感光神经节细胞间隙连接网络的结构和功能。

IF 1.1 4区 医学 Q4 NEUROSCIENCES Visual Neuroscience Pub Date : 2021-09-16 DOI:10.1017/S0952523821000134
Xiwu Zhao, Kwoon Y Wong
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引用次数: 1

摘要

内在光敏性视网膜神经节细胞(ipRGCs)不仅可以顺行信号驱动行为反应,还可以逆行信号传递给一些无分泌的中间神经元来调节视网膜生理。我们之前发现,所有具有尖峰性、紧张性兴奋性光反应的移位的无突细胞都接受来自iprgc的间隙连接输入,但iprgc -无突偶联的连接模式和功能作用在很大程度上仍然未知。我们将PoPro1荧光示踪剂注射到6种小鼠ipRGCs中,鉴定偶联的无分泌细胞,并分析后者的形态和电生理特性。我们还研究了基因破坏ipRGC-amacrine偶联如何影响ipRGC光响应。结果表明,iprgc不仅能偶联神经节细胞层的ON-和ON/ off分层无毛细胞,还能偶联神经节细胞层和内核层的off分层无毛细胞。M1型和m3型ipRGC主要与开/关分层的无毛细胞偶联,而其他类型的ipRGC几乎完全与开/关分层的无毛细胞偶联。ipRGCs将基于黑视素的光响应传递给至少93%的偶联无毛细胞。一些on分层iprgc偶联的无毛细胞表现出短暂的超偏振光响应。我们检测到ipRGC和偶联的无腺细胞之间的双向电传输,尽管这种特定细胞对的传输是不对称的,有利于ipRGC-无腺方向。我们还观察到两个与相同ipRGC偶联的无分泌细胞之间的电传输。在这两种耦合情况下,耦合的细胞通常是同步尖峰的。虽然ipRGC-amacrine偶联在一定程度上降低了iprgc基于黑素的内在光响应的峰值发射率,但它使这些响应更加持续和持久。综上所述,iprgc的间隙连接网络涉及更多的非分泌细胞类型,并发挥更多的作用。
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Structure and function of the gap junctional network of photoreceptive ganglion cells.

Intrinsically photosensitive retinal ganglion cells (ipRGCs) signal not only anterogradely to drive behavioral responses, but also retrogradely to some amacrine interneurons to modulate retinal physiology. We previously found that all displaced amacrine cells with spiking, tonic excitatory photoresponses receive gap-junction input from ipRGCs, but the connectivity patterns and functional roles of ipRGC-amacrine coupling remained largely unknown. Here, we injected PoPro1 fluorescent tracer into all six types of mouse ipRGCs to identify coupled amacrine cells, and analyzed the latter's morphological and electrophysiological properties. We also examined how genetically disrupting ipRGC-amacrine coupling affected ipRGC photoresponses. Results showed that ipRGCs couple with not just ON- and ON/OFF-stratified amacrine cells in the ganglion-cell layer as previously reported, but also OFF-stratified amacrine cells in both ganglion-cell and inner nuclear layers. M1- and M3-type ipRGCs couple mainly with ON/OFF-stratified amacrine cells, whereas the other ipRGC types couple almost exclusively with ON-stratified ones. ipRGCs transmit melanopsin-based light responses to at least 93% of the coupled amacrine cells. Some of the ON-stratifying ipRGC-coupled amacrine cells exhibit transient hyperpolarizing light responses. We detected bidirectional electrical transmission between an ipRGC and a coupled amacrine cell, although transmission was asymmetric for this particular cell pair, favoring the ipRGC-to-amacrine direction. We also observed electrical transmission between two amacrine cells coupled to the same ipRGC. In both scenarios of coupling, the coupled cells often spiked synchronously. While ipRGC-amacrine coupling somewhat reduces the peak firing rates of ipRGCs' intrinsic melanopsin-based photoresponses, it renders these responses more sustained and longer-lasting. In summary, ipRGCs' gap junctional network involves more amacrine cell types and plays more roles than previously appreciated.

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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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