Utilizing a culture system for horizontal cells to study neural circuit assembly in the developing mouse retina.

IF 4 3区 医学 Q2 NEUROSCIENCES
Frontiers in Cellular Neuroscience Pub Date : 2026-04-01 eCollection Date: 2026-01-01 DOI:10.3389/fncel.2026.1691122
Ross M Perez, Yong H Park, Ajeet Singh, Collin Todora, Marlon F Mattos, Daniela Becerril, Rajashree Venkatraman, Arlene A Hirano, Nicholas C Brecha, Rinki Ratnapriya, Benjamin J Frankfort, Elizabeth Zuniga-Sanchez
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Abstract

The precise wiring of the nervous system relies on neurons extending their processes at the right time and place to find their appropriate synaptic partner. The mechanisms that determine when and where neurons extend their neurites during synaptogenesis remains a central question in the field. In the present study, we used a cell culture system coupled with live imaging to investigate the wiring mechanisms in the developing mouse retina. We focused on horizontal cells which are a class of interneurons in the outer mouse retina known to synapse selectively to the distinct types of photoreceptors. Previous research has shown horizontal cells extend their neurites and make connections to their respective photoreceptor partner in a temporal- and spatial-dependent manner. However, the mechanisms responsible for their selective wiring to photoreceptors during development remains poorly understood. To answer this question, we developed a horizontal cell culture system to investigate the cellular mechanisms responsible for neurite outgrowth during circuit assembly. Our data shows cultured horizontal cells extend neurites with a similar morphology as in vivo. Moreover, neurite extension of horizontal cells is limited to early developmental stages as young mice extend more complex processes compared to those from adolescent retinas. We also found that horizontal cells, unlike retinal ganglion cells, do not extend neurites when cultured alone and require other retinal neurons to promote neurite outgrowth. In summary, we established a horizontal cell culture system that can be used to decipher the mechanisms involved in neural circuit assembly of the mouse retina.

利用水平细胞培养系统研究发育中的小鼠视网膜中的神经回路组装。
神经系统的精确布线依赖于神经元在正确的时间和地点扩展它们的过程,以找到合适的突触伙伴。在突触发生过程中,决定神经元何时何地延长其神经突的机制仍然是该领域的核心问题。在本研究中,我们使用细胞培养系统结合实时成像来研究发育中的小鼠视网膜的布线机制。我们专注于水平细胞,这是一类中间神经元外小鼠视网膜已知突触选择性地不同类型的光感受器。先前的研究表明,水平细胞扩展其神经突,并以时间和空间依赖的方式与各自的光感受器伙伴建立连接。然而,它们在发育过程中选择连接到光感受器的机制仍然知之甚少。为了回答这个问题,我们开发了一个水平细胞培养系统来研究在电路组装过程中负责神经突生长的细胞机制。我们的数据显示,培养的水平细胞延伸的神经突具有与体内相似的形态。此外,水平细胞的神经突延伸仅限于早期发育阶段,因为与青少年视网膜相比,年轻小鼠的神经突延伸过程更复杂。我们还发现,与视网膜神经节细胞不同,水平细胞在单独培养时不延伸神经突,需要其他视网膜神经元来促进神经突的生长。总之,我们建立了一个水平细胞培养系统,可以用来破译小鼠视网膜神经回路组装的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
3.80%
发文量
627
审稿时长
6-12 weeks
期刊介绍: Frontiers in Cellular Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the cellular mechanisms underlying cell function in the nervous system across all species. Specialty Chief Editors Egidio D‘Angelo at the University of Pavia and Christian Hansel at the University of Chicago are supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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