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Mending a broken heart—targeting cardiomyocyte regeneration: a literature review
BACKGROUND AND OBJECTIVES: Cardiovascular diseases have been the leading cause of death globally for decades. Pharmacological advances targeting the sympathetic nervous system, renin-angiotensin-aldosterone system, and fibrosis slow the progression of diverse cardiovascular diseases. However, ongoin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708497/ https://www.ncbi.nlm.nih.gov/pubmed/36467352 http://dx.doi.org/10.21037/atm-22-2649 |
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author | Jin, Chunna Zhu, Shiyu Zhao, Tingting Deng, Jiewen Xiang, Meixiang Ma, Hong |
author_facet | Jin, Chunna Zhu, Shiyu Zhao, Tingting Deng, Jiewen Xiang, Meixiang Ma, Hong |
author_sort | Jin, Chunna |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Cardiovascular diseases have been the leading cause of death globally for decades. Pharmacological advances targeting the sympathetic nervous system, renin-angiotensin-aldosterone system, and fibrosis slow the progression of diverse cardiovascular diseases. However, ongoing cardiomyocyte loss is inevitable in divergent cardiovascular diseases, eventually leading to heart failure as the end stage. In this review, we focused on the key biomedical findings and underlying principles of cardiomyocyte regeneration. METHODS: Literature regarding the key findings in cardiomyocyte regeneration research, including controversies on the origins of newly formed cardiomyocytes, potential barriers and strategies to heart regeneration, and the key animals, models, and methods applied in the study of heart regeneration, were broadly researched using the PubMed and Web of Science databases. KEY CONTENT AND FINDINGS: In the mammalian heart, cardiomyocytes proliferate during the embryonic and early postnatal stages, while the capability of proliferation disappears in the adult stage. An increasing amount of evidence suggests that cardiomyocytes self-renew at a very limited level and that most newly formed cardiomyocytes originate from pre-existing cardiomyocytes and not cardiac progenitor cells (CPCs). Several potential barriers to heart regeneration have been addressed, including metabolic switch, a large increase in multinucleated and polyploid cardiomyocytes, and alteration in the epigenome and transcriptome. In addition, immune system evolution is also associated with the loss of regenerative capacity. However, the activation of resident cardiomyocytes, somatic cell reprogramming, and direct reprogramming, in addition to the promotion of neovascularization and immune modulation, constitute the new insights into those strategies that can boost cardiac regeneration. CONCLUSIONS: Heart regeneration is one of the most popular fields in cardiovascular research and represents a promising avenue of therapeutics for mending a broken heart. Despite the controversies and challenges, a clearer picture of adult mammalian cardiac regeneration is emerging. |
format | Online Article Text |
id | pubmed-9708497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-97084972022-12-01 Mending a broken heart—targeting cardiomyocyte regeneration: a literature review Jin, Chunna Zhu, Shiyu Zhao, Tingting Deng, Jiewen Xiang, Meixiang Ma, Hong Ann Transl Med Review Article BACKGROUND AND OBJECTIVES: Cardiovascular diseases have been the leading cause of death globally for decades. Pharmacological advances targeting the sympathetic nervous system, renin-angiotensin-aldosterone system, and fibrosis slow the progression of diverse cardiovascular diseases. However, ongoing cardiomyocyte loss is inevitable in divergent cardiovascular diseases, eventually leading to heart failure as the end stage. In this review, we focused on the key biomedical findings and underlying principles of cardiomyocyte regeneration. METHODS: Literature regarding the key findings in cardiomyocyte regeneration research, including controversies on the origins of newly formed cardiomyocytes, potential barriers and strategies to heart regeneration, and the key animals, models, and methods applied in the study of heart regeneration, were broadly researched using the PubMed and Web of Science databases. KEY CONTENT AND FINDINGS: In the mammalian heart, cardiomyocytes proliferate during the embryonic and early postnatal stages, while the capability of proliferation disappears in the adult stage. An increasing amount of evidence suggests that cardiomyocytes self-renew at a very limited level and that most newly formed cardiomyocytes originate from pre-existing cardiomyocytes and not cardiac progenitor cells (CPCs). Several potential barriers to heart regeneration have been addressed, including metabolic switch, a large increase in multinucleated and polyploid cardiomyocytes, and alteration in the epigenome and transcriptome. In addition, immune system evolution is also associated with the loss of regenerative capacity. However, the activation of resident cardiomyocytes, somatic cell reprogramming, and direct reprogramming, in addition to the promotion of neovascularization and immune modulation, constitute the new insights into those strategies that can boost cardiac regeneration. CONCLUSIONS: Heart regeneration is one of the most popular fields in cardiovascular research and represents a promising avenue of therapeutics for mending a broken heart. Despite the controversies and challenges, a clearer picture of adult mammalian cardiac regeneration is emerging. AME Publishing Company 2022-11 /pmc/articles/PMC9708497/ /pubmed/36467352 http://dx.doi.org/10.21037/atm-22-2649 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Article Jin, Chunna Zhu, Shiyu Zhao, Tingting Deng, Jiewen Xiang, Meixiang Ma, Hong Mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
title | Mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
title_full | Mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
title_fullStr | Mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
title_full_unstemmed | Mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
title_short | Mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
title_sort | mending a broken heart—targeting cardiomyocyte regeneration: a literature review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708497/ https://www.ncbi.nlm.nih.gov/pubmed/36467352 http://dx.doi.org/10.21037/atm-22-2649 |
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