Cargando…

Persistent Ventricle Partitioning in the Adult Zebrafish Heart

The vertebrate heart integrates cells from the early-differentiating first heart field (FHF) and the later-differentiating second heart field (SHF), both emerging from the lateral plate mesoderm. In mammals, this process forms the basis for the development of the left and right ventricle chambers an...

Descripción completa

Detalles Bibliográficos
Autores principales: Pfefferli, Catherine, Moran, Hannah R., Felker, Anastasia, Mosimann, Christian, Jaźwińska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070482/
https://www.ncbi.nlm.nih.gov/pubmed/33918756
http://dx.doi.org/10.3390/jcdd8040041
_version_ 1783683480404623360
author Pfefferli, Catherine
Moran, Hannah R.
Felker, Anastasia
Mosimann, Christian
Jaźwińska, Anna
author_facet Pfefferli, Catherine
Moran, Hannah R.
Felker, Anastasia
Mosimann, Christian
Jaźwińska, Anna
author_sort Pfefferli, Catherine
collection PubMed
description The vertebrate heart integrates cells from the early-differentiating first heart field (FHF) and the later-differentiating second heart field (SHF), both emerging from the lateral plate mesoderm. In mammals, this process forms the basis for the development of the left and right ventricle chambers and subsequent chamber septation. The single ventricle-forming zebrafish heart also integrates FHF and SHF lineages during embryogenesis, yet the contributions of these two myocardial lineages to the adult zebrafish heart remain incompletely understood. Here, we characterize the myocardial labeling of FHF descendants in both the developing and adult zebrafish ventricle. Expanding previous findings, late gastrulation-stage labeling using drl-driven CreERT2 recombinase with a myocardium-specific, myl7-controlled, loxP reporter results in the predominant labeling of FHF-derived outer curvature and the right side of the embryonic ventricle. Raised to adulthood, such lineage-labeled hearts retain broad areas of FHF cardiomyocytes in a region of the ventricle that is positioned at the opposite side to the atrium and encompasses the apex. Our data add to the increasing evidence for a persisting cell-based compartmentalization of the adult zebrafish ventricle even in the absence of any physical boundary.
format Online
Article
Text
id pubmed-8070482
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-80704822021-04-26 Persistent Ventricle Partitioning in the Adult Zebrafish Heart Pfefferli, Catherine Moran, Hannah R. Felker, Anastasia Mosimann, Christian Jaźwińska, Anna J Cardiovasc Dev Dis Article The vertebrate heart integrates cells from the early-differentiating first heart field (FHF) and the later-differentiating second heart field (SHF), both emerging from the lateral plate mesoderm. In mammals, this process forms the basis for the development of the left and right ventricle chambers and subsequent chamber septation. The single ventricle-forming zebrafish heart also integrates FHF and SHF lineages during embryogenesis, yet the contributions of these two myocardial lineages to the adult zebrafish heart remain incompletely understood. Here, we characterize the myocardial labeling of FHF descendants in both the developing and adult zebrafish ventricle. Expanding previous findings, late gastrulation-stage labeling using drl-driven CreERT2 recombinase with a myocardium-specific, myl7-controlled, loxP reporter results in the predominant labeling of FHF-derived outer curvature and the right side of the embryonic ventricle. Raised to adulthood, such lineage-labeled hearts retain broad areas of FHF cardiomyocytes in a region of the ventricle that is positioned at the opposite side to the atrium and encompasses the apex. Our data add to the increasing evidence for a persisting cell-based compartmentalization of the adult zebrafish ventricle even in the absence of any physical boundary. MDPI 2021-04-09 /pmc/articles/PMC8070482/ /pubmed/33918756 http://dx.doi.org/10.3390/jcdd8040041 Text en © 2021 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
Pfefferli, Catherine
Moran, Hannah R.
Felker, Anastasia
Mosimann, Christian
Jaźwińska, Anna
Persistent Ventricle Partitioning in the Adult Zebrafish Heart
title Persistent Ventricle Partitioning in the Adult Zebrafish Heart
title_full Persistent Ventricle Partitioning in the Adult Zebrafish Heart
title_fullStr Persistent Ventricle Partitioning in the Adult Zebrafish Heart
title_full_unstemmed Persistent Ventricle Partitioning in the Adult Zebrafish Heart
title_short Persistent Ventricle Partitioning in the Adult Zebrafish Heart
title_sort persistent ventricle partitioning in the adult zebrafish heart
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070482/
https://www.ncbi.nlm.nih.gov/pubmed/33918756
http://dx.doi.org/10.3390/jcdd8040041
work_keys_str_mv AT pfefferlicatherine persistentventriclepartitioningintheadultzebrafishheart
AT moranhannahr persistentventriclepartitioningintheadultzebrafishheart
AT felkeranastasia persistentventriclepartitioningintheadultzebrafishheart
AT mosimannchristian persistentventriclepartitioningintheadultzebrafishheart
AT jazwinskaanna persistentventriclepartitioningintheadultzebrafishheart