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Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus

The spiny mouse, Acomys cahirinus, is an adult mammal capable of remarkable feats of scar-free tissue regeneration after damage to several organs including the skin and the heart. Here we investigate the regenerative properties of the skeletal muscle of A. cahirinus tibialis anterior in comparison t...

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Autores principales: Maden, Malcolm, Brant, Jason Orr, Rubiano, Andres, Sandoval, Aaron Gabriel W., Simmons, Chelsey, Mitchell, Robert, Collin-Hooper, Henry, Jacobson, Jason, Omairi, Saleh, Patel, Ketan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995887/
https://www.ncbi.nlm.nih.gov/pubmed/29892004
http://dx.doi.org/10.1038/s41598-018-27178-7
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author Maden, Malcolm
Brant, Jason Orr
Rubiano, Andres
Sandoval, Aaron Gabriel W.
Simmons, Chelsey
Mitchell, Robert
Collin-Hooper, Henry
Jacobson, Jason
Omairi, Saleh
Patel, Ketan
author_facet Maden, Malcolm
Brant, Jason Orr
Rubiano, Andres
Sandoval, Aaron Gabriel W.
Simmons, Chelsey
Mitchell, Robert
Collin-Hooper, Henry
Jacobson, Jason
Omairi, Saleh
Patel, Ketan
author_sort Maden, Malcolm
collection PubMed
description The spiny mouse, Acomys cahirinus, is an adult mammal capable of remarkable feats of scar-free tissue regeneration after damage to several organs including the skin and the heart. Here we investigate the regenerative properties of the skeletal muscle of A. cahirinus tibialis anterior in comparison to the lab mouse, Mus musculus. The A. cahirinus TA showed a similar distribution of myosin heavy chain fibre types and a reduced proportion of oxidative fibres compared to M. musculus. There were differences in the matrix components of the TA with regard to collagen VI and the biomechanical properties. A. cahirinus TA regenerated faster with a more rapid induction of embryonic myosin and higher levels of dystrophin than in M. musculus fibres. There were lower levels of inflammation (NF-kB), fibrosis (TGFβ-1, collagens) and higher levels of the anti-inflammatory cytokine Cxcl12. There was a difference in macrophage profile between the two species. After multiple rounds of muscle regeneration the M. musculus TA failed to regenerate muscle fibres and instead produced a large numbers of adipocytes whereas the A. cahirinus TA regenerated perfectly. This clearly improved regeneration performance can be explained by differing levels of growth factors such as adiponectin between the two species.
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spelling pubmed-59958872018-06-21 Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus Maden, Malcolm Brant, Jason Orr Rubiano, Andres Sandoval, Aaron Gabriel W. Simmons, Chelsey Mitchell, Robert Collin-Hooper, Henry Jacobson, Jason Omairi, Saleh Patel, Ketan Sci Rep Article The spiny mouse, Acomys cahirinus, is an adult mammal capable of remarkable feats of scar-free tissue regeneration after damage to several organs including the skin and the heart. Here we investigate the regenerative properties of the skeletal muscle of A. cahirinus tibialis anterior in comparison to the lab mouse, Mus musculus. The A. cahirinus TA showed a similar distribution of myosin heavy chain fibre types and a reduced proportion of oxidative fibres compared to M. musculus. There were differences in the matrix components of the TA with regard to collagen VI and the biomechanical properties. A. cahirinus TA regenerated faster with a more rapid induction of embryonic myosin and higher levels of dystrophin than in M. musculus fibres. There were lower levels of inflammation (NF-kB), fibrosis (TGFβ-1, collagens) and higher levels of the anti-inflammatory cytokine Cxcl12. There was a difference in macrophage profile between the two species. After multiple rounds of muscle regeneration the M. musculus TA failed to regenerate muscle fibres and instead produced a large numbers of adipocytes whereas the A. cahirinus TA regenerated perfectly. This clearly improved regeneration performance can be explained by differing levels of growth factors such as adiponectin between the two species. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995887/ /pubmed/29892004 http://dx.doi.org/10.1038/s41598-018-27178-7 Text en © The Author(s) 2018 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
Maden, Malcolm
Brant, Jason Orr
Rubiano, Andres
Sandoval, Aaron Gabriel W.
Simmons, Chelsey
Mitchell, Robert
Collin-Hooper, Henry
Jacobson, Jason
Omairi, Saleh
Patel, Ketan
Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus
title Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus
title_full Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus
title_fullStr Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus
title_full_unstemmed Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus
title_short Perfect chronic skeletal muscle regeneration in adult spiny mice, Acomys cahirinus
title_sort perfect chronic skeletal muscle regeneration in adult spiny mice, acomys cahirinus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995887/
https://www.ncbi.nlm.nih.gov/pubmed/29892004
http://dx.doi.org/10.1038/s41598-018-27178-7
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