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Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects

Innovative research on the interactions between biomechanical load and cardiovascular (CV) morphogenesis by multiple investigators over the past 3 decades, including the application of bioengineering approaches, has shown that the embryonic heart adapts both structure and function in order to mainta...

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Autores principales: Kowalski, William J., Pekkan, Kerem, Tinney, Joseph P., Keller, Bradley B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204442/
https://www.ncbi.nlm.nih.gov/pubmed/25374544
http://dx.doi.org/10.3389/fphys.2014.00408
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author Kowalski, William J.
Pekkan, Kerem
Tinney, Joseph P.
Keller, Bradley B.
author_facet Kowalski, William J.
Pekkan, Kerem
Tinney, Joseph P.
Keller, Bradley B.
author_sort Kowalski, William J.
collection PubMed
description Innovative research on the interactions between biomechanical load and cardiovascular (CV) morphogenesis by multiple investigators over the past 3 decades, including the application of bioengineering approaches, has shown that the embryonic heart adapts both structure and function in order to maintain cardiac output to the rapidly growing embryo. Acute adaptive hemodynamic mechanisms in the embryo include the redistribution of blood flow within the heart, dynamic adjustments in heart rate and developed pressure, and beat to beat variations in blood flow and vascular resistance. These biomechanically relevant events occur coincident with adaptive changes in gene expression and trigger adaptive mechanisms that include alterations in myocardial cell growth and death, regional and global changes in myocardial architecture, and alterations in central vascular morphogenesis and remodeling. These adaptive mechanisms allow the embryo to survive these biomechanical stresses (environmental, maternal) and to compensate for developmental errors (genetic). Recent work from numerous laboratories shows that a subset of these adaptive mechanisms is present in every developing multicellular organism with a “heart” equivalent structure. This chapter will provide the reader with an overview of some of the approaches used to quantify embryonic CV functional maturation and performance, provide several illustrations of experimental interventions that explore the role of biomechanics in the regulation of CV morphogenesis including the role of computational modeling, and identify several critical areas for future investigation as available experimental models and methods expand.
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spelling pubmed-42044422014-11-05 Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects Kowalski, William J. Pekkan, Kerem Tinney, Joseph P. Keller, Bradley B. Front Physiol Physics Innovative research on the interactions between biomechanical load and cardiovascular (CV) morphogenesis by multiple investigators over the past 3 decades, including the application of bioengineering approaches, has shown that the embryonic heart adapts both structure and function in order to maintain cardiac output to the rapidly growing embryo. Acute adaptive hemodynamic mechanisms in the embryo include the redistribution of blood flow within the heart, dynamic adjustments in heart rate and developed pressure, and beat to beat variations in blood flow and vascular resistance. These biomechanically relevant events occur coincident with adaptive changes in gene expression and trigger adaptive mechanisms that include alterations in myocardial cell growth and death, regional and global changes in myocardial architecture, and alterations in central vascular morphogenesis and remodeling. These adaptive mechanisms allow the embryo to survive these biomechanical stresses (environmental, maternal) and to compensate for developmental errors (genetic). Recent work from numerous laboratories shows that a subset of these adaptive mechanisms is present in every developing multicellular organism with a “heart” equivalent structure. This chapter will provide the reader with an overview of some of the approaches used to quantify embryonic CV functional maturation and performance, provide several illustrations of experimental interventions that explore the role of biomechanics in the regulation of CV morphogenesis including the role of computational modeling, and identify several critical areas for future investigation as available experimental models and methods expand. Frontiers Media S.A. 2014-10-21 /pmc/articles/PMC4204442/ /pubmed/25374544 http://dx.doi.org/10.3389/fphys.2014.00408 Text en Copyright © 2014 Kowalski, Pekkan, Tinney and Keller. http://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) or licensor 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 Physics
Kowalski, William J.
Pekkan, Kerem
Tinney, Joseph P.
Keller, Bradley B.
Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
title Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
title_full Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
title_fullStr Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
title_full_unstemmed Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
title_short Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
title_sort investigating developmental cardiovascular biomechanics and the origins of congenital heart defects
topic Physics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204442/
https://www.ncbi.nlm.nih.gov/pubmed/25374544
http://dx.doi.org/10.3389/fphys.2014.00408
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