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本文引用的文献

1
Signaling from axon guidance receptors.轴突导向受体的信号传递。
Cold Spring Harb Perspect Biol. 2010 May;2(5):a001941. doi: 10.1101/cshperspect.a001941. Epub 2010 Mar 24.
2
Initiating and growing an axon.起始并生长轴突。
Cold Spring Harb Perspect Biol. 2010 Apr;2(4):a001925. doi: 10.1101/cshperspect.a001925.
3
RalA and the exocyst complex influence neuronal polarity through PAR-3 and aPKC.RalA和外泌体复合物通过PAR-3和非典型蛋白激酶C影响神经元极性。
J Cell Sci. 2009 May 15;122(Pt 10):1499-506. doi: 10.1242/jcs.044339. Epub 2009 Apr 21.
4
Different requirement for Rnd GTPases of R-Ras GAP activity of Plexin-C1 and Plexin-D1.Plexin-C1和Plexin-D1的R-Ras GAP活性对Rnd GTP酶的不同需求。
J Biol Chem. 2009 Mar 13;284(11):6743-51. doi: 10.1074/jbc.M805213200. Epub 2009 Jan 9.
5
Inhibition of Rac by the GAP activity of centralspindlin is essential for cytokinesis.中央纺锤体蛋白的GAP活性对Rac的抑制作用对于胞质分裂至关重要。
Science. 2008 Dec 5;322(5907):1543-6. doi: 10.1126/science.1163086.
6
The role of the cytoskeleton during neuronal polarization.细胞骨架在神经元极化过程中的作用。
Curr Opin Neurobiol. 2008 Oct;18(5):479-87. doi: 10.1016/j.conb.2008.09.019. Epub 2008 Oct 25.
7
Rheb and mTOR regulate neuronal polarity through Rap1B.Rheb和mTOR通过Rap1B调节神经元极性。
J Biol Chem. 2008 Nov 28;283(48):33784-92. doi: 10.1074/jbc.M802431200. Epub 2008 Oct 8.
8
Role of RhoA in activity-dependent cortical axon branching.RhoA在活动依赖性皮质轴突分支中的作用。
J Neurosci. 2008 Sep 10;28(37):9117-21. doi: 10.1523/JNEUROSCI.1731-08.2008.
9
Rac1 in cortical projection neurons is selectively required for midline crossing of commissural axonal formation.大脑皮质投射神经元中的Rac1蛋白是连合轴突形成过程中中线交叉所选择性必需的。
Eur J Neurosci. 2008 Jul;28(2):257-67. doi: 10.1111/j.1460-9568.2008.06343.x.
10
The role of Kalirin9 in p75/nogo receptor-mediated RhoA activation in cerebellar granule neurons.卡里林9在小脑颗粒神经元中p75/髓鞘相关糖蛋白受体介导的RhoA激活中的作用。
J Biol Chem. 2008 Sep 5;283(36):24690-7. doi: 10.1074/jbc.M802188200. Epub 2008 Jul 14.

Rho 和 Ras GTPases 在轴突生长、导向和分支中的作用。

Rho and Ras GTPases in axon growth, guidance, and branching.

机构信息

Memorial Sloan-Kettering Cancer Center, Cell Biology Program, New York, New York 10065, USA.

出版信息

Cold Spring Harb Perspect Biol. 2010 Feb;2(2):a001818. doi: 10.1101/cshperspect.a001818.

DOI:10.1101/cshperspect.a001818
PMID:20182621
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2828272/
Abstract

The establishment of precise neuronal cell morphology provides the foundation for all aspects of neurobiology. During development, axons emerge from cell bodies after an initial polarization stage, elongate, and navigate towards target regions guided by a range of environmental cues. The Rho and Ras families of small GTPases have emerged as critical players at all stages of axonogenesis. Their ability to coordinately direct multiple signal transduction pathways with precise spatial control drives many of the activities that underlie this morphogenetic program: the dynamic assembly, disassembly, and reorganization of the actin and microtubule cytoskeletons, the interaction of the growing axon with other cells and extracellular matrix, the delivery of lipids and proteins to the axon through the exocytic machinery, and the internalization of membrane and proteins at the leading edge of the growth cone through endocytosis. This article highlights the contribution of Rho and Ras GTPases to axonogenesis.

摘要

精确的神经元形态结构的建立为神经生物学的各个方面提供了基础。在发育过程中,轴突在初始极化阶段后从细胞体中伸出,延伸并在一系列环境线索的引导下向靶区导航。Rho 和 Ras 家族的小 GTP 酶已成为轴突发生的所有阶段的关键参与者。它们能够协调指导多个信号转导途径,并具有精确的空间控制,从而驱动许多构成这种形态发生程序的活动:肌动蛋白和微管细胞骨架的动态组装、拆卸和重组,生长轴突与其他细胞和细胞外基质的相互作用,通过胞吐机制将脂质和蛋白质输送到轴突中,以及通过内吞作用在生长锥的前缘内化膜和蛋白质。本文强调了 Rho 和 Ras GTP 酶对轴突发生的贡献。