Cargando…
Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse
The coordinated movement of many organisms relies on efficient nerve–muscle communication at the neuromuscular junction (NMJ), a peripheral synapse composed of a presynaptic motor axon terminal, a postsynaptic muscle specialization, and non‐myelinating terminal Schwann cells. NMJ dysfunctions are ca...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986695/ https://www.ncbi.nlm.nih.gov/pubmed/33336525 http://dx.doi.org/10.1111/brv.12675 |
_version_ | 1783668492912820224 |
---|---|
author | Zelada, Diego Bermedo‐García, Francisca Collao, Nicolás Henríquez, Juan P. |
author_facet | Zelada, Diego Bermedo‐García, Francisca Collao, Nicolás Henríquez, Juan P. |
author_sort | Zelada, Diego |
collection | PubMed |
description | The coordinated movement of many organisms relies on efficient nerve–muscle communication at the neuromuscular junction (NMJ), a peripheral synapse composed of a presynaptic motor axon terminal, a postsynaptic muscle specialization, and non‐myelinating terminal Schwann cells. NMJ dysfunctions are caused by traumatic spinal cord or peripheral nerve injuries as well as by severe motor pathologies. Compared to the central nervous system, the peripheral nervous system displays remarkable regenerating abilities; however, this capacity is limited by the denervation time frame and depends on the establishment of permissive regenerative niches. At the injury site, detailed information is available regarding the cells, molecules, and mechanisms involved in nerve regeneration and repair. However, a regenerative niche at the final functional step of peripheral motor innervation, i.e. at the mature neuromuscular synapse, has not been deciphered. In this review, we integrate classic and recent evidence describing the cells and molecules that could orchestrate a dynamic ecosystem to accomplish successful NMJ regeneration. We propose that such a regenerative niche must ensure at least two fundamental steps for successful NMJ regeneration: the proper arrival of incoming regenerating axons to denervated postsynaptic muscle domains, and the resilience of those postsynaptic domains, in morphological and functional terms. We here describe and combine the main cellular and molecular responses involved in each of these steps as potential targets to help successful NMJ regeneration. |
format | Online Article Text |
id | pubmed-7986695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-79866952021-03-25 Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse Zelada, Diego Bermedo‐García, Francisca Collao, Nicolás Henríquez, Juan P. Biol Rev Camb Philos Soc Original Articles The coordinated movement of many organisms relies on efficient nerve–muscle communication at the neuromuscular junction (NMJ), a peripheral synapse composed of a presynaptic motor axon terminal, a postsynaptic muscle specialization, and non‐myelinating terminal Schwann cells. NMJ dysfunctions are caused by traumatic spinal cord or peripheral nerve injuries as well as by severe motor pathologies. Compared to the central nervous system, the peripheral nervous system displays remarkable regenerating abilities; however, this capacity is limited by the denervation time frame and depends on the establishment of permissive regenerative niches. At the injury site, detailed information is available regarding the cells, molecules, and mechanisms involved in nerve regeneration and repair. However, a regenerative niche at the final functional step of peripheral motor innervation, i.e. at the mature neuromuscular synapse, has not been deciphered. In this review, we integrate classic and recent evidence describing the cells and molecules that could orchestrate a dynamic ecosystem to accomplish successful NMJ regeneration. We propose that such a regenerative niche must ensure at least two fundamental steps for successful NMJ regeneration: the proper arrival of incoming regenerating axons to denervated postsynaptic muscle domains, and the resilience of those postsynaptic domains, in morphological and functional terms. We here describe and combine the main cellular and molecular responses involved in each of these steps as potential targets to help successful NMJ regeneration. Blackwell Publishing Ltd 2020-12-17 2021-04 /pmc/articles/PMC7986695/ /pubmed/33336525 http://dx.doi.org/10.1111/brv.12675 Text en © 2020 The Authors. Biological Reviews published by John Wiley & Sons Ltd on behalf of Cambridge Philosophical Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Zelada, Diego Bermedo‐García, Francisca Collao, Nicolás Henríquez, Juan P. Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
title | Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
title_full | Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
title_fullStr | Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
title_full_unstemmed | Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
title_short | Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
title_sort | motor function recovery: deciphering a regenerative niche at the neuromuscular synapse |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986695/ https://www.ncbi.nlm.nih.gov/pubmed/33336525 http://dx.doi.org/10.1111/brv.12675 |
work_keys_str_mv | AT zeladadiego motorfunctionrecoverydecipheringaregenerativenicheattheneuromuscularsynapse AT bermedogarciafrancisca motorfunctionrecoverydecipheringaregenerativenicheattheneuromuscularsynapse AT collaonicolas motorfunctionrecoverydecipheringaregenerativenicheattheneuromuscularsynapse AT henriquezjuanp motorfunctionrecoverydecipheringaregenerativenicheattheneuromuscularsynapse |