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Failed reinnervation in aging skeletal muscle
BACKGROUND: Skeletal muscle displays a marked accumulation of denervated myofibers at advanced age, which coincides with an acceleration of muscle atrophy. METHODS: In this study, we evaluated the hypothesis that the accumulation of denervated myofibers in advanced age is due to failed reinnervation...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007704/ https://www.ncbi.nlm.nih.gov/pubmed/27588166 http://dx.doi.org/10.1186/s13395-016-0101-y |
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author | Aare, Sudhakar Spendiff, Sally Vuda, Madhusudanarao Elkrief, Daren Perez, Anna Wu, Qinghua Mayaki, Dominique Hussain, Sabah N. A. Hettwer, Stefan Hepple, Russell T. |
author_facet | Aare, Sudhakar Spendiff, Sally Vuda, Madhusudanarao Elkrief, Daren Perez, Anna Wu, Qinghua Mayaki, Dominique Hussain, Sabah N. A. Hettwer, Stefan Hepple, Russell T. |
author_sort | Aare, Sudhakar |
collection | PubMed |
description | BACKGROUND: Skeletal muscle displays a marked accumulation of denervated myofibers at advanced age, which coincides with an acceleration of muscle atrophy. METHODS: In this study, we evaluated the hypothesis that the accumulation of denervated myofibers in advanced age is due to failed reinnervation by examining muscle from young adult (YA) and very old (VO) rats and from a murine model of sporadic denervation secondary to neurotrypsin over-expression (Sarco mouse). RESULTS: Both aging rat muscle and Sarco mouse muscle exhibited marked fiber-type grouping, consistent with repeating cycles of denervation and reinnervation, yet in VO muscle, rapsyn at the endplate increased and was associated with only a 10 % decline in acetylcholine receptor (AChR) intensity, whereas in Sarco mice, there was a decline in rapsyn and a 25 % decrease in AChR intensity. Transcripts of muscle-specific kinase (21-fold), acetylcholine receptor subunits α (68-fold), ε (threefold) and γ (47-fold), neural cell adhesion molecule (66-fold), and runt-related transcription factor 1 (33-fold) were upregulated in VO muscle of the rat, consistent with the marked persistent denervation evidenced by a large proportion of very small fibers (>20 %). In the Sarco mice, there were much smaller increases in denervation transcripts (0–3.5-fold) and accumulation of very small fibers (2–6 %) compared to the VO rat, suggesting a reduced capacity for reinnervation in aging muscle. Despite the marked persistent denervation in the VO rat muscle, transcripts of neurotrophins involved in promoting axonal sprouting following denervation exhibited no increase, and several miRNAs predicted to suppress neurotrophins were elevated in VO rat. CONCLUSIONS: Our results support the hypothesis that the accumulation of denervated fibers with aging is due to failed reinnervation and that this may be affected by a limited neurotrophin response that mediates axonal sprouting following denervation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13395-016-0101-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5007704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50077042016-09-02 Failed reinnervation in aging skeletal muscle Aare, Sudhakar Spendiff, Sally Vuda, Madhusudanarao Elkrief, Daren Perez, Anna Wu, Qinghua Mayaki, Dominique Hussain, Sabah N. A. Hettwer, Stefan Hepple, Russell T. Skelet Muscle Research BACKGROUND: Skeletal muscle displays a marked accumulation of denervated myofibers at advanced age, which coincides with an acceleration of muscle atrophy. METHODS: In this study, we evaluated the hypothesis that the accumulation of denervated myofibers in advanced age is due to failed reinnervation by examining muscle from young adult (YA) and very old (VO) rats and from a murine model of sporadic denervation secondary to neurotrypsin over-expression (Sarco mouse). RESULTS: Both aging rat muscle and Sarco mouse muscle exhibited marked fiber-type grouping, consistent with repeating cycles of denervation and reinnervation, yet in VO muscle, rapsyn at the endplate increased and was associated with only a 10 % decline in acetylcholine receptor (AChR) intensity, whereas in Sarco mice, there was a decline in rapsyn and a 25 % decrease in AChR intensity. Transcripts of muscle-specific kinase (21-fold), acetylcholine receptor subunits α (68-fold), ε (threefold) and γ (47-fold), neural cell adhesion molecule (66-fold), and runt-related transcription factor 1 (33-fold) were upregulated in VO muscle of the rat, consistent with the marked persistent denervation evidenced by a large proportion of very small fibers (>20 %). In the Sarco mice, there were much smaller increases in denervation transcripts (0–3.5-fold) and accumulation of very small fibers (2–6 %) compared to the VO rat, suggesting a reduced capacity for reinnervation in aging muscle. Despite the marked persistent denervation in the VO rat muscle, transcripts of neurotrophins involved in promoting axonal sprouting following denervation exhibited no increase, and several miRNAs predicted to suppress neurotrophins were elevated in VO rat. CONCLUSIONS: Our results support the hypothesis that the accumulation of denervated fibers with aging is due to failed reinnervation and that this may be affected by a limited neurotrophin response that mediates axonal sprouting following denervation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13395-016-0101-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-01 /pmc/articles/PMC5007704/ /pubmed/27588166 http://dx.doi.org/10.1186/s13395-016-0101-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Aare, Sudhakar Spendiff, Sally Vuda, Madhusudanarao Elkrief, Daren Perez, Anna Wu, Qinghua Mayaki, Dominique Hussain, Sabah N. A. Hettwer, Stefan Hepple, Russell T. Failed reinnervation in aging skeletal muscle |
title | Failed reinnervation in aging skeletal muscle |
title_full | Failed reinnervation in aging skeletal muscle |
title_fullStr | Failed reinnervation in aging skeletal muscle |
title_full_unstemmed | Failed reinnervation in aging skeletal muscle |
title_short | Failed reinnervation in aging skeletal muscle |
title_sort | failed reinnervation in aging skeletal muscle |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007704/ https://www.ncbi.nlm.nih.gov/pubmed/27588166 http://dx.doi.org/10.1186/s13395-016-0101-y |
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