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MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e
Accumulating evidence demonstrated that miRNAs are highly involved in kidney fibrosis and Epithelial-Eesenchymal Transition (EMT), however, the mechanisms of miRNAs in kidney fibrosis are poorly understood. In this work, we identified that miR542-3p could promote EMT through down-regulating bone mor...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661932/ https://www.ncbi.nlm.nih.gov/pubmed/26610487 http://dx.doi.org/10.3390/ijms161126075 |
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author | Liu, Zhicheng Zhou, Yuru Yuan, Yue Nie, Fang Peng, Rui Li, Qianyin Lyu, Zhongshi Mao, Zhaomin Huang, Liyuan Zhou, Li Li, Yiman Hao, Jing Ni, Dongsheng Jin, Qianni Long, Yaoshui Ju, Pan Yu, Wen Liu, Jianing Hu, Yanxia Zhou, Qin |
author_facet | Liu, Zhicheng Zhou, Yuru Yuan, Yue Nie, Fang Peng, Rui Li, Qianyin Lyu, Zhongshi Mao, Zhaomin Huang, Liyuan Zhou, Li Li, Yiman Hao, Jing Ni, Dongsheng Jin, Qianni Long, Yaoshui Ju, Pan Yu, Wen Liu, Jianing Hu, Yanxia Zhou, Qin |
author_sort | Liu, Zhicheng |
collection | PubMed |
description | Accumulating evidence demonstrated that miRNAs are highly involved in kidney fibrosis and Epithelial-Eesenchymal Transition (EMT), however, the mechanisms of miRNAs in kidney fibrosis are poorly understood. In this work, we identified that miR542-3p could promote EMT through down-regulating bone morphogenetic protein 7 (BMP7) expression by targeting BMP7 3′UTR. Firstly, real-time PCR results showed that miR542-3p was significantly up-regulated in kidney fibrosis in vitro and in vivo. Moreover, Western blot results demonstrated that miR542-3p may promote EMT in the NRK52e cell line. In addition, we confirmed that BMP7, which played a crucial role in anti-kidney fibrosis and suppressed the progression of EMT, was a target of miR542-3p through Dual-Luciferase reporter assay, as did Western blot analysis. The effects of miR542-3p on regulating EMT could also be suppressed by transiently overexpressing BMP7 in NRK52e cells. Taken together, miR542-3p may be a critical mediator of the induction of EMT via directly targeting BMP7. |
format | Online Article Text |
id | pubmed-4661932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-46619322015-12-10 MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e Liu, Zhicheng Zhou, Yuru Yuan, Yue Nie, Fang Peng, Rui Li, Qianyin Lyu, Zhongshi Mao, Zhaomin Huang, Liyuan Zhou, Li Li, Yiman Hao, Jing Ni, Dongsheng Jin, Qianni Long, Yaoshui Ju, Pan Yu, Wen Liu, Jianing Hu, Yanxia Zhou, Qin Int J Mol Sci Article Accumulating evidence demonstrated that miRNAs are highly involved in kidney fibrosis and Epithelial-Eesenchymal Transition (EMT), however, the mechanisms of miRNAs in kidney fibrosis are poorly understood. In this work, we identified that miR542-3p could promote EMT through down-regulating bone morphogenetic protein 7 (BMP7) expression by targeting BMP7 3′UTR. Firstly, real-time PCR results showed that miR542-3p was significantly up-regulated in kidney fibrosis in vitro and in vivo. Moreover, Western blot results demonstrated that miR542-3p may promote EMT in the NRK52e cell line. In addition, we confirmed that BMP7, which played a crucial role in anti-kidney fibrosis and suppressed the progression of EMT, was a target of miR542-3p through Dual-Luciferase reporter assay, as did Western blot analysis. The effects of miR542-3p on regulating EMT could also be suppressed by transiently overexpressing BMP7 in NRK52e cells. Taken together, miR542-3p may be a critical mediator of the induction of EMT via directly targeting BMP7. MDPI 2015-11-24 /pmc/articles/PMC4661932/ /pubmed/26610487 http://dx.doi.org/10.3390/ijms161126075 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Zhicheng Zhou, Yuru Yuan, Yue Nie, Fang Peng, Rui Li, Qianyin Lyu, Zhongshi Mao, Zhaomin Huang, Liyuan Zhou, Li Li, Yiman Hao, Jing Ni, Dongsheng Jin, Qianni Long, Yaoshui Ju, Pan Yu, Wen Liu, Jianing Hu, Yanxia Zhou, Qin MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e |
title | MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e |
title_full | MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e |
title_fullStr | MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e |
title_full_unstemmed | MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e |
title_short | MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e |
title_sort | mir542-3p regulates the epithelial-mesenchymal transition by directly targeting bmp7 in nrk52e |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661932/ https://www.ncbi.nlm.nih.gov/pubmed/26610487 http://dx.doi.org/10.3390/ijms161126075 |
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