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神经细胞黏附分子(Nr-CAM)在双眼视觉通路模式形成中的作用。

A role for Nr-CAM in the patterning of binocular visual pathways.

作者信息

Williams Scott E, Grumet Martin, Colman David R, Henkemeyer Mark, Mason Carol A, Sakurai Takeshi

机构信息

Center for Neurobiology and Behavior and Department of Pathology, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.

出版信息

Neuron. 2006 May 18;50(4):535-47. doi: 10.1016/j.neuron.2006.03.037.

Abstract

Retinal ganglion cell (RGC) axons diverge within the optic chiasm to project to opposite sides of the brain. In mouse, contralateral RGCs are distributed throughout the retina, whereas ipsilateral RGCs are restricted to the ventrotemporal crescent (VTC). While repulsive guidance mechanisms play a major role in the formation of the ipsilateral projection, little is known about the contribution of growth-promoting interactions to the formation of binocular visual projections. Here, we show that the cell adhesion molecule Nr-CAM is expressed by RGCs that project contralaterally and is critical for the guidance of late-born RGCs within the VTC. Blocking Nr-CAM function causes an increase in the size of the ipsilateral projection and reduces neurite outgrowth on chiasm cells in an age- and region-specific manner. Finally, we demonstrate that EphB1/ephrin-B2-mediated repulsion and Nr-CAM-mediated attraction comprise distinct molecular programs that each contributes to the proper formation of binocular visual pathways.

摘要

视网膜神经节细胞(RGC)轴突在视交叉内发散,投射到脑的对侧。在小鼠中,对侧RGC分布于整个视网膜,而同侧RGC局限于颞腹侧新月区(VTC)。虽然排斥性导向机制在同侧投射的形成中起主要作用,但关于促进生长的相互作用对双眼视觉投射形成的贡献知之甚少。在此,我们表明细胞粘附分子Nr-CAM由对侧投射的RGC表达,并且对VTC内晚期生成的RGC的导向至关重要。阻断Nr-CAM功能会导致同侧投射的大小增加,并以年龄和区域特异性方式减少视交叉细胞上的神经突生长。最后,我们证明EphB1/ephrin-B2介导的排斥和Nr-CAM介导的吸引包含不同的分子程序,它们各自有助于双眼视觉通路的正确形成。

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