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Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish

Heart valve development is governed by both genetic and biomechanical inputs. Prior work has demonstrated that oscillating shear stress associated with blood flow is required for normal atrioventricular (AV) valve development. Cardiac afterload is defined as the pressure the ventricle must overcome...

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Autores principales: Ahuja, Neha, Ostwald, Paige, Gendernalik, Alex, Guzzolino, Elena, Pitto, Letizia, Bark, David, Garrity, Deborah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779957/
https://www.ncbi.nlm.nih.gov/pubmed/35050232
http://dx.doi.org/10.3390/jcdd9010022
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author Ahuja, Neha
Ostwald, Paige
Gendernalik, Alex
Guzzolino, Elena
Pitto, Letizia
Bark, David
Garrity, Deborah M.
author_facet Ahuja, Neha
Ostwald, Paige
Gendernalik, Alex
Guzzolino, Elena
Pitto, Letizia
Bark, David
Garrity, Deborah M.
author_sort Ahuja, Neha
collection PubMed
description Heart valve development is governed by both genetic and biomechanical inputs. Prior work has demonstrated that oscillating shear stress associated with blood flow is required for normal atrioventricular (AV) valve development. Cardiac afterload is defined as the pressure the ventricle must overcome in order to pump blood throughout the circulatory system. In human patients, conditions of high afterload can cause valve pathology. Whether high afterload adversely affects embryonic valve development remains poorly understood. Here we describe a zebrafish model exhibiting increased myocardial afterload, caused by vasopressin, a vasoconstrictive drug. We show that the application of vasopressin reliably produces an increase in afterload without directly acting on cardiac tissue in zebrafish embryos. We have found that increased afterload alters the rate of growth of the cardiac chambers and causes remodeling of cardiomyocytes. Consistent with pathology seen in patients with clinically high afterload, we see defects in both the form and the function of the valve leaflets. Our results suggest that valve defects are due to changes in atrioventricular myocyte signaling, rather than pressure directly acting on the endothelial valve leaflet cells. Cardiac afterload should therefore be considered a biomechanical factor that particularly impacts embryonic valve development.
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spelling pubmed-87799572022-01-22 Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish Ahuja, Neha Ostwald, Paige Gendernalik, Alex Guzzolino, Elena Pitto, Letizia Bark, David Garrity, Deborah M. J Cardiovasc Dev Dis Article Heart valve development is governed by both genetic and biomechanical inputs. Prior work has demonstrated that oscillating shear stress associated with blood flow is required for normal atrioventricular (AV) valve development. Cardiac afterload is defined as the pressure the ventricle must overcome in order to pump blood throughout the circulatory system. In human patients, conditions of high afterload can cause valve pathology. Whether high afterload adversely affects embryonic valve development remains poorly understood. Here we describe a zebrafish model exhibiting increased myocardial afterload, caused by vasopressin, a vasoconstrictive drug. We show that the application of vasopressin reliably produces an increase in afterload without directly acting on cardiac tissue in zebrafish embryos. We have found that increased afterload alters the rate of growth of the cardiac chambers and causes remodeling of cardiomyocytes. Consistent with pathology seen in patients with clinically high afterload, we see defects in both the form and the function of the valve leaflets. Our results suggest that valve defects are due to changes in atrioventricular myocyte signaling, rather than pressure directly acting on the endothelial valve leaflet cells. Cardiac afterload should therefore be considered a biomechanical factor that particularly impacts embryonic valve development. MDPI 2022-01-12 /pmc/articles/PMC8779957/ /pubmed/35050232 http://dx.doi.org/10.3390/jcdd9010022 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ahuja, Neha
Ostwald, Paige
Gendernalik, Alex
Guzzolino, Elena
Pitto, Letizia
Bark, David
Garrity, Deborah M.
Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish
title Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish
title_full Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish
title_fullStr Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish
title_full_unstemmed Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish
title_short Myocardial Afterload Is a Key Biomechanical Regulator of Atrioventricular Myocyte Differentiation in Zebrafish
title_sort myocardial afterload is a key biomechanical regulator of atrioventricular myocyte differentiation in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779957/
https://www.ncbi.nlm.nih.gov/pubmed/35050232
http://dx.doi.org/10.3390/jcdd9010022
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