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miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells
Effect and related mechanisms of miR-101 on the chondrogenic differentiation of rat bone marrow mesenchymal stem cells (MSCs) were investigated. The expression level of miR-101 was detected during chondrogenic differentiation. Three groups were established to study the potential function between miR...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307415/ https://www.ncbi.nlm.nih.gov/pubmed/30651779 http://dx.doi.org/10.3892/etm.2018.6959 |
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author | Gao, Feng Peng, Chuangang Zheng, Changjun Zhang, Shanyong Wu, Minfei |
author_facet | Gao, Feng Peng, Chuangang Zheng, Changjun Zhang, Shanyong Wu, Minfei |
author_sort | Gao, Feng |
collection | PubMed |
description | Effect and related mechanisms of miR-101 on the chondrogenic differentiation of rat bone marrow mesenchymal stem cells (MSCs) were investigated. The expression level of miR-101 was detected during chondrogenic differentiation. Three groups were established to study the potential function between miR-101 and chondrogenic differentiation: miR-NC group (negative control), miR-101 mimics (BMSCs transfected by miR-101 mimics) and mimics + inhibitor (BMSCs transfected by miR-101 mimics and inhibitor), after the induction of chondrogenic differentiation, the cell viability of MSCs and chondrogenic markers were determined, further, the expression level of Sox9 and Runx2 were detected. In our present research, miR-101 was found upregulated during chondrogenic differentiation of MSCs. Compared with the miR-NC group, the cell viability of MSCs was enhanced and the expression level of chondrogenic markers were respectively gained. The expression level of Sox9 was increased but the expression level of Runx2 was decreased by treatment of miR-101 mimics after induction of chondrogenic differentiation. However, these variations of the indicators were reversed by the intervention using the miR-101 inhibitor. Collectively, our research revealed promotion function of miR-101 on chondrogenic differentiation of MSCs, indicating that miR-101 could be a potential therapeutic strategy for the treatment of osteoarthritis (OA). |
format | Online Article Text |
id | pubmed-6307415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-63074152019-01-16 miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells Gao, Feng Peng, Chuangang Zheng, Changjun Zhang, Shanyong Wu, Minfei Exp Ther Med Articles Effect and related mechanisms of miR-101 on the chondrogenic differentiation of rat bone marrow mesenchymal stem cells (MSCs) were investigated. The expression level of miR-101 was detected during chondrogenic differentiation. Three groups were established to study the potential function between miR-101 and chondrogenic differentiation: miR-NC group (negative control), miR-101 mimics (BMSCs transfected by miR-101 mimics) and mimics + inhibitor (BMSCs transfected by miR-101 mimics and inhibitor), after the induction of chondrogenic differentiation, the cell viability of MSCs and chondrogenic markers were determined, further, the expression level of Sox9 and Runx2 were detected. In our present research, miR-101 was found upregulated during chondrogenic differentiation of MSCs. Compared with the miR-NC group, the cell viability of MSCs was enhanced and the expression level of chondrogenic markers were respectively gained. The expression level of Sox9 was increased but the expression level of Runx2 was decreased by treatment of miR-101 mimics after induction of chondrogenic differentiation. However, these variations of the indicators were reversed by the intervention using the miR-101 inhibitor. Collectively, our research revealed promotion function of miR-101 on chondrogenic differentiation of MSCs, indicating that miR-101 could be a potential therapeutic strategy for the treatment of osteoarthritis (OA). D.A. Spandidos 2019-01 2018-11-12 /pmc/articles/PMC6307415/ /pubmed/30651779 http://dx.doi.org/10.3892/etm.2018.6959 Text en Copyright: © Gao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Gao, Feng Peng, Chuangang Zheng, Changjun Zhang, Shanyong Wu, Minfei miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
title | miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
title_full | miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
title_fullStr | miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
title_full_unstemmed | miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
title_short | miRNA-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
title_sort | mirna-101 promotes chondrogenic differentiation in rat bone marrow mesenchymal stem cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307415/ https://www.ncbi.nlm.nih.gov/pubmed/30651779 http://dx.doi.org/10.3892/etm.2018.6959 |
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