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MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway

Calcific aortic valve disease (CAVD) is the most common heart valve disorder, yet its mechanism remains poorly understood. Valve interstitial cells (VICs) are the prevalent cells in aortic valve and their osteogenic differentiation may be responsible for calcific nodule formation in CAVD pathogenesi...

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Autores principales: Xu, Rongjian, Zhao, Min, Yang, Yun, Huang, Zhuo, Shi, Chunying, Hou, Xianglin, Zhao, Yannan, Chen, Bing, Xiao, Zhifeng, Liu, Jianzhou, Miao, Qi, Dai, Jianwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562804/
https://www.ncbi.nlm.nih.gov/pubmed/28821833
http://dx.doi.org/10.1038/s41598-017-09390-z
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author Xu, Rongjian
Zhao, Min
Yang, Yun
Huang, Zhuo
Shi, Chunying
Hou, Xianglin
Zhao, Yannan
Chen, Bing
Xiao, Zhifeng
Liu, Jianzhou
Miao, Qi
Dai, Jianwu
author_facet Xu, Rongjian
Zhao, Min
Yang, Yun
Huang, Zhuo
Shi, Chunying
Hou, Xianglin
Zhao, Yannan
Chen, Bing
Xiao, Zhifeng
Liu, Jianzhou
Miao, Qi
Dai, Jianwu
author_sort Xu, Rongjian
collection PubMed
description Calcific aortic valve disease (CAVD) is the most common heart valve disorder, yet its mechanism remains poorly understood. Valve interstitial cells (VICs) are the prevalent cells in aortic valve and their osteogenic differentiation may be responsible for calcific nodule formation in CAVD pathogenesis. Emerging evidence shows microRNA (miRNA, or miR) can function as important regulators of many pathological processes, including osteogenic differentiation. Here, we aimed to explore the function of miR-449c-5p in CAVD pathogenesis. In this study, we demonstrated the role of miR-449c-5p in VICs osteogenesis. MiRNA microarray assay and qRT-PCR results revealed miR-449c-5p was significantly down-regulated in calcified aortic valves compared with non-calcified valves. MiR-449c-5p overexpression inhibited VICs osteogenic differentiation in vitro, whereas down-regulation of miR-449c-5p enhanced the process. Target prediction analysis and dual-luciferase reporter assay confirmed Smad4 was a direct target of miR-449c-5p. Furthermore, knockdown of Smad4 inhibited VICs osteogenic differentiation, similar to the effect observed in up-regulation miR-449c-5p. In addition, animal experiments proved indirectly miR-449c-5p could alleviate aortic valve calcification. Our data suggested miR-449c-5p could function as a new inhibitory regulator of VICs osteogenic differentiation, which may act by targeting Smad4. MiR-449c-5p may be a potential therapeutic target for CAVD.
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spelling pubmed-55628042017-08-21 MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway Xu, Rongjian Zhao, Min Yang, Yun Huang, Zhuo Shi, Chunying Hou, Xianglin Zhao, Yannan Chen, Bing Xiao, Zhifeng Liu, Jianzhou Miao, Qi Dai, Jianwu Sci Rep Article Calcific aortic valve disease (CAVD) is the most common heart valve disorder, yet its mechanism remains poorly understood. Valve interstitial cells (VICs) are the prevalent cells in aortic valve and their osteogenic differentiation may be responsible for calcific nodule formation in CAVD pathogenesis. Emerging evidence shows microRNA (miRNA, or miR) can function as important regulators of many pathological processes, including osteogenic differentiation. Here, we aimed to explore the function of miR-449c-5p in CAVD pathogenesis. In this study, we demonstrated the role of miR-449c-5p in VICs osteogenesis. MiRNA microarray assay and qRT-PCR results revealed miR-449c-5p was significantly down-regulated in calcified aortic valves compared with non-calcified valves. MiR-449c-5p overexpression inhibited VICs osteogenic differentiation in vitro, whereas down-regulation of miR-449c-5p enhanced the process. Target prediction analysis and dual-luciferase reporter assay confirmed Smad4 was a direct target of miR-449c-5p. Furthermore, knockdown of Smad4 inhibited VICs osteogenic differentiation, similar to the effect observed in up-regulation miR-449c-5p. In addition, animal experiments proved indirectly miR-449c-5p could alleviate aortic valve calcification. Our data suggested miR-449c-5p could function as a new inhibitory regulator of VICs osteogenic differentiation, which may act by targeting Smad4. MiR-449c-5p may be a potential therapeutic target for CAVD. Nature Publishing Group UK 2017-08-18 /pmc/articles/PMC5562804/ /pubmed/28821833 http://dx.doi.org/10.1038/s41598-017-09390-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xu, Rongjian
Zhao, Min
Yang, Yun
Huang, Zhuo
Shi, Chunying
Hou, Xianglin
Zhao, Yannan
Chen, Bing
Xiao, Zhifeng
Liu, Jianzhou
Miao, Qi
Dai, Jianwu
MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway
title MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway
title_full MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway
title_fullStr MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway
title_full_unstemmed MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway
title_short MicroRNA-449c-5p inhibits osteogenic differentiation of human VICs through Smad4-mediated pathway
title_sort microrna-449c-5p inhibits osteogenic differentiation of human vics through smad4-mediated pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562804/
https://www.ncbi.nlm.nih.gov/pubmed/28821833
http://dx.doi.org/10.1038/s41598-017-09390-z
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