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

View ORCID ProfileLauren J Walker, Camilo Guevara, View ORCID ProfileKoichi Kawakami, View ORCID ProfileMichael Granato
doi: https://doi.org/10.1101/2023.01.05.522786
Lauren J Walker
1Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
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  • For correspondence: granatom@pennmedicine.upenn.edu laurenjanewalker@gmail.com
Camilo Guevara
1Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
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Koichi Kawakami
2Laboratory 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
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Michael Granato
1Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
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  • For correspondence: granatom@pennmedicine.upenn.edu laurenjanewalker@gmail.com
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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.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted January 05, 2023.
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A glia cell dependent mechanism at a peripheral nerve plexus critical for target-selective axon regeneration
Lauren J Walker, Camilo Guevara, Koichi Kawakami, Michael Granato
bioRxiv 2023.01.05.522786; doi: https://doi.org/10.1101/2023.01.05.522786
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A glia cell dependent mechanism at a peripheral nerve plexus critical for target-selective axon regeneration
Lauren J Walker, Camilo Guevara, Koichi Kawakami, Michael Granato
bioRxiv 2023.01.05.522786; doi: https://doi.org/10.1101/2023.01.05.522786

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