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miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells

Bone morphogenetic proteins (BMPs), particularly BMP9, have been shown to promote the osteogenic differentiation of murine multilineage cells (MMCs) and to promote bone formation in bone diseases; however, the mechanisms involved remain poorly understood. MicroRNAs (miRNAs or miRs) have been proven...

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Autores principales: SONG, QILING, ZHONG, LIANG, CHEN, CHU, TANG, ZUCHUAN, LIU, HONGXIA, ZHOU, YIQIN, TANG, MIN, ZHOU, LAN, ZUO, GUOWEI, LUO, JINYONG, ZHANG, YAN, SHI, QIONG, WENG, YAGUANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678163/
https://www.ncbi.nlm.nih.gov/pubmed/26460584
http://dx.doi.org/10.3892/ijmm.2015.2363
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author SONG, QILING
ZHONG, LIANG
CHEN, CHU
TANG, ZUCHUAN
LIU, HONGXIA
ZHOU, YIQIN
TANG, MIN
ZHOU, LAN
ZUO, GUOWEI
LUO, JINYONG
ZHANG, YAN
SHI, QIONG
WENG, YAGUANG
author_facet SONG, QILING
ZHONG, LIANG
CHEN, CHU
TANG, ZUCHUAN
LIU, HONGXIA
ZHOU, YIQIN
TANG, MIN
ZHOU, LAN
ZUO, GUOWEI
LUO, JINYONG
ZHANG, YAN
SHI, QIONG
WENG, YAGUANG
author_sort SONG, QILING
collection PubMed
description Bone morphogenetic proteins (BMPs), particularly BMP9, have been shown to promote the osteogenic differentiation of murine multilineage cells (MMCs) and to promote bone formation in bone diseases; however, the mechanisms involved remain poorly understood. MicroRNAs (miRNAs or miRs) have been proven to regulate mesenchymal stem cell (MSC) differentiation. In this study, we identified a novel mechanism that unravels the functional axis of a key miRNA (miR-21) which contributes to BMP9-induced osteogenic differentiation. We screened differentially expressed miRNAs in MMCs during BMP9-induced osteogenic differentiation and found that miR-21 was significantly upregulated by BMP9 during the osteogenesis of MMCs. Furthermore, miR-21 was confirmed to promote the osteogenic differentiation of the MMCs by suppressing Smad7, which negatively regulates the osteogenic differentiation of MMCs. The upregulation of miR-21 may promote the osteogenic differentiation of MMCs in synergy with BMP9. The findings of our study revealed a novel function of miR-21, and suggest that the overexpression of miR-21 contributes to bone formation by promoting BMP9-induced osteogenic differentiation. Our data may provide a molecular basis for the development of novel therapeutic strategies to treat bone diseases, such as osteoporosis and other inflammatory bone diseases.
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spelling pubmed-46781632015-12-21 miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells SONG, QILING ZHONG, LIANG CHEN, CHU TANG, ZUCHUAN LIU, HONGXIA ZHOU, YIQIN TANG, MIN ZHOU, LAN ZUO, GUOWEI LUO, JINYONG ZHANG, YAN SHI, QIONG WENG, YAGUANG Int J Mol Med Articles Bone morphogenetic proteins (BMPs), particularly BMP9, have been shown to promote the osteogenic differentiation of murine multilineage cells (MMCs) and to promote bone formation in bone diseases; however, the mechanisms involved remain poorly understood. MicroRNAs (miRNAs or miRs) have been proven to regulate mesenchymal stem cell (MSC) differentiation. In this study, we identified a novel mechanism that unravels the functional axis of a key miRNA (miR-21) which contributes to BMP9-induced osteogenic differentiation. We screened differentially expressed miRNAs in MMCs during BMP9-induced osteogenic differentiation and found that miR-21 was significantly upregulated by BMP9 during the osteogenesis of MMCs. Furthermore, miR-21 was confirmed to promote the osteogenic differentiation of the MMCs by suppressing Smad7, which negatively regulates the osteogenic differentiation of MMCs. The upregulation of miR-21 may promote the osteogenic differentiation of MMCs in synergy with BMP9. The findings of our study revealed a novel function of miR-21, and suggest that the overexpression of miR-21 contributes to bone formation by promoting BMP9-induced osteogenic differentiation. Our data may provide a molecular basis for the development of novel therapeutic strategies to treat bone diseases, such as osteoporosis and other inflammatory bone diseases. D.A. Spandidos 2015-12 2015-10-09 /pmc/articles/PMC4678163/ /pubmed/26460584 http://dx.doi.org/10.3892/ijmm.2015.2363 Text en Copyright: © Song 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
SONG, QILING
ZHONG, LIANG
CHEN, CHU
TANG, ZUCHUAN
LIU, HONGXIA
ZHOU, YIQIN
TANG, MIN
ZHOU, LAN
ZUO, GUOWEI
LUO, JINYONG
ZHANG, YAN
SHI, QIONG
WENG, YAGUANG
miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
title miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
title_full miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
title_fullStr miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
title_full_unstemmed miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
title_short miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
title_sort mir-21 synergizes with bmp9 in osteogenic differentiation by activating the bmp9/smad signaling pathway in murine multilineage cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678163/
https://www.ncbi.nlm.nih.gov/pubmed/26460584
http://dx.doi.org/10.3892/ijmm.2015.2363
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