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Applications of miRNAs in cardiac development, disease progression and regeneration
Development of the complex human heart is tightly regulated at multiple levels, maintaining multipotency and proliferative state in the embryonic cardiovascular progenitors and thereafter suppressing progenitor characteristics to allow for terminal differentiation and maturation. Small regulatory mi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868784/ https://www.ncbi.nlm.nih.gov/pubmed/31752983 http://dx.doi.org/10.1186/s13287-019-1451-2 |
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author | Pang, Jeremy Kah Sheng Phua, Qian Hua Soh, Boon-Seng |
author_facet | Pang, Jeremy Kah Sheng Phua, Qian Hua Soh, Boon-Seng |
author_sort | Pang, Jeremy Kah Sheng |
collection | PubMed |
description | Development of the complex human heart is tightly regulated at multiple levels, maintaining multipotency and proliferative state in the embryonic cardiovascular progenitors and thereafter suppressing progenitor characteristics to allow for terminal differentiation and maturation. Small regulatory microRNAs (miRNAs) are at the level of post-transcriptional gene suppressors, which enhance the degradation or decay of their target protein-coding mRNAs. These miRNAs are known to play roles in a large number of biological events, cardiovascular development being no exception. A number of critical cardiac-specific miRNAs have been identified, of which structural developmental defects have been linked to dysregulation of miRNAs in the proliferating cardiac stem cells. These miRNAs present in the stem cell niche are lost when the cardiac progenitors terminally differentiate, resulting in the postnatal mitotic arrest of the heart. Therapeutic applications of these miRNAs extend to the realm of heart failure, whereby the death of heart cells in the ageing heart cannot be replaced due to the arrest of cell division. By utilizing miRNA therapy to control cell cycling, the regenerative potential of matured myocardium can be restored. This review will address the various cardiac progenitor-related miRNAs that control the development and proliferative potential of the heart. |
format | Online Article Text |
id | pubmed-6868784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68687842019-12-12 Applications of miRNAs in cardiac development, disease progression and regeneration Pang, Jeremy Kah Sheng Phua, Qian Hua Soh, Boon-Seng Stem Cell Res Ther Review Development of the complex human heart is tightly regulated at multiple levels, maintaining multipotency and proliferative state in the embryonic cardiovascular progenitors and thereafter suppressing progenitor characteristics to allow for terminal differentiation and maturation. Small regulatory microRNAs (miRNAs) are at the level of post-transcriptional gene suppressors, which enhance the degradation or decay of their target protein-coding mRNAs. These miRNAs are known to play roles in a large number of biological events, cardiovascular development being no exception. A number of critical cardiac-specific miRNAs have been identified, of which structural developmental defects have been linked to dysregulation of miRNAs in the proliferating cardiac stem cells. These miRNAs present in the stem cell niche are lost when the cardiac progenitors terminally differentiate, resulting in the postnatal mitotic arrest of the heart. Therapeutic applications of these miRNAs extend to the realm of heart failure, whereby the death of heart cells in the ageing heart cannot be replaced due to the arrest of cell division. By utilizing miRNA therapy to control cell cycling, the regenerative potential of matured myocardium can be restored. This review will address the various cardiac progenitor-related miRNAs that control the development and proliferative potential of the heart. BioMed Central 2019-11-21 /pmc/articles/PMC6868784/ /pubmed/31752983 http://dx.doi.org/10.1186/s13287-019-1451-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Pang, Jeremy Kah Sheng Phua, Qian Hua Soh, Boon-Seng Applications of miRNAs in cardiac development, disease progression and regeneration |
title | Applications of miRNAs in cardiac development, disease progression and regeneration |
title_full | Applications of miRNAs in cardiac development, disease progression and regeneration |
title_fullStr | Applications of miRNAs in cardiac development, disease progression and regeneration |
title_full_unstemmed | Applications of miRNAs in cardiac development, disease progression and regeneration |
title_short | Applications of miRNAs in cardiac development, disease progression and regeneration |
title_sort | applications of mirnas in cardiac development, disease progression and regeneration |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868784/ https://www.ncbi.nlm.nih.gov/pubmed/31752983 http://dx.doi.org/10.1186/s13287-019-1451-2 |
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