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Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary

Follicular atresia mainly results from the apoptosis of granulosa cells (GCs). Whilst our previous investigations examined the role of chi-miR-4110 in regulating ovarian function, the present study detected the role of chi-miR-4110 in GC development. We transfected caprine GCs cultured in vitro with...

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Autores principales: An, Xiaopeng, Song, Yuxuan, Hou, Jinxing, Zhang, Yue, Chen, Kaiwen, Ma, Haidong, Zhao, Xinyan, Li, Guang, Gao, Kexin, Wang, Shan, Cao, Binyun, Bai, Yueyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509297/
https://www.ncbi.nlm.nih.gov/pubmed/28704526
http://dx.doi.org/10.1371/journal.pone.0181162
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author An, Xiaopeng
Song, Yuxuan
Hou, Jinxing
Zhang, Yue
Chen, Kaiwen
Ma, Haidong
Zhao, Xinyan
Li, Guang
Gao, Kexin
Wang, Shan
Cao, Binyun
Bai, Yueyu
author_facet An, Xiaopeng
Song, Yuxuan
Hou, Jinxing
Zhang, Yue
Chen, Kaiwen
Ma, Haidong
Zhao, Xinyan
Li, Guang
Gao, Kexin
Wang, Shan
Cao, Binyun
Bai, Yueyu
author_sort An, Xiaopeng
collection PubMed
description Follicular atresia mainly results from the apoptosis of granulosa cells (GCs). Whilst our previous investigations examined the role of chi-miR-4110 in regulating ovarian function, the present study detected the role of chi-miR-4110 in GC development. We transfected caprine GCs cultured in vitro with chi-miR-4110 mimics. Results revealed that chi-miR-4110 decreased mRNA and protein levels of Smad2 by targeting its 3′-untranslated region (3′UTR). FoxC1 and Sp1 mRNA and protein levels markedly increased, whereas those of bHLHe22 significantly decreased (P<0.01 or 0.05) in GCs transfected with the chi-miR-4110 mimics. Further studies revealed a significantly higher number of apoptotic cells in GCs transfected with the chi-miR-4110 mimics (P< 0.05) than in GCs transfected with mimics negative control. GCs transfected with the chi-miR-4110 mimics exhibited significantly increased mRNA and protein levels of the pro-apoptotic gene Bax (P<0.01) and significantly decreased expression levels of the anti-apoptotic gene BCL-2 (P<0.01). Smad2 interference (Si-1282) results were consistent with those of the chi-miR-4110 mimics. Previous reports and our results showed that chi-miR-4110 increases Sp1 expression by repressing Smad2. The increase in Sp1 induces p53-upregulated modulator of apoptosis, which increases the relative abundance of Bax and causes caprine GC apoptosis. Our findings may provide relevant data for the investigation of miRNA-mediated regulation of ovarian functions.
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spelling pubmed-55092972017-08-07 Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary An, Xiaopeng Song, Yuxuan Hou, Jinxing Zhang, Yue Chen, Kaiwen Ma, Haidong Zhao, Xinyan Li, Guang Gao, Kexin Wang, Shan Cao, Binyun Bai, Yueyu PLoS One Research Article Follicular atresia mainly results from the apoptosis of granulosa cells (GCs). Whilst our previous investigations examined the role of chi-miR-4110 in regulating ovarian function, the present study detected the role of chi-miR-4110 in GC development. We transfected caprine GCs cultured in vitro with chi-miR-4110 mimics. Results revealed that chi-miR-4110 decreased mRNA and protein levels of Smad2 by targeting its 3′-untranslated region (3′UTR). FoxC1 and Sp1 mRNA and protein levels markedly increased, whereas those of bHLHe22 significantly decreased (P<0.01 or 0.05) in GCs transfected with the chi-miR-4110 mimics. Further studies revealed a significantly higher number of apoptotic cells in GCs transfected with the chi-miR-4110 mimics (P< 0.05) than in GCs transfected with mimics negative control. GCs transfected with the chi-miR-4110 mimics exhibited significantly increased mRNA and protein levels of the pro-apoptotic gene Bax (P<0.01) and significantly decreased expression levels of the anti-apoptotic gene BCL-2 (P<0.01). Smad2 interference (Si-1282) results were consistent with those of the chi-miR-4110 mimics. Previous reports and our results showed that chi-miR-4110 increases Sp1 expression by repressing Smad2. The increase in Sp1 induces p53-upregulated modulator of apoptosis, which increases the relative abundance of Bax and causes caprine GC apoptosis. Our findings may provide relevant data for the investigation of miRNA-mediated regulation of ovarian functions. Public Library of Science 2017-07-13 /pmc/articles/PMC5509297/ /pubmed/28704526 http://dx.doi.org/10.1371/journal.pone.0181162 Text en © 2017 An et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
An, Xiaopeng
Song, Yuxuan
Hou, Jinxing
Zhang, Yue
Chen, Kaiwen
Ma, Haidong
Zhao, Xinyan
Li, Guang
Gao, Kexin
Wang, Shan
Cao, Binyun
Bai, Yueyu
Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary
title Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary
title_full Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary
title_fullStr Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary
title_full_unstemmed Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary
title_short Chi-miR-4110 promotes granulosa cell apoptosis by targeting Sma- and Mad-related protein 2 (Smad2) in the caprine ovary
title_sort chi-mir-4110 promotes granulosa cell apoptosis by targeting sma- and mad-related protein 2 (smad2) in the caprine ovary
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509297/
https://www.ncbi.nlm.nih.gov/pubmed/28704526
http://dx.doi.org/10.1371/journal.pone.0181162
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