PUBLICATION

Hey2 regulates the size of the cardiac progenitor pool during vertebrate heart development

Authors
Gibb, N., Lazic, S., Yuan, X., Deshwar, A.R., Leslie, M., Wilson, M.D., Scott, I.C.
ID
ZDB-PUB-181026-14
Date
2018
Source
Development (Cambridge, England)   145(22): (Journal)
Registered Authors
Deshwar, Ashish, Gibb, Natalie, Lazic, Savo, Leslie, Meaghan, Scott, Ian, Yuan, Xuefei
Keywords
Cardiac progenitors, Heart development, Hey2, Second heart field, Zebrafish
MeSH Terms
  • Heart/embryology*
  • Cell Proliferation
  • Basic Helix-Loop-Helix Transcription Factors/genetics
  • Basic Helix-Loop-Helix Transcription Factors/metabolism*
  • Cell Count
  • Fibroblast Growth Factors/metabolism
  • Cell Lineage
  • Signal Transduction
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
  • Myocardium/metabolism
  • Myocardium/pathology
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish/metabolism*
  • Cardiovascular Diseases/pathology
  • Mutation/genetics
  • Myocytes, Cardiac/metabolism
  • Myocytes, Cardiac/pathology
  • Cell Size
  • Gene Expression Regulation, Developmental
  • Stem Cells/cytology*
  • Stem Cells/metabolism*
  • Animals
PubMed
30355727 Full text @ Development
Abstract
A key event in heart development is the timely addition of cardiac progenitor cells, defects in which can lead to congenital heart defects. However, how the balance and proportion of progenitor proliferation versus addition to the heart is regulated remains poorly understood. Here we demonstrate that Hey2 functions to regulate the dynamics of cardiac progenitor addition to the zebrafish heart. We found that the previously noted increase in myocardial cell number found in the absence of Hey2 function was due to a pronounced expansion in the size of the cardiac progenitor pool. Expression analysis and lineage tracing of hey2-expressing cells showed that hey2 is active in cardiac progenitors. Hey2 acted to limit proliferation of cardiac progenitors, prior to heart tube formation. Use of a transplantation approach demonstrated a likely cell autonomous (in cardiac progenitors) function for Hey2. Taken together, our data suggests a previously unappreciated role for Hey2 in controlling the proliferative capacity of cardiac progenitors, affecting the subsequent contribution of late-differentiating cardiac progenitors to the developing vertebrate heart.
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Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
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Mapping