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调控排斥性轴突导向的细胞内运输机制。

Intracellular Trafficking Mechanisms that Regulate Repulsive Axon Guidance.

机构信息

Department of Neuroscience, Perelman School of Medicine, University of Pennsylvania, United States.

Department of Neuroscience, Perelman School of Medicine, University of Pennsylvania, United States.

出版信息

Neuroscience. 2023 Jan 1;508:123-136. doi: 10.1016/j.neuroscience.2022.07.012. Epub 2022 Jul 18.

Abstract

Friedrich Bonhoeffer made seminal contributions to the study of axon guidance in the developing nervous system. His discoveries of key cellular and molecular mechanisms that dictate wiring specificity laid the foundation for countless investigators who have followed in his footsteps. Perhaps his most significant contribution was the cloning and characterization of members of the conserved ephrin family of repulsive axon guidance cues. In this review, we highlight the major contributions that Bonhoeffer and his colleagues made to the field of axon guidance, and discuss ongoing investigations into the diverse array of mechanisms that ensure that axon repulsion is precisely regulated to allow for accurate pathfinding. Specifically, we focus our discussion on the post-translational regulation of two major families of repulsive axon guidance factors: ephrin ligands and their Eph receptors, and slit ligands and their Roundabout (Robo) receptors. We will give special emphasis to the ways in which regulated endocytic trafficking events allow navigating axons to adjust their responses to repellant signals and how these trafficking events are intimately related to receptor signaling. By highlighting parallels and differences between the regulation of these two important repulsive axon guidance pathways, we hope to identify key outstanding questions for future investigation.

摘要

弗里德里希·邦霍弗尔(Friedrich Bonhoeffer)在发育神经系统中的轴突导向研究方面做出了开创性的贡献。他发现了决定布线特异性的关键细胞和分子机制,为无数追随他脚步的研究人员奠定了基础。也许他最重要的贡献是克隆和鉴定了保守的 Ephrin 家族排斥性轴突导向线索的成员。在这篇综述中,我们强调了邦霍弗尔及其同事在轴突导向领域的主要贡献,并讨论了正在进行的研究,以了解确保轴突排斥得到精确调节以允许准确寻径的各种机制。具体来说,我们将讨论集中在两种主要的排斥性轴突导向因子的翻译后调节上: Ephrin 配体及其 Eph 受体,以及 slit 配体及其 Roundabout(Robo)受体。我们将特别强调受调节的内吞运输事件如何使导航轴突能够调整其对排斥信号的反应,以及这些运输事件如何与受体信号密切相关。通过突出这两种重要的排斥性轴突导向途径的调节之间的相似之处和差异,我们希望确定未来研究的关键问题。

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