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神经元极化中的信号网络。

Signaling networks in neuronal polarization.

作者信息

Yoshimura Takeshi, Arimura Nariko, Kaibuchi Kozo

机构信息

Department of Molecular Biology, Graduate School of Science, Institute for Advanced Research, Nagoya University, Aichi 464-8602, Japan.

出版信息

J Neurosci. 2006 Oct 18;26(42):10626-30. doi: 10.1523/JNEUROSCI.3824-06.2006.

DOI:10.1523/JNEUROSCI.3824-06.2006
PMID:17050700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6674748/
Abstract

A mature neuron is typically polarized both structurally and functionally, with a single long axon and several dendrites. Neuronal polarity is essential for unidirectional signal flow from somata or dendrites to axons. The initial event in establishing a polarized neuron is the specification of a single axon. Early in neuronal development, one immature neurite becomes differentiated from other neurites to form an axon. Although studies in the past two decades have yielded a catalog of structural, molecular, and functional differences between axons and dendrites, we are only now beginning to understand the molecular mechanisms involved in the establishment of neuronal polarity. In the last few years, neuronal polarity-regulating molecules have been revealed. There are two major signaling cascades in neuronal polarization. Several groups, including ours, reported that the phosphatidylinositol 3-kinase (PI3-kinase)/Akt/glycogen synthase kinase-3beta (GSK-3beta)/collapsin response mediator protein-2 pathway is important for axon specification and elongation. Recent studies have revealed that the positive feedback loop composed of Rho family small GTPases and the Par3/Par6/atypical protein kinase C complex plays a role in the initial events of neuronal polarization downstream of PI3-kinase. Here, we discuss the roles of signaling molecules for axon specification.

摘要

成熟神经元通常在结构和功能上都是极化的,具有单一的长轴突和多个树突。神经元极性对于从胞体或树突到轴突的单向信号流动至关重要。建立极化神经元的初始事件是确定单一轴突。在神经元发育早期,一条未成熟的神经突与其他神经突区分开来形成轴突。尽管过去二十年的研究已经列出了轴突和树突之间结构、分子和功能上的差异清单,但我们直到现在才开始了解参与建立神经元极性的分子机制。在过去几年中,已经发现了调节神经元极性的分子。在神经元极化中有两个主要的信号级联反应。包括我们小组在内的几个研究团队报告说,磷脂酰肌醇3激酶(PI3激酶)/Akt/糖原合酶激酶-3β(GSK-3β)/塌陷反应介导蛋白-2途径对于轴突的确定和延长很重要。最近的研究表明,由Rho家族小GTP酶和Par3/Par6/非典型蛋白激酶C复合物组成的正反馈环在PI3激酶下游的神经元极化初始事件中起作用。在这里,我们讨论信号分子在轴突确定中的作用。

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Signaling networks in neuronal polarization.神经元极化中的信号网络。
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2
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本文引用的文献

1
Transport of PIP3 by GAKIN, a kinesin-3 family protein, regulates neuronal cell polarity.驱动蛋白-3家族蛋白GAKIN对磷脂酰肌醇-3,4,5-三磷酸(PIP3)的转运调节神经元细胞极性。
J Cell Biol. 2006 Jul 31;174(3):425-36. doi: 10.1083/jcb.200604031. Epub 2006 Jul 24.
2
Requirement of dendritic Akt degradation by the ubiquitin-proteasome system for neuronal polarity.神经元极性形成中泛素-蛋白酶体系统对树突状Akt降解的需求。
J Cell Biol. 2006 Jul 31;174(3):415-24. doi: 10.1083/jcb.200511028. Epub 2006 Jul 24.
3
A change in the selective translocation of the Kinesin-1 motor domain marks the initial specification of the axon.驱动蛋白-1运动结构域选择性易位的变化标志着轴突的初始特化。
Neuron. 2006 Mar 16;49(6):797-804. doi: 10.1016/j.neuron.2006.02.005.
4
Ras regulates neuronal polarity via the PI3-kinase/Akt/GSK-3beta/CRMP-2 pathway.Ras通过磷脂酰肌醇-3激酶/蛋白激酶B/糖原合成酶激酶-3β/ collapsin反应调节蛋白-2途径调控神经元极性。
Biochem Biophys Res Commun. 2006 Feb 3;340(1):62-8. doi: 10.1016/j.bbrc.2005.11.147. Epub 2005 Dec 6.
5
Phosphorylation by Rho kinase regulates CRMP-2 activity in growth cones.Rho激酶介导的磷酸化作用调节生长锥中CRMP-2的活性。
Mol Cell Biol. 2005 Nov;25(22):9973-84. doi: 10.1128/MCB.25.22.9973-9984.2005.
6
CRMP-2 is involved in kinesin-1-dependent transport of the Sra-1/WAVE1 complex and axon formation.CRMP-2参与Sra-1/WAVE1复合体的驱动蛋白1依赖性运输及轴突形成。
Mol Cell Biol. 2005 Nov;25(22):9920-35. doi: 10.1128/MCB.25.22.9920-9935.2005.
7
Tubulin and CRMP-2 complex is transported via Kinesin-1.微管蛋白与CRMP-2复合物通过驱动蛋白-1进行运输。
J Neurochem. 2005 Jun;93(6):1371-82. doi: 10.1111/j.1471-4159.2005.03063.x.
8
Glycogen synthase kinase-3beta phosphorylation of MAP1B at Ser1260 and Thr1265 is spatially restricted to growing axons.糖原合酶激酶-3β在丝氨酸1260和苏氨酸1265位点对微管相关蛋白1B的磷酸化作用在空间上局限于正在生长的轴突。
J Cell Sci. 2005 Mar 1;118(Pt 5):993-1005. doi: 10.1242/jcs.01697.
9
PAR-6-PAR-3 mediates Cdc42-induced Rac activation through the Rac GEFs STEF/Tiam1.PAR-6与PAR-3通过Rac鸟嘌呤核苷酸交换因子(GEF)STEF/Tiam1介导Cdc42诱导的Rac激活。
Nat Cell Biol. 2005 Mar;7(3):270-7. doi: 10.1038/ncb1227. Epub 2005 Feb 20.
10
GSK-3beta regulates phosphorylation of CRMP-2 and neuronal polarity.糖原合成酶激酶-3β调节CRMP-2的磷酸化及神经元极性。
Cell. 2005 Jan 14;120(1):137-49. doi: 10.1016/j.cell.2004.11.012.