cytoplasmic streaming in Drosophila oocytes.驱动蛋白-1介导的微管-微管滑动对于果蝇卵母细胞中正常的细胞质流动至关重要。
Proc Natl Acad Sci U S A. 2016 Aug 23;113(34):E4995-5004. doi: 10.1073/pnas.1522424113. Epub 2016 Aug 10.
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Microtubules and Growth Cones: Motors Drive the Turn.微管与生长锥:分子马达驱动转向
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Sliding of centrosome-unattached microtubules defines key features of neuronal phenotype.中心体未附着微管的滑动定义了神经元表型的关键特征。
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Interplay between kinesin-1 and cortical dynein during axonal outgrowth and microtubule organization in Drosophila neurons.驱动蛋白-1与皮层动力蛋白在果蝇神经元轴突生长和微管组织过程中的相互作用。
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A novel isoform of MAP4 organises the paraxial microtubule array required for muscle cell differentiation.一种新型的微管相关蛋白4(MAP4)异构体组装肌肉细胞分化所需的近轴微管阵列。
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Drosophila CLIP-190 and mammalian CLIP-170 display reduced microtubule plus end association in the nervous system.果蝇CLIP-190和哺乳动物CLIP-170在神经系统中显示出微管正端结合减少。
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Mol Biol Cell. 2015 Apr 1;26(7):1296-307. doi: 10.1091/mbc.E14-10-1423. Epub 2015 Feb 5.