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miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs

We recently reported that maxillary sinus membrane stem cells (MSMSCs) have osteogenic potential. However, the biological mechanisms of bone formation remain unclear. In this study, we investigated the role and mechanisms of microRNAs (miRNAs) in the osteogenic differentiation of MSMSCs. The express...

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Autores principales: Zhu, ShuangXi, Peng, Wei, Li, Xiang, Weng, JunQuan, Zhang, Xing, Guo, JunBing, Huang, DaiYing, Rong, Qiong, Chen, SongLing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384002/
https://www.ncbi.nlm.nih.gov/pubmed/28387248
http://dx.doi.org/10.1038/srep46136
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author Zhu, ShuangXi
Peng, Wei
Li, Xiang
Weng, JunQuan
Zhang, Xing
Guo, JunBing
Huang, DaiYing
Rong, Qiong
Chen, SongLing
author_facet Zhu, ShuangXi
Peng, Wei
Li, Xiang
Weng, JunQuan
Zhang, Xing
Guo, JunBing
Huang, DaiYing
Rong, Qiong
Chen, SongLing
author_sort Zhu, ShuangXi
collection PubMed
description We recently reported that maxillary sinus membrane stem cells (MSMSCs) have osteogenic potential. However, the biological mechanisms of bone formation remain unclear. In this study, we investigated the role and mechanisms of microRNAs (miRNAs) in the osteogenic differentiation of MSMSCs. The expression of miRNAs was determined in differentiated MSMSCs by comprehensive miRNA microarray analysis and quantitative RT-PCR (qRT-PCR). We selected miR-1827 for functional follow-up studies to explore its significance in MSMSCs. Here, miR-1827 was found to be up-regulated during osteogenic differentiation of MSMSCs. Over expression of miR-1827 inhibited osteogenic differentiation of MSMSCs in vitro, whereas the repression of miR-1827 greatly promoted cell differentiation. Further experiments confirmed that insulin-like growth factor 1 (IGF1) is a direct target of miR-1827. miR-1827 inhibited osteogenic differentiation partially via IGF1, which in turn is a positive regulator of osteogenic differentiation. Moreover, miR-1827 suppressed ectopic bone formation and silencing of miR-1827 led to increased bone formation in vivo. In summary, this study is the first to demonstrate that miR-1827 can regulate osteogenic differentiation. The increase in miR-1827 expression observed during osteogenesis is likely a negative feedback mechanism, thus offering a potential therapeutic target to address inadequate bone volume for dental implantation through inhibiting miR-1827.
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spelling pubmed-53840022017-04-11 miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs Zhu, ShuangXi Peng, Wei Li, Xiang Weng, JunQuan Zhang, Xing Guo, JunBing Huang, DaiYing Rong, Qiong Chen, SongLing Sci Rep Article We recently reported that maxillary sinus membrane stem cells (MSMSCs) have osteogenic potential. However, the biological mechanisms of bone formation remain unclear. In this study, we investigated the role and mechanisms of microRNAs (miRNAs) in the osteogenic differentiation of MSMSCs. The expression of miRNAs was determined in differentiated MSMSCs by comprehensive miRNA microarray analysis and quantitative RT-PCR (qRT-PCR). We selected miR-1827 for functional follow-up studies to explore its significance in MSMSCs. Here, miR-1827 was found to be up-regulated during osteogenic differentiation of MSMSCs. Over expression of miR-1827 inhibited osteogenic differentiation of MSMSCs in vitro, whereas the repression of miR-1827 greatly promoted cell differentiation. Further experiments confirmed that insulin-like growth factor 1 (IGF1) is a direct target of miR-1827. miR-1827 inhibited osteogenic differentiation partially via IGF1, which in turn is a positive regulator of osteogenic differentiation. Moreover, miR-1827 suppressed ectopic bone formation and silencing of miR-1827 led to increased bone formation in vivo. In summary, this study is the first to demonstrate that miR-1827 can regulate osteogenic differentiation. The increase in miR-1827 expression observed during osteogenesis is likely a negative feedback mechanism, thus offering a potential therapeutic target to address inadequate bone volume for dental implantation through inhibiting miR-1827. Nature Publishing Group 2017-04-07 /pmc/articles/PMC5384002/ /pubmed/28387248 http://dx.doi.org/10.1038/srep46136 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhu, ShuangXi
Peng, Wei
Li, Xiang
Weng, JunQuan
Zhang, Xing
Guo, JunBing
Huang, DaiYing
Rong, Qiong
Chen, SongLing
miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs
title miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs
title_full miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs
title_fullStr miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs
title_full_unstemmed miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs
title_short miR-1827 inhibits osteogenic differentiation by targeting IGF1 in MSMSCs
title_sort mir-1827 inhibits osteogenic differentiation by targeting igf1 in msmscs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384002/
https://www.ncbi.nlm.nih.gov/pubmed/28387248
http://dx.doi.org/10.1038/srep46136
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