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Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice
BACKGROUND: Pax7+ satellite cells are required for skeletal muscle fiber growth during post-natal development in mice. Satellite cell-mediated myonuclear accretion also appears to persist into early adulthood. Given the important role of satellite cells during muscle development, we hypothesized tha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504676/ https://www.ncbi.nlm.nih.gov/pubmed/28693603 http://dx.doi.org/10.1186/s13395-017-0132-z |
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author | Murach, Kevin A. White, Sarah H. Wen, Yuan Ho, Angel Dupont-Versteegden, Esther E. McCarthy, John J. Peterson, Charlotte A. |
author_facet | Murach, Kevin A. White, Sarah H. Wen, Yuan Ho, Angel Dupont-Versteegden, Esther E. McCarthy, John J. Peterson, Charlotte A. |
author_sort | Murach, Kevin A. |
collection | PubMed |
description | BACKGROUND: Pax7+ satellite cells are required for skeletal muscle fiber growth during post-natal development in mice. Satellite cell-mediated myonuclear accretion also appears to persist into early adulthood. Given the important role of satellite cells during muscle development, we hypothesized that the necessity of satellite cells for adaptation to an imposed hypertrophic stimulus depends on maturational age. METHODS: Pax7(CreER)-R26R(DTA) mice were treated for 5 days with vehicle (satellite cell-replete, SC+) or tamoxifen (satellite cell-depleted, SC-) at 2 months (young) and 4 months (mature) of age. Following a 2-week washout, mice were subjected to sham surgery or 10 day synergist ablation overload of the plantaris (n = 6–9 per group). The surgical approach minimized regeneration, de novo fiber formation, and fiber splitting while promoting muscle fiber growth. Satellite cell density (Pax7+ cells/fiber), embryonic myosin heavy chain expression (eMyHC), and muscle fiber cross sectional area (CSA) were evaluated via immunohistochemistry. Myonuclei (myonuclei/100 mm) were counted on isolated single muscle fibers. RESULTS: Tamoxifen treatment depleted satellite cells by ≥90% and prevented myonuclear accretion with overload in young and mature mice (p < 0.05). Satellite cells did not recover in SC- mice after overload. Average muscle fiber CSA increased ~20% in young SC+ (p = 0.07), mature SC+ (p < 0.05), and mature SC- mice (p < 0.05). In contrast, muscle fiber hypertrophy was prevented in young SC- mice. Muscle fiber number increased only in mature mice after overload (p < 0.05), and eMyHC expression was variable, specifically in mature SC+ mice. CONCLUSIONS: Reliance on satellite cells for overload-induced hypertrophy is dependent on maturational age, and global responses to overload differ in young versus mature mice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13395-017-0132-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5504676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55046762017-07-12 Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice Murach, Kevin A. White, Sarah H. Wen, Yuan Ho, Angel Dupont-Versteegden, Esther E. McCarthy, John J. Peterson, Charlotte A. Skelet Muscle Research BACKGROUND: Pax7+ satellite cells are required for skeletal muscle fiber growth during post-natal development in mice. Satellite cell-mediated myonuclear accretion also appears to persist into early adulthood. Given the important role of satellite cells during muscle development, we hypothesized that the necessity of satellite cells for adaptation to an imposed hypertrophic stimulus depends on maturational age. METHODS: Pax7(CreER)-R26R(DTA) mice were treated for 5 days with vehicle (satellite cell-replete, SC+) or tamoxifen (satellite cell-depleted, SC-) at 2 months (young) and 4 months (mature) of age. Following a 2-week washout, mice were subjected to sham surgery or 10 day synergist ablation overload of the plantaris (n = 6–9 per group). The surgical approach minimized regeneration, de novo fiber formation, and fiber splitting while promoting muscle fiber growth. Satellite cell density (Pax7+ cells/fiber), embryonic myosin heavy chain expression (eMyHC), and muscle fiber cross sectional area (CSA) were evaluated via immunohistochemistry. Myonuclei (myonuclei/100 mm) were counted on isolated single muscle fibers. RESULTS: Tamoxifen treatment depleted satellite cells by ≥90% and prevented myonuclear accretion with overload in young and mature mice (p < 0.05). Satellite cells did not recover in SC- mice after overload. Average muscle fiber CSA increased ~20% in young SC+ (p = 0.07), mature SC+ (p < 0.05), and mature SC- mice (p < 0.05). In contrast, muscle fiber hypertrophy was prevented in young SC- mice. Muscle fiber number increased only in mature mice after overload (p < 0.05), and eMyHC expression was variable, specifically in mature SC+ mice. CONCLUSIONS: Reliance on satellite cells for overload-induced hypertrophy is dependent on maturational age, and global responses to overload differ in young versus mature mice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13395-017-0132-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-10 /pmc/articles/PMC5504676/ /pubmed/28693603 http://dx.doi.org/10.1186/s13395-017-0132-z Text en © The Author(s). 2017 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 Murach, Kevin A. White, Sarah H. Wen, Yuan Ho, Angel Dupont-Versteegden, Esther E. McCarthy, John J. Peterson, Charlotte A. Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
title | Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
title_full | Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
title_fullStr | Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
title_full_unstemmed | Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
title_short | Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
title_sort | differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504676/ https://www.ncbi.nlm.nih.gov/pubmed/28693603 http://dx.doi.org/10.1186/s13395-017-0132-z |
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