Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jin, Chunna, Zhu, Shiyu, Zhao, Tingting, Deng, Jiewen, Xiang, Meixiang, Ma, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
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
_version_ 1784840947712917504
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
work_keys_str_mv AT jinchunna mendingabrokenhearttargetingcardiomyocyteregenerationaliteraturereview
AT zhushiyu mendingabrokenhearttargetingcardiomyocyteregenerationaliteraturereview
AT zhaotingting mendingabrokenhearttargetingcardiomyocyteregenerationaliteraturereview
AT dengjiewen mendingabrokenhearttargetingcardiomyocyteregenerationaliteraturereview
AT xiangmeixiang mendingabrokenhearttargetingcardiomyocyteregenerationaliteraturereview
AT mahong mendingabrokenhearttargetingcardiomyocyteregenerationaliteraturereview