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Cardiomyocyte-fibroblast crosstalk in the postnatal heart
During the postnatal period in mammals, the heart undergoes significant remodeling in response to increased circulatory demands. In the days after birth, cardiac cells, including cardiomyocytes and fibroblasts, progressively lose embryonic characteristics concomitant with the loss of the heart’s abi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106698/ https://www.ncbi.nlm.nih.gov/pubmed/37077417 http://dx.doi.org/10.3389/fcell.2023.1163331 |
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author | Uscategui Calderon, Maria Gonzalez, Brittany A. Yutzey, Katherine E. |
author_facet | Uscategui Calderon, Maria Gonzalez, Brittany A. Yutzey, Katherine E. |
author_sort | Uscategui Calderon, Maria |
collection | PubMed |
description | During the postnatal period in mammals, the heart undergoes significant remodeling in response to increased circulatory demands. In the days after birth, cardiac cells, including cardiomyocytes and fibroblasts, progressively lose embryonic characteristics concomitant with the loss of the heart’s ability to regenerate. Moreover, postnatal cardiomyocytes undergo binucleation and cell cycle arrest with induction of hypertrophic growth, while cardiac fibroblasts proliferate and produce extracellular matrix (ECM) that transitions from components that support cellular maturation to production of the mature fibrous skeleton of the heart. Recent studies have implicated interactions of cardiac fibroblasts and cardiomyocytes within the maturing ECM environment to promote heart maturation in the postnatal period. Here, we review the relationships of different cardiac cell types and the ECM as the heart undergoes both structural and functional changes during development. Recent advances in the field, particularly in several recently published transcriptomic datasets, have highlighted specific signaling mechanisms that underlie cellular maturation and demonstrated the biomechanical interdependence of cardiac fibroblast and cardiomyocyte maturation. There is increasing evidence that postnatal heart development in mammals is dependent on particular ECM components and that resulting changes in biomechanics influence cell maturation. These advances, in definition of cardiac fibroblast heterogeneity and function in relation to cardiomyocyte maturation and the extracellular environment provide, support for complex cell crosstalk in the postnatal heart with implications for heart regeneration and disease mechanisms. |
format | Online Article Text |
id | pubmed-10106698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101066982023-04-18 Cardiomyocyte-fibroblast crosstalk in the postnatal heart Uscategui Calderon, Maria Gonzalez, Brittany A. Yutzey, Katherine E. Front Cell Dev Biol Cell and Developmental Biology During the postnatal period in mammals, the heart undergoes significant remodeling in response to increased circulatory demands. In the days after birth, cardiac cells, including cardiomyocytes and fibroblasts, progressively lose embryonic characteristics concomitant with the loss of the heart’s ability to regenerate. Moreover, postnatal cardiomyocytes undergo binucleation and cell cycle arrest with induction of hypertrophic growth, while cardiac fibroblasts proliferate and produce extracellular matrix (ECM) that transitions from components that support cellular maturation to production of the mature fibrous skeleton of the heart. Recent studies have implicated interactions of cardiac fibroblasts and cardiomyocytes within the maturing ECM environment to promote heart maturation in the postnatal period. Here, we review the relationships of different cardiac cell types and the ECM as the heart undergoes both structural and functional changes during development. Recent advances in the field, particularly in several recently published transcriptomic datasets, have highlighted specific signaling mechanisms that underlie cellular maturation and demonstrated the biomechanical interdependence of cardiac fibroblast and cardiomyocyte maturation. There is increasing evidence that postnatal heart development in mammals is dependent on particular ECM components and that resulting changes in biomechanics influence cell maturation. These advances, in definition of cardiac fibroblast heterogeneity and function in relation to cardiomyocyte maturation and the extracellular environment provide, support for complex cell crosstalk in the postnatal heart with implications for heart regeneration and disease mechanisms. Frontiers Media S.A. 2023-04-03 /pmc/articles/PMC10106698/ /pubmed/37077417 http://dx.doi.org/10.3389/fcell.2023.1163331 Text en Copyright © 2023 Uscategui Calderon, Gonzalez and Yutzey. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Uscategui Calderon, Maria Gonzalez, Brittany A. Yutzey, Katherine E. Cardiomyocyte-fibroblast crosstalk in the postnatal heart |
title | Cardiomyocyte-fibroblast crosstalk in the postnatal heart |
title_full | Cardiomyocyte-fibroblast crosstalk in the postnatal heart |
title_fullStr | Cardiomyocyte-fibroblast crosstalk in the postnatal heart |
title_full_unstemmed | Cardiomyocyte-fibroblast crosstalk in the postnatal heart |
title_short | Cardiomyocyte-fibroblast crosstalk in the postnatal heart |
title_sort | cardiomyocyte-fibroblast crosstalk in the postnatal heart |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106698/ https://www.ncbi.nlm.nih.gov/pubmed/37077417 http://dx.doi.org/10.3389/fcell.2023.1163331 |
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