Haustead Daniel J, Lukehurst Sherralee S, Clutton Genevieve T, Bartlett Carole A, Dunlop Sarah A, Arrese Catherine A, Sherrard Rachel M, Rodger Jennifer
School of Animal Biology, Faculty of Medicine and Dentistry, University of Western Australia, Crawley, WA 6009, Australia.
J Neurosci. 2008 Jul 16;28(29):7376-86. doi: 10.1523/JNEUROSCI.1135-08.2008.
Topographically ordered projections are established by molecular guidance cues and refined by neuronal activity. Retinal input to a primary visual center, the superior colliculus (SC), is bilateral with a dense contralateral projection and a sparse ipsilateral one. Both projections are topographically organized, but in opposing anterior-posterior orientations. This arrangement provides functionally coherent input to each colliculus from the binocular visual field, supporting visual function. When guidance cues involved in contralateral topography (ephrin-As) are absent, crossed retinal ganglion cell (RGC) axons form inappropriate terminations within the SC. However, the organization of the ipsilateral projection relative to the abnormal contralateral input remains unknown, as does the functional capacity of both projections. We show here that in ephrin-A(-/-) mice, the SC contains an expanded, diffuse ipsilateral projection. Electrophysiological recording demonstrated that topography of visually evoked responses recorded from the contralateral superior colliculus of ephrin-A(-/-) mice displayed similar functional disorder in all genotypes, contrasting with their different degrees of anatomical disorder. In contrast, ipsilateral responses were retinotopic in ephrin-A2(-/-) but disorganized in ephrin-A2/A5(-/-) mice. The lack of integration of binocular input resulted in specific visual deficits, which could be reversed by occlusion of one eye. The discrepancy between anatomical and functional topography in both the ipsilateral and contralateral projections implies suppression of inappropriately located terminals. Moreover, the misalignment of ipsilateral and contralateral visual information in ephrin-A2/A5(-/-) mice suggests a role for ephrin-As in integrating convergent visual inputs.
拓扑有序投射由分子引导线索建立,并通过神经元活动进行细化。视网膜向初级视觉中枢上丘(SC)的输入是双侧的,对侧投射密集,同侧投射稀疏。这两种投射都是按拓扑方式组织的,但前后方向相反。这种排列为每个上丘提供了来自双眼视野的功能连贯输入,支持视觉功能。当参与对侧拓扑结构的引导线索(ephrin-As)缺失时,交叉的视网膜神经节细胞(RGC)轴突会在上丘内形成不适当的终末。然而,同侧投射相对于异常对侧输入的组织情况仍然未知,这两种投射的功能能力也是如此。我们在此表明,在ephrin-A基因敲除小鼠中,上丘包含一个扩大的、弥散的同侧投射。电生理记录表明,从ephrin-A基因敲除小鼠对侧上丘记录到的视觉诱发反应的拓扑结构在所有基因型中都表现出类似的功能紊乱,这与它们不同程度的解剖学紊乱形成对比。相比之下,同侧反应在ephrin-A2基因敲除小鼠中是视网膜拓扑有序的,但在ephrin-A2/A5基因敲除小鼠中是紊乱的。双眼输入缺乏整合导致了特定的视觉缺陷,通过单眼遮挡可以逆转这种缺陷。同侧和对侧投射中解剖学和功能拓扑结构之间的差异意味着对位置不当的终末有抑制作用。此外,ephrin-A2/A5基因敲除小鼠中同侧和对侧视觉信息的错位表明ephrin-As在整合汇聚的视觉输入中起作用。