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Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle

BACKGROUND: Klotho is a well-known anti-aging hormone, which serves as a suppressor of aging through a variety of mechanisms. Aging of skeletal muscle is concomitant with a decrease in muscle stem cell function resulting in impaired regeneration. METHODS: Here we investigate the functional role of t...

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Autores principales: Ahrens, Hellen E., Huettemeister, Judith, Schmidt, Manuel, Kaether, Christoph, von Maltzahn, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030782/
https://www.ncbi.nlm.nih.gov/pubmed/29973273
http://dx.doi.org/10.1186/s13395-018-0166-x
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author Ahrens, Hellen E.
Huettemeister, Judith
Schmidt, Manuel
Kaether, Christoph
von Maltzahn, Julia
author_facet Ahrens, Hellen E.
Huettemeister, Judith
Schmidt, Manuel
Kaether, Christoph
von Maltzahn, Julia
author_sort Ahrens, Hellen E.
collection PubMed
description BACKGROUND: Klotho is a well-known anti-aging hormone, which serves as a suppressor of aging through a variety of mechanisms. Aging of skeletal muscle is concomitant with a decrease in muscle stem cell function resulting in impaired regeneration. METHODS: Here we investigate the functional role of the anti-aging hormone Klotho for muscle stem cell function after cardiotoxin-induced injury of skeletal muscle using a klotho hypomorphic mouse line, which is characterized by a premature aging phenotype. Furthermore, we perform floating single myofiber cultures with their adjacent muscle stem cells to investigate the interplay between canonical Wnt signaling and Klotho function. RESULTS: We demonstrate that muscle stem cell numbers are significantly decreased in klotho hypomorphic mice. Furthermore, we show that muscle stem cell function is also severely impaired upon loss of klotho expression, in culture and during regeneration in vivo. Moreover, we demonstrate that addition of recombinant Klotho protein inhibits aberrant excessive Wnt signaling in aged muscle stem cells thereby restoring their functionality. CONCLUSIONS: The anti-aging hormone Klotho counteracts aberrant canonical Wnt signaling in muscle stem cells and might be one of the naturally occurring inhibitors of canonical Wnt signaling in skeletal muscle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13395-018-0166-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60307822018-07-09 Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle Ahrens, Hellen E. Huettemeister, Judith Schmidt, Manuel Kaether, Christoph von Maltzahn, Julia Skelet Muscle Research BACKGROUND: Klotho is a well-known anti-aging hormone, which serves as a suppressor of aging through a variety of mechanisms. Aging of skeletal muscle is concomitant with a decrease in muscle stem cell function resulting in impaired regeneration. METHODS: Here we investigate the functional role of the anti-aging hormone Klotho for muscle stem cell function after cardiotoxin-induced injury of skeletal muscle using a klotho hypomorphic mouse line, which is characterized by a premature aging phenotype. Furthermore, we perform floating single myofiber cultures with their adjacent muscle stem cells to investigate the interplay between canonical Wnt signaling and Klotho function. RESULTS: We demonstrate that muscle stem cell numbers are significantly decreased in klotho hypomorphic mice. Furthermore, we show that muscle stem cell function is also severely impaired upon loss of klotho expression, in culture and during regeneration in vivo. Moreover, we demonstrate that addition of recombinant Klotho protein inhibits aberrant excessive Wnt signaling in aged muscle stem cells thereby restoring their functionality. CONCLUSIONS: The anti-aging hormone Klotho counteracts aberrant canonical Wnt signaling in muscle stem cells and might be one of the naturally occurring inhibitors of canonical Wnt signaling in skeletal muscle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13395-018-0166-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-04 /pmc/articles/PMC6030782/ /pubmed/29973273 http://dx.doi.org/10.1186/s13395-018-0166-x Text en © The Author(s). 2018 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
Ahrens, Hellen E.
Huettemeister, Judith
Schmidt, Manuel
Kaether, Christoph
von Maltzahn, Julia
Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
title Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
title_full Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
title_fullStr Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
title_full_unstemmed Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
title_short Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
title_sort klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030782/
https://www.ncbi.nlm.nih.gov/pubmed/29973273
http://dx.doi.org/10.1186/s13395-018-0166-x
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