The somal patterning of the AII amacrine cell mosaic in the mouse retina is indistinguishable from random simulations matched for density and constrained by soma size.

IF 1.1 4区 医学 Q4 NEUROSCIENCES Visual Neuroscience Pub Date : 2018-01-01 DOI:10.1017/S0952523817000347
Patrick W Keeley, Benjamin E Reese
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引用次数: 8

Abstract

The orderly spacing of retinal neurons is commonly regarded as a characteristic feature of retinal nerve cell populations. Exemplars of this property include the horizontal cells and the cholinergic amacrine cells, where individual cells minimize the proximity to like-type neighbors, yielding regularity in the patterning of their somata. Recently, two types of retinal bipolar cells in the mouse retina were shown to exhibit an order in their somal patterning no different from density-matched simulations constrained by soma size but being otherwise randomly distributed. The present study has now extended this finding to a type of retinal amacrine cell, the AII amacrine cell. Voronoi domain analysis revealed the patterning in the population of AII amacrine somata to be no different from density-matched and soma-size-constrained random simulations, while analysis of the density recovery profile showed AII amacrine cells to exhibit a minimal intercellular spacing identical to that for those random simulations: AII amacrine somata were positioned side-by-side as often as chance would predict. Regularity indexes and packing factors (PF) were far lower than those achieved by either the horizontal cells or cholinergic amacrine cells, with PFs also being comparable to those derived from the constrained random simulations. These results extend recent findings that call into question the widespread assumption that all types of retinal neurons are assembled as regular somal arrays, and have implications for the way in which AII amacrine cells must distribute their processes to ensure a uniform coverage of the retinal surface.

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小鼠视网膜中AII无突细胞马赛克的染色体模式与随机模拟的密度匹配和受体细胞大小的限制难以区分。
视网膜神经元的有序间隔通常被认为是视网膜神经细胞群的一个特征。这种特性的例子包括水平细胞和胆碱能无分泌细胞,其中单个细胞最大限度地减少了与同类邻居的接近,从而使它们的躯体模式具有规律性。最近,两种类型的视网膜双极细胞在小鼠视网膜上显示出一个顺序,在他们的染色体模式没有不同的密度匹配模拟受限制的体大小,但在其他方面随机分布。目前的研究已经将这一发现扩展到一种视网膜无突细胞,AII无突细胞。Voronoi结构域分析揭示了aiamacrine体细胞群体的模式与密度匹配和体细胞大小限制的随机模拟没有什么不同,而密度恢复剖面的分析显示aiamacrine细胞表现出最小的细胞间距,与那些随机模拟相同:aiamacrine体细胞并排排列的频率与机会预测的一样。规则指数和填充因子(PF)远低于水平细胞或胆碱能无分泌细胞的结果,PF也与约束随机模拟的结果相当。这些结果扩展了最近的一些发现,这些发现对广泛存在的假设提出了质疑,即所有类型的视网膜神经元都是按照规则的染色体阵列组装的,并对AII无突细胞必须分布其过程以确保视网膜表面均匀覆盖的方式产生了影响。
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来源期刊
Visual Neuroscience
Visual Neuroscience 医学-神经科学
CiteScore
2.20
自引率
5.30%
发文量
8
审稿时长
>12 weeks
期刊介绍: Visual Neuroscience is an international journal devoted to the publication of experimental and theoretical research on biological mechanisms of vision. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of all aspects of neuroscience research relating to the visual system. Contributions may address molecular, cellular or systems-level processes in either vertebrate or invertebrate species. The journal publishes work based on a wide range of technical approaches, including molecular genetics, anatomy, physiology, psychophysics and imaging, and utilizing comparative, developmental, theoretical or computational approaches to understand the biology of vision and visuo-motor control. The journal also publishes research seeking to understand disorders of the visual system and strategies for restoring vision. Studies based exclusively on clinical, psychophysiological or behavioral data are welcomed, provided that they address questions concerning neural mechanisms of vision or provide insight into visual dysfunction.
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