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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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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. |
format | Online Article Text |
id | pubmed-4001314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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