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The body region specificity in murine models of muscle regeneration and atrophy
AIM: Skeletal muscles are distributed throughout the body, presenting a variety of sizes, shapes and functions. Here, we examined whether muscle regeneration and atrophy occurred homogeneously throughout the body in mouse models. METHODS: Acute muscle regeneration was induced by a single intramuscul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757168/ https://www.ncbi.nlm.nih.gov/pubmed/32875719 http://dx.doi.org/10.1111/apha.13553 |
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author | Yoshioka, Kiyoshi Kitajima, Yasuo Seko, Daiki Tsuchiya, Yoshifumi Ono, Yusuke |
author_facet | Yoshioka, Kiyoshi Kitajima, Yasuo Seko, Daiki Tsuchiya, Yoshifumi Ono, Yusuke |
author_sort | Yoshioka, Kiyoshi |
collection | PubMed |
description | AIM: Skeletal muscles are distributed throughout the body, presenting a variety of sizes, shapes and functions. Here, we examined whether muscle regeneration and atrophy occurred homogeneously throughout the body in mouse models. METHODS: Acute muscle regeneration was induced by a single intramuscular injection of cardiotoxin in adult mice. Chronic muscle regeneration was assessed in mdx mice. Muscle atrophy in different muscles was evaluated by cancer cachexia, ageing and castration mouse models. RESULTS: We found that, in the cardiotoxin‐injected acute muscle injury model, head muscles slowly regenerated, while limb muscles exhibited a rapid regeneration and even overgrowth. This overgrowth was also observed in limb muscles alone (but not in head muscles) in mdx mice as chronic injury models. We described the body region–specific decline in the muscle mass in muscle atrophy models: cancer cachexia‐induced, aged and castrated mice. The positional identities, including gene expression profiles and hormone sensitivity, were robustly preserved in the ectopically engrafted satellite cell‐derived muscles in the castrated model. CONCLUSION: Our results indicate that positional identities in muscles should be considered for the development of efficient regenerative therapies for muscle weakness, such as muscular dystrophy and age‐related sarcopenia. |
format | Online Article Text |
id | pubmed-7757168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77571682020-12-28 The body region specificity in murine models of muscle regeneration and atrophy Yoshioka, Kiyoshi Kitajima, Yasuo Seko, Daiki Tsuchiya, Yoshifumi Ono, Yusuke Acta Physiol (Oxf) Muscle Physiology AIM: Skeletal muscles are distributed throughout the body, presenting a variety of sizes, shapes and functions. Here, we examined whether muscle regeneration and atrophy occurred homogeneously throughout the body in mouse models. METHODS: Acute muscle regeneration was induced by a single intramuscular injection of cardiotoxin in adult mice. Chronic muscle regeneration was assessed in mdx mice. Muscle atrophy in different muscles was evaluated by cancer cachexia, ageing and castration mouse models. RESULTS: We found that, in the cardiotoxin‐injected acute muscle injury model, head muscles slowly regenerated, while limb muscles exhibited a rapid regeneration and even overgrowth. This overgrowth was also observed in limb muscles alone (but not in head muscles) in mdx mice as chronic injury models. We described the body region–specific decline in the muscle mass in muscle atrophy models: cancer cachexia‐induced, aged and castrated mice. The positional identities, including gene expression profiles and hormone sensitivity, were robustly preserved in the ectopically engrafted satellite cell‐derived muscles in the castrated model. CONCLUSION: Our results indicate that positional identities in muscles should be considered for the development of efficient regenerative therapies for muscle weakness, such as muscular dystrophy and age‐related sarcopenia. John Wiley and Sons Inc. 2020-09-17 2021-01 /pmc/articles/PMC7757168/ /pubmed/32875719 http://dx.doi.org/10.1111/apha.13553 Text en © 2020 The Authors. Acta Physiologica published by John Wiley & Sons Ltd on behalf of Scandinavian Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Muscle Physiology Yoshioka, Kiyoshi Kitajima, Yasuo Seko, Daiki Tsuchiya, Yoshifumi Ono, Yusuke The body region specificity in murine models of muscle regeneration and atrophy |
title | The body region specificity in murine models of muscle regeneration and atrophy |
title_full | The body region specificity in murine models of muscle regeneration and atrophy |
title_fullStr | The body region specificity in murine models of muscle regeneration and atrophy |
title_full_unstemmed | The body region specificity in murine models of muscle regeneration and atrophy |
title_short | The body region specificity in murine models of muscle regeneration and atrophy |
title_sort | body region specificity in murine models of muscle regeneration and atrophy |
topic | Muscle Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757168/ https://www.ncbi.nlm.nih.gov/pubmed/32875719 http://dx.doi.org/10.1111/apha.13553 |
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