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Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing
Motor unit remodelling involving repeated denervation and re-innervation occurs throughout life. The efficiency of this process declines with age contributing to neuromuscular deficits. This study investigated differentially expressed genes (DEG) in muscle following peroneal nerve crush to model mot...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800362/ https://www.ncbi.nlm.nih.gov/pubmed/35093178 http://dx.doi.org/10.1186/s13395-021-00283-4 |
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author | Staunton, C. A. Owen, E. D. Hemmings, K. Vasilaki, A. McArdle, A. Barrett-Jolley, R. Jackson, M. J. |
author_facet | Staunton, C. A. Owen, E. D. Hemmings, K. Vasilaki, A. McArdle, A. Barrett-Jolley, R. Jackson, M. J. |
author_sort | Staunton, C. A. |
collection | PubMed |
description | Motor unit remodelling involving repeated denervation and re-innervation occurs throughout life. The efficiency of this process declines with age contributing to neuromuscular deficits. This study investigated differentially expressed genes (DEG) in muscle following peroneal nerve crush to model motor unit remodelling in C57BL/6 J mice. Muscle RNA was isolated at 3 days post-crush, RNA libraries were generated using poly-A selection, sequenced and analysed using gene ontology and pathway tools. Three hundred thirty-four DEG were found in quiescent muscle from (26mnth) old compared with (4-6mnth) adult mice and these same DEG were present in muscle from adult mice following nerve crush. Peroneal crush induced 7133 DEG in muscles of adult and 699 DEG in muscles from old mice, although only one DEG (ZCCHC17) was found when directly comparing nerve-crushed muscles from old and adult mice. This analysis revealed key differences in muscle responses which may underlie the diminished ability of old mice to repair following nerve injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13395-021-00283-4. |
format | Online Article Text |
id | pubmed-8800362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88003622022-02-02 Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing Staunton, C. A. Owen, E. D. Hemmings, K. Vasilaki, A. McArdle, A. Barrett-Jolley, R. Jackson, M. J. Skelet Muscle Research Motor unit remodelling involving repeated denervation and re-innervation occurs throughout life. The efficiency of this process declines with age contributing to neuromuscular deficits. This study investigated differentially expressed genes (DEG) in muscle following peroneal nerve crush to model motor unit remodelling in C57BL/6 J mice. Muscle RNA was isolated at 3 days post-crush, RNA libraries were generated using poly-A selection, sequenced and analysed using gene ontology and pathway tools. Three hundred thirty-four DEG were found in quiescent muscle from (26mnth) old compared with (4-6mnth) adult mice and these same DEG were present in muscle from adult mice following nerve crush. Peroneal crush induced 7133 DEG in muscles of adult and 699 DEG in muscles from old mice, although only one DEG (ZCCHC17) was found when directly comparing nerve-crushed muscles from old and adult mice. This analysis revealed key differences in muscle responses which may underlie the diminished ability of old mice to repair following nerve injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13395-021-00283-4. BioMed Central 2022-01-29 /pmc/articles/PMC8800362/ /pubmed/35093178 http://dx.doi.org/10.1186/s13395-021-00283-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Staunton, C. A. Owen, E. D. Hemmings, K. Vasilaki, A. McArdle, A. Barrett-Jolley, R. Jackson, M. J. Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
title | Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
title_full | Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
title_fullStr | Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
title_full_unstemmed | Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
title_short | Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
title_sort | skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800362/ https://www.ncbi.nlm.nih.gov/pubmed/35093178 http://dx.doi.org/10.1186/s13395-021-00283-4 |
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