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视网膜神经节细胞树突结构与突触连接的发育

Development of Retinal Ganglion Cell Dendritic Structure and Synaptic Connections

作者信息

Tian Ning

机构信息

Associate Professor of Ophthalmology and Neurobiology, Moran Eye Center, University of Utah School of Medicine.

Abstract

The neuronal information of the visual scene that is processed by the retina is conducted to the brain by a set of separate spatio-temporal synaptic pathways. The morphological basis for the formation of these parallel synaptic pathways is the laminar-specific structure of the retina, in which specific subtypes of retinal neurons form synapses only with highly selective presynaptic and postsynaptic cells (1-3). Retinal ganglion cells (RGCs) are the output neurons of the retina. In the retina, RGCs synapse with bipolar and amacrine cells in the inner plexiform layer (IPL) to receive excitatory and inhibitory synaptic inputs respectively. The axons of RGCs travel through the optic nerve to retinorecipient structures in the brain, where they transfer their specific aspects of visual information to the higher centers (3). Because different subtypes of bipolar cells (Fig 1) (4) and amacrine cells (Fig. 2) (5) have their axonal/dendritic terminals in the specific sublaminae of the IPL, it is crucial that dendrites of individual RGCs are also confined to specific strata in order to synapses with them. Thus, the synaptic circuitries processing distinct visual features, the so called “parallel pathways” (1, 2, 6-10), start in the retina. In most mammals, RGCs can be divided into about 20 morphological subtypes based on their distinctive dendritic structure and synaptic connections (11-19). The wholemount drawings of mouse RGCs (Fig. 3) illustrate the diversity of morphologies present in mammalian RGCs ((19). See also RGCs of human, cat and rabbit retinas in the ganglion cell chapter in Webvision). Most of these RGCs have specific dendritic distribution in the IPL in adult retina as exemplified by the schematic (Fig. 4) showing the branching patterns of mouse RGCs. In most mammals, these lamina-restricted distributions of RGC dendrites and synaptic connections are formed during pre- and post-natal development. The question is how this lamination arises.

摘要

视网膜处理的视觉场景的神经元信息通过一组独立的时空突触通路传导至大脑。这些平行突触通路形成的形态学基础是视网膜的层特异性结构,其中特定亚型的视网膜神经元仅与高度选择性的突触前和突触后细胞形成突触(1-3)。视网膜神经节细胞(RGCs)是视网膜的输出神经元。在视网膜中,RGCs在内网状层(IPL)与双极细胞和无长突细胞形成突触,分别接受兴奋性和抑制性突触输入。RGCs的轴突穿过视神经到达大脑中的视网膜接受结构,在那里它们将视觉信息的特定方面传递到更高的中枢(3)。由于不同亚型的双极细胞(图1)(4)和无长突细胞(图2)(5)在IPL的特定亚层中有其轴突/树突末端,因此单个RGCs的树突也必须局限于特定层才能与它们形成突触,这一点至关重要。因此,处理不同视觉特征的突触回路,即所谓的“平行通路”(1,2,6-10),始于视网膜。在大多数哺乳动物中,RGCs可根据其独特的树突结构和突触连接分为约20种形态学亚型(11-19)。小鼠RGCs的整装绘图(图3)展示了哺乳动物RGCs中存在的形态多样性((19)。另见网络视觉神经节细胞章节中人类、猫和兔视网膜的RGCs)。在成年视网膜中,这些RGCs中的大多数在IPL中具有特定的树突分布,如图4所示的小鼠RGCs分支模式示意图。在大多数哺乳动物中,RGCs树突和突触连接的这种层限制分布在出生前和出生后发育期间形成。问题是这种分层是如何产生的。

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