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Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration
Three populations of myogenic cells were isolated from normal mouse skeletal muscle based on their adhesion characteristics and proliferation behaviors. Although two of these populations displayed satellite cell characteristics, a third population of long-time proliferating cells expressing hematopo...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2002
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173424/ https://www.ncbi.nlm.nih.gov/pubmed/12021255 http://dx.doi.org/10.1083/jcb.200108150 |
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author | Qu-Petersen, Zhuqing Deasy, Bridget Jankowski, Ron Ikezawa, Makato Cummins, James Pruchnic, Ryan Mytinger, John Cao, Baohong Gates, Charley Wernig, Anton Huard, Johnny |
author_facet | Qu-Petersen, Zhuqing Deasy, Bridget Jankowski, Ron Ikezawa, Makato Cummins, James Pruchnic, Ryan Mytinger, John Cao, Baohong Gates, Charley Wernig, Anton Huard, Johnny |
author_sort | Qu-Petersen, Zhuqing |
collection | PubMed |
description | Three populations of myogenic cells were isolated from normal mouse skeletal muscle based on their adhesion characteristics and proliferation behaviors. Although two of these populations displayed satellite cell characteristics, a third population of long-time proliferating cells expressing hematopoietic stem cell markers was also identified. This third population comprises cells that retain their phenotype for more than 30 passages with normal karyotype and can differentiate into muscle, neural, and endothelial lineages both in vitro and in vivo. In contrast to the other two populations of myogenic cells, the transplantation of the long-time proliferating cells improved the efficiency of muscle regeneration and dystrophin delivery to dystrophic muscle. The long-time proliferating cells' ability to proliferate in vivo for an extended period of time, combined with their strong capacity for self-renewal, their multipotent differentiation, and their immune-privileged behavior, reveals, at least in part, the basis for the improvement of cell transplantation. Our results suggest that this novel population of muscle-derived stem cells will significantly improve muscle cell–mediated therapies. |
format | Text |
id | pubmed-2173424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21734242008-05-01 Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration Qu-Petersen, Zhuqing Deasy, Bridget Jankowski, Ron Ikezawa, Makato Cummins, James Pruchnic, Ryan Mytinger, John Cao, Baohong Gates, Charley Wernig, Anton Huard, Johnny J Cell Biol Article Three populations of myogenic cells were isolated from normal mouse skeletal muscle based on their adhesion characteristics and proliferation behaviors. Although two of these populations displayed satellite cell characteristics, a third population of long-time proliferating cells expressing hematopoietic stem cell markers was also identified. This third population comprises cells that retain their phenotype for more than 30 passages with normal karyotype and can differentiate into muscle, neural, and endothelial lineages both in vitro and in vivo. In contrast to the other two populations of myogenic cells, the transplantation of the long-time proliferating cells improved the efficiency of muscle regeneration and dystrophin delivery to dystrophic muscle. The long-time proliferating cells' ability to proliferate in vivo for an extended period of time, combined with their strong capacity for self-renewal, their multipotent differentiation, and their immune-privileged behavior, reveals, at least in part, the basis for the improvement of cell transplantation. Our results suggest that this novel population of muscle-derived stem cells will significantly improve muscle cell–mediated therapies. The Rockefeller University Press 2002-05-28 /pmc/articles/PMC2173424/ /pubmed/12021255 http://dx.doi.org/10.1083/jcb.200108150 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Qu-Petersen, Zhuqing Deasy, Bridget Jankowski, Ron Ikezawa, Makato Cummins, James Pruchnic, Ryan Mytinger, John Cao, Baohong Gates, Charley Wernig, Anton Huard, Johnny Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
title | Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
title_full | Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
title_fullStr | Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
title_full_unstemmed | Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
title_short | Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
title_sort | identification of a novel population of muscle stem cells in mice: potential for muscle regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173424/ https://www.ncbi.nlm.nih.gov/pubmed/12021255 http://dx.doi.org/10.1083/jcb.200108150 |
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