Inatani Masaru
Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, 1-1-1 Honjo, Kumamoto 860-8556, Japan.
Naturwissenschaften. 2005 Dec;92(12):549-61. doi: 10.1007/s00114-005-0042-5. Epub 2005 Oct 12.
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.
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。