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Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype

In the degenerative disease Duchenne muscular dystrophy, inflammatory cells enter muscles in response to repetitive muscle damage. Immune factors are required for muscle regeneration, but chronic inflammation creates a profibrotic milieu that exacerbates disease progression. Osteopontin (OPN) is an...

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Autores principales: Capote, Joana, Kramerova, Irina, Martinez, Leonel, Vetrone, Sylvia, Barton, Elisabeth R., Sweeney, H. Lee, Miceli, M. Carrie, Spencer, Melissa J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084275/
https://www.ncbi.nlm.nih.gov/pubmed/27091452
http://dx.doi.org/10.1083/jcb.201510086
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author Capote, Joana
Kramerova, Irina
Martinez, Leonel
Vetrone, Sylvia
Barton, Elisabeth R.
Sweeney, H. Lee
Miceli, M. Carrie
Spencer, Melissa J.
author_facet Capote, Joana
Kramerova, Irina
Martinez, Leonel
Vetrone, Sylvia
Barton, Elisabeth R.
Sweeney, H. Lee
Miceli, M. Carrie
Spencer, Melissa J.
author_sort Capote, Joana
collection PubMed
description In the degenerative disease Duchenne muscular dystrophy, inflammatory cells enter muscles in response to repetitive muscle damage. Immune factors are required for muscle regeneration, but chronic inflammation creates a profibrotic milieu that exacerbates disease progression. Osteopontin (OPN) is an immunomodulator highly expressed in dystrophic muscles. Ablation of OPN correlates with reduced fibrosis and improved muscle strength as well as reduced natural killer T (NKT) cell counts. Here, we demonstrate that the improved dystrophic phenotype observed with OPN ablation does not result from reductions in NKT cells. OPN ablation skews macrophage polarization toward a pro-regenerative phenotype by reducing M1 and M2a and increasing M2c subsets. These changes are associated with increased expression of pro-regenerative factors insulin-like growth factor 1, leukemia inhibitory factor, and urokinase-type plasminogen activator. Furthermore, altered macrophage polarization correlated with increases in muscle weight and muscle fiber diameter, resulting in long-term improvements in muscle strength and function in mdx mice. These findings suggest that OPN ablation promotes muscle repair via macrophage secretion of pro-myogenic growth factors.
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spelling pubmed-50842752016-10-31 Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype Capote, Joana Kramerova, Irina Martinez, Leonel Vetrone, Sylvia Barton, Elisabeth R. Sweeney, H. Lee Miceli, M. Carrie Spencer, Melissa J. J Cell Biol Research Articles In the degenerative disease Duchenne muscular dystrophy, inflammatory cells enter muscles in response to repetitive muscle damage. Immune factors are required for muscle regeneration, but chronic inflammation creates a profibrotic milieu that exacerbates disease progression. Osteopontin (OPN) is an immunomodulator highly expressed in dystrophic muscles. Ablation of OPN correlates with reduced fibrosis and improved muscle strength as well as reduced natural killer T (NKT) cell counts. Here, we demonstrate that the improved dystrophic phenotype observed with OPN ablation does not result from reductions in NKT cells. OPN ablation skews macrophage polarization toward a pro-regenerative phenotype by reducing M1 and M2a and increasing M2c subsets. These changes are associated with increased expression of pro-regenerative factors insulin-like growth factor 1, leukemia inhibitory factor, and urokinase-type plasminogen activator. Furthermore, altered macrophage polarization correlated with increases in muscle weight and muscle fiber diameter, resulting in long-term improvements in muscle strength and function in mdx mice. These findings suggest that OPN ablation promotes muscle repair via macrophage secretion of pro-myogenic growth factors. The Rockefeller University Press 2016-04-25 /pmc/articles/PMC5084275/ /pubmed/27091452 http://dx.doi.org/10.1083/jcb.201510086 Text en © 2016 Capote et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Capote, Joana
Kramerova, Irina
Martinez, Leonel
Vetrone, Sylvia
Barton, Elisabeth R.
Sweeney, H. Lee
Miceli, M. Carrie
Spencer, Melissa J.
Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
title Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
title_full Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
title_fullStr Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
title_full_unstemmed Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
title_short Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
title_sort osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084275/
https://www.ncbi.nlm.nih.gov/pubmed/27091452
http://dx.doi.org/10.1083/jcb.201510086
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