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一种在周围神经丛中对靶标选择性轴突再生至关重要的神经胶质细胞依赖性机制。

A glia cell dependent mechanism at a peripheral nerve plexus critical for target-selective axon regeneration.

作者信息

Walker Lauren J, Guevara Camilo, Kawakami Koichi, Granato Michael

机构信息

Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.

Laboratory of Molecular and Developmental Biology, National Institute of Genetics, and Department of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka 411-8540, Japan.

出版信息

bioRxiv. 2023 Jan 5:2023.01.05.522786. doi: 10.1101/2023.01.05.522786.

Abstract

A critical step for functional recovery from peripheral nerve injury is for regenerating axons to connect with their pre-injury targets. Reestablishing pre-injury target specificity is particularly challenging for limb-innervating axons as they encounter a plexus, a network where peripheral nerves converge, axons from different nerves intermingle, and then re-sort into target-specific bundles. Here, we examine this process at a plexus located at the base of the zebrafish pectoral fin, equivalent to tetrapod forelimbs. Using live cell imaging and sparse axon labeling, we find that regenerating motor axons from three nerves coalesce into the plexus. There, they intermingle and sort into distinct branches, and then navigate to their original muscle domains with high fidelity that restores functionality. We demonstrate that this regeneration process includes selective retraction of mistargeted axons, suggesting active correction mechanisms. Moreover, we find that Schwann cells are enriched and associate with axons at the plexus, and that Schwann cell ablation during regeneration causes profound axonal mistargeting. Our data provide the first real time account of regenerating vertebrate motor axons navigating a nerve plexus and reveal a previously unappreciated role for Schwann cells to promote axon sorting at a plexus during regeneration.

摘要

周围神经损伤后功能恢复的关键步骤是再生轴突与损伤前的靶标建立连接。对于支配肢体的轴突而言,重新建立损伤前的靶标特异性尤其具有挑战性,因为它们会遇到一个神经丛,即一个周围神经汇聚、来自不同神经的轴突相互交织,然后重新分类为靶标特异性束状结构的网络。在此,我们在斑马鱼胸鳍基部的一个神经丛处研究这一过程,该神经丛相当于四足动物的前肢。通过活细胞成像和稀疏轴突标记,我们发现来自三条神经的再生运动轴突汇聚到神经丛中。在那里,它们相互交织并分类为不同的分支,然后高保真地导航到其原始肌肉区域并恢复功能。我们证明,这一再生过程包括错误靶向轴突的选择性回缩,提示存在主动校正机制。此外,我们发现施万细胞在神经丛处富集并与轴突相关联,并且再生过程中施万细胞的消融会导致严重的轴突错误靶向。我们的数据首次实时记录了脊椎动物运动轴突在神经丛中的导航过程,并揭示了施万细胞在再生过程中促进神经丛处轴突分类方面此前未被认识到的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ac/9881934/2c50bf751502/nihpp-2023.01.05.522786v1-f0001.jpg

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