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Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model

Skeletal muscle injury is the most common problem in orthopedic and sports medicine, and severe injury leads to fibrosis and muscle dysfunction. Conventional treatment for successive muscle injury is currently controversial, although new therapies, like cell therapy, seem to be promise. We developed...

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Autores principales: Andrade, Bruno M., Baldanza, Marcelo R., Ribeiro, Karla C., Porto, Anderson, Peçanha, Ramon, Fortes, Fabio S. A., Zapata-Sudo, Gisele, Campos-de-Carvalho, Antonio C., Goldenberg, Regina C. S., Werneck-de-Castro, João Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454438/
https://www.ncbi.nlm.nih.gov/pubmed/26039243
http://dx.doi.org/10.1371/journal.pone.0127561
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author Andrade, Bruno M.
Baldanza, Marcelo R.
Ribeiro, Karla C.
Porto, Anderson
Peçanha, Ramon
Fortes, Fabio S. A.
Zapata-Sudo, Gisele
Campos-de-Carvalho, Antonio C.
Goldenberg, Regina C. S.
Werneck-de-Castro, João Pedro
author_facet Andrade, Bruno M.
Baldanza, Marcelo R.
Ribeiro, Karla C.
Porto, Anderson
Peçanha, Ramon
Fortes, Fabio S. A.
Zapata-Sudo, Gisele
Campos-de-Carvalho, Antonio C.
Goldenberg, Regina C. S.
Werneck-de-Castro, João Pedro
author_sort Andrade, Bruno M.
collection PubMed
description Skeletal muscle injury is the most common problem in orthopedic and sports medicine, and severe injury leads to fibrosis and muscle dysfunction. Conventional treatment for successive muscle injury is currently controversial, although new therapies, like cell therapy, seem to be promise. We developed a model of successive injuries in rat to evaluate the therapeutic potential of bone marrow mesenchymal cells (BMMC) injected directly into the injured muscle. Functional and histological assays were performed 14 and 28 days after the injury protocol by isometric tension recording and picrosirius/Hematoxilin & Eosin staining, respectively. We also evaluated the presence and the fate of BMMC on treated muscles; and muscle fiber regeneration. BMMC treatment increased maximal skeletal muscle contraction 14 and 28 days after muscle injury compared to non-treated group (4.5 ± 1.7 vs 2.5 ± 0.98 N/cm(2), p<0.05 and 8.4 ± 2.3 vs. 5.7 ± 1.3 N/cm(2), p<0.05 respectively). Furthermore, BMMC treatment increased muscle fiber cross-sectional area and the presence of mature muscle fiber 28 days after muscle injury. However, there was no difference in collagen deposition between groups. Immunoassays for cytoskeleton markers of skeletal and smooth muscle cells revealed an apparent integration of the BMMC within the muscle. These data suggest that BMMC transplantation accelerates and improves muscle function recovery in our extensive muscle re-injury model.
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spelling pubmed-44544382015-06-09 Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model Andrade, Bruno M. Baldanza, Marcelo R. Ribeiro, Karla C. Porto, Anderson Peçanha, Ramon Fortes, Fabio S. A. Zapata-Sudo, Gisele Campos-de-Carvalho, Antonio C. Goldenberg, Regina C. S. Werneck-de-Castro, João Pedro PLoS One Research Article Skeletal muscle injury is the most common problem in orthopedic and sports medicine, and severe injury leads to fibrosis and muscle dysfunction. Conventional treatment for successive muscle injury is currently controversial, although new therapies, like cell therapy, seem to be promise. We developed a model of successive injuries in rat to evaluate the therapeutic potential of bone marrow mesenchymal cells (BMMC) injected directly into the injured muscle. Functional and histological assays were performed 14 and 28 days after the injury protocol by isometric tension recording and picrosirius/Hematoxilin & Eosin staining, respectively. We also evaluated the presence and the fate of BMMC on treated muscles; and muscle fiber regeneration. BMMC treatment increased maximal skeletal muscle contraction 14 and 28 days after muscle injury compared to non-treated group (4.5 ± 1.7 vs 2.5 ± 0.98 N/cm(2), p<0.05 and 8.4 ± 2.3 vs. 5.7 ± 1.3 N/cm(2), p<0.05 respectively). Furthermore, BMMC treatment increased muscle fiber cross-sectional area and the presence of mature muscle fiber 28 days after muscle injury. However, there was no difference in collagen deposition between groups. Immunoassays for cytoskeleton markers of skeletal and smooth muscle cells revealed an apparent integration of the BMMC within the muscle. These data suggest that BMMC transplantation accelerates and improves muscle function recovery in our extensive muscle re-injury model. Public Library of Science 2015-06-03 /pmc/articles/PMC4454438/ /pubmed/26039243 http://dx.doi.org/10.1371/journal.pone.0127561 Text en © 2015 Andrade et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Andrade, Bruno M.
Baldanza, Marcelo R.
Ribeiro, Karla C.
Porto, Anderson
Peçanha, Ramon
Fortes, Fabio S. A.
Zapata-Sudo, Gisele
Campos-de-Carvalho, Antonio C.
Goldenberg, Regina C. S.
Werneck-de-Castro, João Pedro
Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model
title Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model
title_full Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model
title_fullStr Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model
title_full_unstemmed Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model
title_short Bone Marrow Mesenchymal Cells Improve Muscle Function in a Skeletal Muscle Re-Injury Model
title_sort bone marrow mesenchymal cells improve muscle function in a skeletal muscle re-injury model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454438/
https://www.ncbi.nlm.nih.gov/pubmed/26039243
http://dx.doi.org/10.1371/journal.pone.0127561
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