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Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model
MicroRNA (miRNA)s are a class of non-coding RNAs that regulate gene expression post-transcriptionally. Muscle-specific miRNA, miRNA (miR)-1, miR-133 and miR-206 play a crucial role in the regulation of muscle development and homeostasis. Muscle injuries are a common muscloskeletal disorder, and the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823166/ https://www.ncbi.nlm.nih.gov/pubmed/19754672 http://dx.doi.org/10.1111/j.1582-4934.2009.00898.x |
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author | Nakasa, Tomoyuki Ishikawa, Masakazu Shi, Ming Shibuya, Hayatoshi Adachi, Nobuo Ochi, Mitsuo |
author_facet | Nakasa, Tomoyuki Ishikawa, Masakazu Shi, Ming Shibuya, Hayatoshi Adachi, Nobuo Ochi, Mitsuo |
author_sort | Nakasa, Tomoyuki |
collection | PubMed |
description | MicroRNA (miRNA)s are a class of non-coding RNAs that regulate gene expression post-transcriptionally. Muscle-specific miRNA, miRNA (miR)-1, miR-133 and miR-206 play a crucial role in the regulation of muscle development and homeostasis. Muscle injuries are a common muscloskeletal disorder, and the most effective treatment has not been established yet. The purpose of this study was to demonstrate that a local injection of double-stranded (ds) miR-1, miR-133 and 206 can accelerate muscle regeneration in a rat skeletal muscle injury model. After the laceration of the rat tibialis anterior muscle, ds miR-1, 133 and 206 mixture mediated atelocollagen was injected into the injured site. The control group was injected with control siRNA. At 1 week after injury, an injection of miRNAs could enhance muscle regeneration morphologically and physiologically, and prevent fibrosis effectively compared to the control siRNA. Administration of exogenous miR-1, 133 and 206 can induce expression of myogenic markers, MyoD1, myogenin and Pax7 in mRNA and expression in the protein level at 3 and 7 days after injury. The combination of miR-1, 133 and 206 can promote myotube differentiation, and the expression of MyoD1, myogenin and Pax7 were up-regulated in C2C12 cells in vitro. Local injection of miR-1, 133 and 206 could be a novel therapeutic strategy in the treatment of skeletal muscle injury. |
format | Online Article Text |
id | pubmed-3823166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38231662015-04-20 Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model Nakasa, Tomoyuki Ishikawa, Masakazu Shi, Ming Shibuya, Hayatoshi Adachi, Nobuo Ochi, Mitsuo J Cell Mol Med Articles MicroRNA (miRNA)s are a class of non-coding RNAs that regulate gene expression post-transcriptionally. Muscle-specific miRNA, miRNA (miR)-1, miR-133 and miR-206 play a crucial role in the regulation of muscle development and homeostasis. Muscle injuries are a common muscloskeletal disorder, and the most effective treatment has not been established yet. The purpose of this study was to demonstrate that a local injection of double-stranded (ds) miR-1, miR-133 and 206 can accelerate muscle regeneration in a rat skeletal muscle injury model. After the laceration of the rat tibialis anterior muscle, ds miR-1, 133 and 206 mixture mediated atelocollagen was injected into the injured site. The control group was injected with control siRNA. At 1 week after injury, an injection of miRNAs could enhance muscle regeneration morphologically and physiologically, and prevent fibrosis effectively compared to the control siRNA. Administration of exogenous miR-1, 133 and 206 can induce expression of myogenic markers, MyoD1, myogenin and Pax7 in mRNA and expression in the protein level at 3 and 7 days after injury. The combination of miR-1, 133 and 206 can promote myotube differentiation, and the expression of MyoD1, myogenin and Pax7 were up-regulated in C2C12 cells in vitro. Local injection of miR-1, 133 and 206 could be a novel therapeutic strategy in the treatment of skeletal muscle injury. Blackwell Publishing Ltd 2010-10 2009-09-14 /pmc/articles/PMC3823166/ /pubmed/19754672 http://dx.doi.org/10.1111/j.1582-4934.2009.00898.x Text en © 2009 The Authors Journal compilation © 2010 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd |
spellingShingle | Articles Nakasa, Tomoyuki Ishikawa, Masakazu Shi, Ming Shibuya, Hayatoshi Adachi, Nobuo Ochi, Mitsuo Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model |
title | Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model |
title_full | Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model |
title_fullStr | Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model |
title_full_unstemmed | Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model |
title_short | Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model |
title_sort | acceleration of muscle regeneration by local injection of muscle-specific micrornas in rat skeletal muscle injury model |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823166/ https://www.ncbi.nlm.nih.gov/pubmed/19754672 http://dx.doi.org/10.1111/j.1582-4934.2009.00898.x |
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