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miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation
Induction of cardiomyocyte (CM) proliferation is a promising approach for cardiac regeneration following myocardial injury. MicroRNAs (miRs) have been reported to regulate CM proliferation. In particular, miR-449a-5p has been identified to be associated with CM proliferation in previous high through...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673318/ https://www.ncbi.nlm.nih.gov/pubmed/33179102 http://dx.doi.org/10.3892/mmr.2020.11652 |
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author | Li, Bing Wang, Zhi Yang, Fan Huang, Jing Hu, Xingwei Deng, Shiyan Tian, Maobo Si, Xiaoyun |
author_facet | Li, Bing Wang, Zhi Yang, Fan Huang, Jing Hu, Xingwei Deng, Shiyan Tian, Maobo Si, Xiaoyun |
author_sort | Li, Bing |
collection | PubMed |
description | Induction of cardiomyocyte (CM) proliferation is a promising approach for cardiac regeneration following myocardial injury. MicroRNAs (miRs) have been reported to regulate CM proliferation. In particular, miR-449a-5p has been identified to be associated with CM proliferation in previous high throughput functional screening data. However, whether miR-449a-5p regulates CM proliferation has not been thoroughly investigated. This study aimed to explore whether miR-449a-5p modulates CM proliferation and to identify the molecular mechanism via which miR-449a-5p regulates CM proliferation. The current study demonstrated that miR-449a-5p expression levels were significantly increased during heart development. Furthermore, the results suggested that miR-449a-5p mimic inhibited CM proliferation in vitro as determined via immunofluorescence for ki67 and histone H3 phosphorylated at serine 10 (pH3), as well as the numbers of CMs. However, miR-449a-5p knockdown promoted CM proliferation. CDK6 was identified as a direct target gene of miR-449a-5p, and CDK6 mRNA and protein expression was suppressed by miR-449a-5p. Moreover, CDK6 gain-of-function increased CM proliferation. Overexpression of CDK6 also blocked the inhibitory effect of miR-449a-5p on CM proliferation, indicating that CDK6 was a functional target of miR-449a-5p in CM proliferation. In conclusion, miR-449a-5p inhibited CM proliferation by targeting CDK6, which provides a potential molecular target for preventing myocardial injury. |
format | Online Article Text |
id | pubmed-7673318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-76733182020-11-20 miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation Li, Bing Wang, Zhi Yang, Fan Huang, Jing Hu, Xingwei Deng, Shiyan Tian, Maobo Si, Xiaoyun Mol Med Rep Articles Induction of cardiomyocyte (CM) proliferation is a promising approach for cardiac regeneration following myocardial injury. MicroRNAs (miRs) have been reported to regulate CM proliferation. In particular, miR-449a-5p has been identified to be associated with CM proliferation in previous high throughput functional screening data. However, whether miR-449a-5p regulates CM proliferation has not been thoroughly investigated. This study aimed to explore whether miR-449a-5p modulates CM proliferation and to identify the molecular mechanism via which miR-449a-5p regulates CM proliferation. The current study demonstrated that miR-449a-5p expression levels were significantly increased during heart development. Furthermore, the results suggested that miR-449a-5p mimic inhibited CM proliferation in vitro as determined via immunofluorescence for ki67 and histone H3 phosphorylated at serine 10 (pH3), as well as the numbers of CMs. However, miR-449a-5p knockdown promoted CM proliferation. CDK6 was identified as a direct target gene of miR-449a-5p, and CDK6 mRNA and protein expression was suppressed by miR-449a-5p. Moreover, CDK6 gain-of-function increased CM proliferation. Overexpression of CDK6 also blocked the inhibitory effect of miR-449a-5p on CM proliferation, indicating that CDK6 was a functional target of miR-449a-5p in CM proliferation. In conclusion, miR-449a-5p inhibited CM proliferation by targeting CDK6, which provides a potential molecular target for preventing myocardial injury. D.A. Spandidos 2021-01 2020-11-03 /pmc/articles/PMC7673318/ /pubmed/33179102 http://dx.doi.org/10.3892/mmr.2020.11652 Text en Copyright: © Li 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 Li, Bing Wang, Zhi Yang, Fan Huang, Jing Hu, Xingwei Deng, Shiyan Tian, Maobo Si, Xiaoyun miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation |
title | miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation |
title_full | miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation |
title_fullStr | miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation |
title_full_unstemmed | miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation |
title_short | miR-449a-5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation |
title_sort | mir-449a-5p suppresses cdk6 expression to inhibit cardiomyocyte proliferation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673318/ https://www.ncbi.nlm.nih.gov/pubmed/33179102 http://dx.doi.org/10.3892/mmr.2020.11652 |
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