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Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process

Organ laterality refers to the left-right asymmetry in disposition and conformation of internal organs and is established during embryogenesis. The heart is the first organ to display visible left-right asymmetries through its left-sided positioning and rightward looping. Here, we present a new zebr...

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Autores principales: Tessadori, Federico, Tsingos, Erika, Colizzi, Enrico Sandro, Kruse, Fabian, van den Brink, Susanne C, van den Boogaard, Malou, Christoffels, Vincent M, Merks, Roeland MH, Bakkers, Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354640/
https://www.ncbi.nlm.nih.gov/pubmed/34372968
http://dx.doi.org/10.7554/eLife.61733
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author Tessadori, Federico
Tsingos, Erika
Colizzi, Enrico Sandro
Kruse, Fabian
van den Brink, Susanne C
van den Boogaard, Malou
Christoffels, Vincent M
Merks, Roeland MH
Bakkers, Jeroen
author_facet Tessadori, Federico
Tsingos, Erika
Colizzi, Enrico Sandro
Kruse, Fabian
van den Brink, Susanne C
van den Boogaard, Malou
Christoffels, Vincent M
Merks, Roeland MH
Bakkers, Jeroen
author_sort Tessadori, Federico
collection PubMed
description Organ laterality refers to the left-right asymmetry in disposition and conformation of internal organs and is established during embryogenesis. The heart is the first organ to display visible left-right asymmetries through its left-sided positioning and rightward looping. Here, we present a new zebrafish loss-of-function allele for tbx5a, which displays defective rightward cardiac looping morphogenesis. By mapping individual cardiomyocyte behavior during cardiac looping, we establish that ventricular and atrial cardiomyocytes rearrange in distinct directions. As a consequence, the cardiac chambers twist around the atrioventricular canal resulting in torsion of the heart tube, which is compromised in tbx5a mutants. Pharmacological treatment and ex vivo culture establishes that the cardiac twisting depends on intrinsic mechanisms and is independent from cardiac growth. Furthermore, genetic experiments indicate that looping requires proper tissue patterning. We conclude that cardiac looping involves twisting of the chambers around the atrioventricular canal, which requires correct tissue patterning by Tbx5a.
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spelling pubmed-83546402021-08-11 Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process Tessadori, Federico Tsingos, Erika Colizzi, Enrico Sandro Kruse, Fabian van den Brink, Susanne C van den Boogaard, Malou Christoffels, Vincent M Merks, Roeland MH Bakkers, Jeroen eLife Cell Biology Organ laterality refers to the left-right asymmetry in disposition and conformation of internal organs and is established during embryogenesis. The heart is the first organ to display visible left-right asymmetries through its left-sided positioning and rightward looping. Here, we present a new zebrafish loss-of-function allele for tbx5a, which displays defective rightward cardiac looping morphogenesis. By mapping individual cardiomyocyte behavior during cardiac looping, we establish that ventricular and atrial cardiomyocytes rearrange in distinct directions. As a consequence, the cardiac chambers twist around the atrioventricular canal resulting in torsion of the heart tube, which is compromised in tbx5a mutants. Pharmacological treatment and ex vivo culture establishes that the cardiac twisting depends on intrinsic mechanisms and is independent from cardiac growth. Furthermore, genetic experiments indicate that looping requires proper tissue patterning. We conclude that cardiac looping involves twisting of the chambers around the atrioventricular canal, which requires correct tissue patterning by Tbx5a. eLife Sciences Publications, Ltd 2021-08-10 /pmc/articles/PMC8354640/ /pubmed/34372968 http://dx.doi.org/10.7554/eLife.61733 Text en © 2021, Tessadori et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Tessadori, Federico
Tsingos, Erika
Colizzi, Enrico Sandro
Kruse, Fabian
van den Brink, Susanne C
van den Boogaard, Malou
Christoffels, Vincent M
Merks, Roeland MH
Bakkers, Jeroen
Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
title Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
title_full Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
title_fullStr Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
title_full_unstemmed Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
title_short Twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
title_sort twisting of the zebrafish heart tube during cardiac looping is a tbx5-dependent and tissue-intrinsic process
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354640/
https://www.ncbi.nlm.nih.gov/pubmed/34372968
http://dx.doi.org/10.7554/eLife.61733
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