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Continuous addition of progenitors forms the cardiac ventricle in zebrafish
The vertebrate heart develops from several progenitor lineages. After early-differentiating first heart field (FHF) progenitors form the linear heart tube, late-differentiating second heart field (SHF) progenitors extend the atrium and ventricle, and form inflow and outflow tracts (IFT/OFT). However...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5962599/ https://www.ncbi.nlm.nih.gov/pubmed/29784942 http://dx.doi.org/10.1038/s41467-018-04402-6 |
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author | Felker, Anastasia Prummel, Karin D. Merks, Anne M. Mickoleit, Michaela Brombacher, Eline C. Huisken, Jan Panáková, Daniela Mosimann, Christian |
author_facet | Felker, Anastasia Prummel, Karin D. Merks, Anne M. Mickoleit, Michaela Brombacher, Eline C. Huisken, Jan Panáková, Daniela Mosimann, Christian |
author_sort | Felker, Anastasia |
collection | PubMed |
description | The vertebrate heart develops from several progenitor lineages. After early-differentiating first heart field (FHF) progenitors form the linear heart tube, late-differentiating second heart field (SHF) progenitors extend the atrium and ventricle, and form inflow and outflow tracts (IFT/OFT). However, the position and migration of late-differentiating progenitors during heart formation remains unclear. Here, we track zebrafish heart development using transgenics based on the cardiopharyngeal gene tbx1. Live imaging uncovers a tbx1 reporter-expressing cell sheath that continuously disseminates from the lateral plate mesoderm towards the forming heart tube. High-speed imaging and optogenetic lineage tracing corroborates that the zebrafish ventricle forms through continuous addition from the undifferentiated progenitor sheath followed by late-phase accrual of the bulbus arteriosus (BA). FGF inhibition during sheath migration reduces ventricle size and abolishes BA formation, refining the window of FGF action during OFT formation. Our findings consolidate previous end-point analyses and establish zebrafish ventricle formation as a continuous process. |
format | Online Article Text |
id | pubmed-5962599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59625992018-05-24 Continuous addition of progenitors forms the cardiac ventricle in zebrafish Felker, Anastasia Prummel, Karin D. Merks, Anne M. Mickoleit, Michaela Brombacher, Eline C. Huisken, Jan Panáková, Daniela Mosimann, Christian Nat Commun Article The vertebrate heart develops from several progenitor lineages. After early-differentiating first heart field (FHF) progenitors form the linear heart tube, late-differentiating second heart field (SHF) progenitors extend the atrium and ventricle, and form inflow and outflow tracts (IFT/OFT). However, the position and migration of late-differentiating progenitors during heart formation remains unclear. Here, we track zebrafish heart development using transgenics based on the cardiopharyngeal gene tbx1. Live imaging uncovers a tbx1 reporter-expressing cell sheath that continuously disseminates from the lateral plate mesoderm towards the forming heart tube. High-speed imaging and optogenetic lineage tracing corroborates that the zebrafish ventricle forms through continuous addition from the undifferentiated progenitor sheath followed by late-phase accrual of the bulbus arteriosus (BA). FGF inhibition during sheath migration reduces ventricle size and abolishes BA formation, refining the window of FGF action during OFT formation. Our findings consolidate previous end-point analyses and establish zebrafish ventricle formation as a continuous process. Nature Publishing Group UK 2018-05-21 /pmc/articles/PMC5962599/ /pubmed/29784942 http://dx.doi.org/10.1038/s41467-018-04402-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Felker, Anastasia Prummel, Karin D. Merks, Anne M. Mickoleit, Michaela Brombacher, Eline C. Huisken, Jan Panáková, Daniela Mosimann, Christian Continuous addition of progenitors forms the cardiac ventricle in zebrafish |
title | Continuous addition of progenitors forms the cardiac ventricle in zebrafish |
title_full | Continuous addition of progenitors forms the cardiac ventricle in zebrafish |
title_fullStr | Continuous addition of progenitors forms the cardiac ventricle in zebrafish |
title_full_unstemmed | Continuous addition of progenitors forms the cardiac ventricle in zebrafish |
title_short | Continuous addition of progenitors forms the cardiac ventricle in zebrafish |
title_sort | continuous addition of progenitors forms the cardiac ventricle in zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5962599/ https://www.ncbi.nlm.nih.gov/pubmed/29784942 http://dx.doi.org/10.1038/s41467-018-04402-6 |
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