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Atrial and Sinoatrial Node Development in the Zebrafish Heart

Proper development and function of the vertebrate heart is vital for embryonic and postnatal life. Many congenital heart defects in humans are associated with disruption of genes that direct the formation or maintenance of atrial and pacemaker cardiomyocytes at the venous pole of the heart. Zebrafis...

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Autores principales: Martin, Kendall E., Waxman, Joshua S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914448/
https://www.ncbi.nlm.nih.gov/pubmed/33572147
http://dx.doi.org/10.3390/jcdd8020015
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author Martin, Kendall E.
Waxman, Joshua S.
author_facet Martin, Kendall E.
Waxman, Joshua S.
author_sort Martin, Kendall E.
collection PubMed
description Proper development and function of the vertebrate heart is vital for embryonic and postnatal life. Many congenital heart defects in humans are associated with disruption of genes that direct the formation or maintenance of atrial and pacemaker cardiomyocytes at the venous pole of the heart. Zebrafish are an outstanding model for studying vertebrate cardiogenesis, due to the conservation of molecular mechanisms underlying early heart development, external development, and ease of genetic manipulation. Here, we discuss early developmental mechanisms that instruct appropriate formation of the venous pole in zebrafish embryos. We primarily focus on signals that determine atrial chamber size and the specialized pacemaker cells of the sinoatrial node through directing proper specification and differentiation, as well as contemporary insights into the plasticity and maintenance of cardiomyocyte identity in embryonic zebrafish hearts. Finally, we integrate how these insights into zebrafish cardiogenesis can serve as models for human atrial defects and arrhythmias.
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spelling pubmed-79144482021-03-01 Atrial and Sinoatrial Node Development in the Zebrafish Heart Martin, Kendall E. Waxman, Joshua S. J Cardiovasc Dev Dis Review Proper development and function of the vertebrate heart is vital for embryonic and postnatal life. Many congenital heart defects in humans are associated with disruption of genes that direct the formation or maintenance of atrial and pacemaker cardiomyocytes at the venous pole of the heart. Zebrafish are an outstanding model for studying vertebrate cardiogenesis, due to the conservation of molecular mechanisms underlying early heart development, external development, and ease of genetic manipulation. Here, we discuss early developmental mechanisms that instruct appropriate formation of the venous pole in zebrafish embryos. We primarily focus on signals that determine atrial chamber size and the specialized pacemaker cells of the sinoatrial node through directing proper specification and differentiation, as well as contemporary insights into the plasticity and maintenance of cardiomyocyte identity in embryonic zebrafish hearts. Finally, we integrate how these insights into zebrafish cardiogenesis can serve as models for human atrial defects and arrhythmias. MDPI 2021-02-09 /pmc/articles/PMC7914448/ /pubmed/33572147 http://dx.doi.org/10.3390/jcdd8020015 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Martin, Kendall E.
Waxman, Joshua S.
Atrial and Sinoatrial Node Development in the Zebrafish Heart
title Atrial and Sinoatrial Node Development in the Zebrafish Heart
title_full Atrial and Sinoatrial Node Development in the Zebrafish Heart
title_fullStr Atrial and Sinoatrial Node Development in the Zebrafish Heart
title_full_unstemmed Atrial and Sinoatrial Node Development in the Zebrafish Heart
title_short Atrial and Sinoatrial Node Development in the Zebrafish Heart
title_sort atrial and sinoatrial node development in the zebrafish heart
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914448/
https://www.ncbi.nlm.nih.gov/pubmed/33572147
http://dx.doi.org/10.3390/jcdd8020015
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