
Hey2 regulates the size of the cardiac progenitor pool during vertebrate heart development
Author(s) -
Natalie Gibb,
Savo Lazic,
Xuefei Yuan,
Ashish R. Deshwar,
Meaghan Leslie,
Michael D. Wilson,
Ian C. Scott
Publication year - 2018
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.167510
Subject(s) - biology , progenitor cell , progenitor , zebrafish , heart development , microbiology and biotechnology , cardiac function curve , regeneration (biology) , stem cell , medicine , genetics , heart failure , embryonic stem cell , gene
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.