Signaling - transcription interactions in mouse retinal ganglion cells early axon pathfinding -a literature review.

4区 医学 Q4 Medicine
Diabetologe Pub Date : 2023-05-17 eCollection Date: 2023-01-01 DOI:10.3389/fopht.2023.1180142
Raluca Paşcalău, Tudor Constantin Badea
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引用次数: 0

Abstract

Sending an axon out of the eye and into the target brain nuclei is the defining feature of retinal ganglion cells (RGCs). The literature on RGC axon pathfinding is vast, but it focuses mostly on decision making events such as midline crossing at the optic chiasm or retinotopic mapping at the target nuclei. In comparison, the exit of RGC axons out of the eye is much less explored. The first checkpoint on the RGC axons' path is the optic cup - optic stalk junction (OC-OS). OC-OS development and the exit of the RGC pioneer axons out of the eye are coordinated spatially and temporally. By the time the optic nerve head domain is specified, the optic fissure margins are in contact and the fusion process is ongoing, the first RGCs are born in its proximity and send pioneer axons in the optic stalk. RGC differentiation continues in centrifugal waves. Later born RGC axons fasciculate with the more mature axons. Growth cones at the end of the axons respond to guidance cues to adopt a centripetal direction, maintain nerve fiber layer restriction and to leave the optic cup. Although there is extensive information on OC-OS development, we still have important unanswered questions regarding its contribution to the exit of the RGC axons out of the eye. We are still to distinguish the morphogens of the OC-OS from the axon guidance molecules which are expressed in the same place at the same time. The early RGC transcription programs responsible for axon emergence and pathfinding are also unknown. This review summarizes the molecular mechanisms for early RGC axon guidance by contextualizing mouse knock-out studies on OC-OS development with the recent transcriptomic studies on developing RGCs in an attempt to contribute to the understanding of human optic nerve developmental anomalies. The published data summarized here suggests that the developing optic nerve head provides a physical channel (the closing optic fissure) as well as molecular guidance cues for the pioneer RGC axons to exit the eye.

小鼠视网膜神经节细胞早期轴突寻路中的信号-转录相互作用--文献综述。
将轴突送出眼球并送入大脑靶核是视网膜神经节细胞(RGC)的显著特征。有关RGC轴突寻路的文献浩如烟海,但主要集中于决策事件,如在视交叉的中线交叉或在靶核的视网膜异位映射。相比之下,关于 RGC 轴突离开眼球的探索要少得多。RGC轴突路径上的第一个检查点是视杯-视柄交界处(OC-OS)。OC-OS的发育和RGC先驱轴突离开眼球在空间和时间上是相互协调的。当视神经头域确定、视神经裂隙边缘接触以及融合过程正在进行时,第一批RGC在其附近诞生,并将先驱轴突送入视柄。RGC 的分化以离心波的形式继续进行。较晚出生的 RGC 轴突会与较成熟的轴突形成束状。轴突末端的生长锥对引导线索做出反应,采用向心方向,保持神经纤维层限制并离开视杯。尽管我们已经掌握了大量有关OC-OS发育的信息,但关于它对RGC轴突离开眼球所起的作用,我们仍有一些重要的未解之谜。我们仍需将OC-OS的形态发生因子与轴突导向分子区分开来,因为轴突导向分子是在同一时间同一地点表达的。负责轴突出现和寻路的早期RGC转录程序也尚不清楚。本综述总结了早期RGC轴突导向的分子机制,将小鼠OC-OS发育的基因敲除研究与最近关于发育中RGC的转录组学研究结合起来,试图为理解人类视神经发育异常做出贡献。本文总结的已发表数据表明,发育中的视神经头为先驱RGC轴突离开眼球提供了物理通道(闭合视裂)和分子引导线索。
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
Diabetologe
Diabetologe ENDOCRINOLOGY & METABOLISM-
CiteScore
0.40
自引率
0.00%
发文量
53
审稿时长
6-12 weeks
期刊介绍: Der Diabetologe offers up-to-date information for all diabetologists working in practical and clinical environments and scientists who are particularly interested in issues of diabetology. The focus is on current developments regarding prevention, diagnostic approaches, management of complications and current therapy strategies. Comprehensive reviews on a specific topical issue provide evidenced based information on diagnostics and therapy. Review articles under the rubric ''Continuing Medical Education'' present verified results of scientific research and their integration into daily practice.
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