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Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle

Fatty and fibrous connective tissue formation is a hallmark of diseased skeletal muscle and deteriorates muscle function. We previously identified non-myogenic mesenchymal progenitors that contribute to adipogenesis and fibrogenesis in mouse skeletal muscle. In this study, we report the identificati...

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Autores principales: Uezumi, A, Fukada, S, Yamamoto, N, Ikemoto-Uezumi, M, Nakatani, M, Morita, M, Yamaguchi, A, Yamada, H, Nishino, I, Hamada, Y, Tsuchida, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001314/
https://www.ncbi.nlm.nih.gov/pubmed/24743741
http://dx.doi.org/10.1038/cddis.2014.161
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author Uezumi, A
Fukada, S
Yamamoto, N
Ikemoto-Uezumi, M
Nakatani, M
Morita, M
Yamaguchi, A
Yamada, H
Nishino, I
Hamada, Y
Tsuchida, K
author_facet Uezumi, A
Fukada, S
Yamamoto, N
Ikemoto-Uezumi, M
Nakatani, M
Morita, M
Yamaguchi, A
Yamada, H
Nishino, I
Hamada, Y
Tsuchida, K
author_sort Uezumi, A
collection PubMed
description Fatty and fibrous connective tissue formation is a hallmark of diseased skeletal muscle and deteriorates muscle function. We previously identified non-myogenic mesenchymal progenitors that contribute to adipogenesis and fibrogenesis in mouse skeletal muscle. In this study, we report the identification and characterization of a human counterpart to these progenitors. By using PDGFRα as a specific marker, mesenchymal progenitors can be identified in the interstitium and isolated from human skeletal muscle. PDGFRα(+) cells represent a cell population distinct from CD56(+) myogenic cells, and adipogenic and fibrogenic potentials were highly enriched in the PDGFRα(+) population. Activation of PDGFRα stimulates proliferation of PDGFRα(+) cells through PI3K-Akt and MEK2-MAPK signaling pathways, and aberrant accumulation of PDGFRα(+) cells was conspicuous in muscles of patients with both genetic and non-genetic muscle diseases. Our results revealed the pathological relevance of PDGFRα(+) mesenchymal progenitors to human muscle diseases and provide a basis for developing therapeutic strategy to treat muscle diseases.
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spelling pubmed-40013142014-04-28 Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle Uezumi, A Fukada, S Yamamoto, N Ikemoto-Uezumi, M Nakatani, M Morita, M Yamaguchi, A Yamada, H Nishino, I Hamada, Y Tsuchida, K Cell Death Dis Original Article Fatty and fibrous connective tissue formation is a hallmark of diseased skeletal muscle and deteriorates muscle function. We previously identified non-myogenic mesenchymal progenitors that contribute to adipogenesis and fibrogenesis in mouse skeletal muscle. In this study, we report the identification and characterization of a human counterpart to these progenitors. By using PDGFRα as a specific marker, mesenchymal progenitors can be identified in the interstitium and isolated from human skeletal muscle. PDGFRα(+) cells represent a cell population distinct from CD56(+) myogenic cells, and adipogenic and fibrogenic potentials were highly enriched in the PDGFRα(+) population. Activation of PDGFRα stimulates proliferation of PDGFRα(+) cells through PI3K-Akt and MEK2-MAPK signaling pathways, and aberrant accumulation of PDGFRα(+) cells was conspicuous in muscles of patients with both genetic and non-genetic muscle diseases. Our results revealed the pathological relevance of PDGFRα(+) mesenchymal progenitors to human muscle diseases and provide a basis for developing therapeutic strategy to treat muscle diseases. Nature Publishing Group 2014-04 2014-04-17 /pmc/articles/PMC4001314/ /pubmed/24743741 http://dx.doi.org/10.1038/cddis.2014.161 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Uezumi, A
Fukada, S
Yamamoto, N
Ikemoto-Uezumi, M
Nakatani, M
Morita, M
Yamaguchi, A
Yamada, H
Nishino, I
Hamada, Y
Tsuchida, K
Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle
title Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle
title_full Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle
title_fullStr Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle
title_full_unstemmed Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle
title_short Identification and characterization of PDGFRα(+) mesenchymal progenitors in human skeletal muscle
title_sort identification and characterization of pdgfrα(+) mesenchymal progenitors in human skeletal muscle
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001314/
https://www.ncbi.nlm.nih.gov/pubmed/24743741
http://dx.doi.org/10.1038/cddis.2014.161
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