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视神经轴突导向的分子机制。

Molecular mechanisms of optic axon guidance.

作者信息

Inatani Masaru

机构信息

Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, 1-1-1 Honjo, Kumamoto 860-8556, Japan.

出版信息

Naturwissenschaften. 2005 Dec;92(12):549-61. doi: 10.1007/s00114-005-0042-5. Epub 2005 Oct 12.

DOI:10.1007/s00114-005-0042-5
PMID:16220285
Abstract

Axon guidance is one of the critical processes during vertebrate central nervous system (CNS) development. The optic nerve, which contains the axons of retinal ganglion cells, has been used as a powerful model to elucidate some of the mechanisms underlying axon guidance because it is easily manipulated experimentally, and its function is well understood. Recent molecular biology studies have revealed that numerous guidance molecules control the development of the visual pathway. This review introduces the molecular mechanisms involved in each critical step during optic axon guidance. Axonal projections to the optic disc are thought to depend on adhesion molecules and inhibitory extracellular matrices such as chondroitin sulfate. The formation of the head of the optic nerve and the optic chiasm require ligand-receptor interactions between netrin-1 and the deleted in colorectal cancer receptor, and Slit proteins and Robo receptors, respectively. The gradient distributions of ephrin ligands and Eph receptors are essential for correct ipsilateral projections at the optic chiasm and the topographic mapping of axons in the superior colliculus/optic tectum. The precise gradient is regulated by transcription factors determining the retinal dorso-ventral and nasal-temporal polarities. Moreover, the axon guidance activities by Slit and semaphorin 5A require the existence of heparan sulfate, which binds to numerous guidance molecules. Recent discoveries about the molecular mechanisms underlying optic nerve guidance will facilitate progress in CNS developmental biology and axon-regeneration therapy.

摘要

轴突导向是脊椎动物中枢神经系统(CNS)发育过程中的关键步骤之一。视神经包含视网膜神经节细胞的轴突,由于其易于进行实验操作且功能已被充分了解,因此一直被用作阐明轴突导向潜在机制的有力模型。最近的分子生物学研究表明,众多导向分子控制着视觉通路的发育。本综述介绍了视神经轴突导向过程中每个关键步骤所涉及的分子机制。轴突向视盘的投射被认为依赖于黏附分子和抑制性细胞外基质,如硫酸软骨素。视神经头部和视交叉的形成分别需要netrin-1与结直肠癌缺失受体之间以及Slit蛋白与Robo受体之间的配体-受体相互作用。ephrin配体和Eph受体的梯度分布对于视交叉处正确的同侧投射以及上丘/视顶盖中轴突的拓扑映射至关重要。精确的梯度由决定视网膜背腹侧和鼻颞侧极性的转录因子调节。此外,Slit和信号素5A的轴突导向活性需要硫酸乙酰肝素的存在,硫酸乙酰肝素可与众多导向分子结合。关于视神经导向潜在分子机制的最新发现将促进中枢神经系统发育生物学和轴突再生治疗的进展。

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本文引用的文献

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Semaphorin 5A is a bifunctional axon guidance cue regulated by heparan and chondroitin sulfate proteoglycans.信号素5A是一种由硫酸乙酰肝素和硫酸软骨素蛋白聚糖调节的双功能轴突导向因子。
Neuron. 2004 Dec 16;44(6):961-75. doi: 10.1016/j.neuron.2004.12.002.
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Axon sorting in the optic tract requires HSPG synthesis by ext2 (dackel) and extl3 (boxer).视束中的轴突分选需要ext2(达克埃尔)和extl3(拳击手)合成硫酸乙酰肝素蛋白聚糖。
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高效的光子线索可用于排斥性轴突导向。
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Heparan sulfate regulates intraretinal axon pathfinding by retinal ganglion cells.硫酸乙酰肝素调控视网膜神经节细胞的视网膜内轴突寻路。
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Concerted action of CB1 cannabinoid receptor and deleted in colorectal cancer in axon guidance.CB1 大麻素受体与结肠癌缺失基因在神经轴突导向中的协同作用。
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Development of the retina and optic pathway.视网膜和视路的发育。
Vision Res. 2011 Apr 13;51(7):613-32. doi: 10.1016/j.visres.2010.07.010. Epub 2010 Jul 18.
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Foxd1 is required for proper formation of the optic chiasm.视交叉的正常形成需要Foxd1。
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J Neurosci. 2004 May 26;24(21):4989-99. doi: 10.1523/JNEUROSCI.4390-03.2004.
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Axonal heparan sulfate proteoglycans regulate the distribution and efficiency of the repellent slit during midline axon guidance.轴突硫酸乙酰肝素蛋白聚糖在中线轴突导向过程中调节排斥性分子Slit的分布和效能。
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Loss-of-function analysis of EphA receptors in retinotectal mapping.视网膜顶盖图谱中EphA受体的功能丧失分析。
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Differential sulfations and epimerization define heparan sulfate specificity in nervous system development.硫酸化差异和差向异构作用决定了神经系统发育过程中硫酸乙酰肝素的特异性。
Neuron. 2004 Mar 4;41(5):723-36. doi: 10.1016/s0896-6273(04)00084-4.
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Heparan sulfate proteoglycan syndecan promotes axonal and myotube guidance by slit/robo signaling.硫酸乙酰肝素蛋白聚糖syndecan通过slit/robo信号通路促进轴突和肌管导向。
Curr Biol. 2004 Feb 3;14(3):225-30. doi: 10.1016/j.cub.2004.01.006.