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Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice

Schwann cells (SCs) are integral to the formation and function of the peripheral nervous system (PNS). Exemplifying their importance, the loss or dysfunction of SCs is a feature of a myriad of diseases and conditions that compromise the PNS. Thus, it remains essential to understand the rules that go...

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Autores principales: Hastings, Robert Louis, Mikesh, Michelle, Lee, Young il, Thompson, Wesley J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341867/
https://www.ncbi.nlm.nih.gov/pubmed/32636481
http://dx.doi.org/10.1038/s41598-020-67630-1
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author Hastings, Robert Louis
Mikesh, Michelle
Lee, Young il
Thompson, Wesley J.
author_facet Hastings, Robert Louis
Mikesh, Michelle
Lee, Young il
Thompson, Wesley J.
author_sort Hastings, Robert Louis
collection PubMed
description Schwann cells (SCs) are integral to the formation and function of the peripheral nervous system (PNS). Exemplifying their importance, the loss or dysfunction of SCs is a feature of a myriad of diseases and conditions that compromise the PNS. Thus, it remains essential to understand the rules that govern the proliferation, differentiation and reconnection of Schwann cells with peripheral axons. Here, we examined the consequences of locally and acutely ablating terminal Schwann cells (tSCs) at the adult mouse neuromuscular junction (NMJ) by using mice expressing diphtheria toxin receptor (DTR) preferentially in tSCs compared to myelinating SCs followed by local application of diphtheria toxin (DTX). After DTX application, tSCs died but, importantly and contrary to expectations, their associated motor axons did not fully degenerate. Within 3 weeks, tSCs returned and reestablished coverage of the synapse with increased numbers. Furthermore, the post-synaptic muscle fibers displayed increased distinct clusters of acetylcholine receptors and axon terminals exhibited numerous terminal varicosities. The lack of degeneration of bare motor axon terminals and the morphological remodeling that occurs upon the return of tSCs to the NMJ may have wider implications for the mechanisms governing tSC occupancy of the adult NMJ and for conditions that adversely affect tSCs.
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spelling pubmed-73418672020-07-09 Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice Hastings, Robert Louis Mikesh, Michelle Lee, Young il Thompson, Wesley J. Sci Rep Article Schwann cells (SCs) are integral to the formation and function of the peripheral nervous system (PNS). Exemplifying their importance, the loss or dysfunction of SCs is a feature of a myriad of diseases and conditions that compromise the PNS. Thus, it remains essential to understand the rules that govern the proliferation, differentiation and reconnection of Schwann cells with peripheral axons. Here, we examined the consequences of locally and acutely ablating terminal Schwann cells (tSCs) at the adult mouse neuromuscular junction (NMJ) by using mice expressing diphtheria toxin receptor (DTR) preferentially in tSCs compared to myelinating SCs followed by local application of diphtheria toxin (DTX). After DTX application, tSCs died but, importantly and contrary to expectations, their associated motor axons did not fully degenerate. Within 3 weeks, tSCs returned and reestablished coverage of the synapse with increased numbers. Furthermore, the post-synaptic muscle fibers displayed increased distinct clusters of acetylcholine receptors and axon terminals exhibited numerous terminal varicosities. The lack of degeneration of bare motor axon terminals and the morphological remodeling that occurs upon the return of tSCs to the NMJ may have wider implications for the mechanisms governing tSC occupancy of the adult NMJ and for conditions that adversely affect tSCs. Nature Publishing Group UK 2020-07-07 /pmc/articles/PMC7341867/ /pubmed/32636481 http://dx.doi.org/10.1038/s41598-020-67630-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hastings, Robert Louis
Mikesh, Michelle
Lee, Young il
Thompson, Wesley J.
Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice
title Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice
title_full Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice
title_fullStr Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice
title_full_unstemmed Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice
title_short Morphological remodeling during recovery of the neuromuscular junction from terminal Schwann cell ablation in adult mice
title_sort morphological remodeling during recovery of the neuromuscular junction from terminal schwann cell ablation in adult mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341867/
https://www.ncbi.nlm.nih.gov/pubmed/32636481
http://dx.doi.org/10.1038/s41598-020-67630-1
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