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PMID: 15175246 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Organization of cardiac chamber progenitors in the zebrafish blastula.

Development (Cambridge, England) ·Vol. 131 ·No. 13 ·2004-07-00 ·Pages 3081-91

Keegan BR, Meyer D, Yelon D

Abstract

Organogenesis requires the specification of a variety of cell types and the organization of these cells into a particular three-dimensional configuration. The embryonic vertebrate heart is organized into two major chambers, the ventricle and atrium, each consisting of two tissue layers, the myocardium and endocardium. The cellular and molecular mechanisms responsible for the separation of ventricular and atrial lineages are not well understood. To test models of cardiac chamber specification, we generated a high-resolution fate map of cardiac chamber progenitors in the zebrafish embryo at 40% epiboly, a stage prior to the initiation of gastrulation. Our map reveals a distinct spatial organization of myocardial progenitors: ventricular myocardial progenitors are positioned closer to the margin and to the dorsal midline than are atrial myocardial progenitors. By contrast, ventricular and atrial endocardial progenitors are not spatially organized at this stage. The relative orientations of ventricular and atrial myocardial progenitors before and after gastrulation suggest orderly movements of these populations. Furthermore, the initial positions of myocardial progenitors at 40% epiboly indicate that signals residing at the embryonic margin could influence chamber fate assignment. Indeed, via fate mapping, we demonstrate that Nodal signaling promotes ventricular fate specification near the margin, thereby playing an important early role during myocardial patterning.

MeSH Terms
Animals Blastomeres/metabolism Blastula/metabolism Cell Lineage Endocardium/metabolism Fluorescein/pharmacology Heart/embryology Heart Ventricles/metabolism In Situ Hybridization Myocardium/metabolism Nodal Protein RNA/metabolism Signal Transduction Stem Cells/metabolism Time Factors Transforming Growth Factor beta/metabolism Zebrafish
Chemicals
Nodal Protein Transforming Growth Factor beta RNA Fluorescein
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Keegan Brian R
Developmental Genetics Program and Department of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
Meyer Dirk
Yelon Deborah
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2004-07-00
Epub
2004-00-02
Pages
3081-91
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NHLBI NIH HHS · R01 HL69594 · United States
NICHD NIH HHS · T32HD07520 · United States
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