Slug is a direct Notch target required for initiation of cardiac cushion cellularization
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Open Access
- 28 July 2008
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 182 (2) , 315-325
- https://doi.org/10.1083/jcb.200710067
Abstract
Snail family proteins are key regulators of epithelial-mesenchymal transition, but their role in endothelial-to-mesenchymal transition (EMT) is less well studied. We show that Slug, a Snail family member, is expressed by a subset of endothelial cells as well as mesenchymal cells of the atrioventricular canal and outflow tract during cardiac cushion morphogenesis. Slug deficiency results in impaired cellularization of the cardiac cushion at embryonic day (E)–9.5 but is compensated by increased Snail expression at E10.5, which restores cardiac cushion EMT. We further demonstrate that Slug, but not Snail, is directly up-regulated by Notch in endothelial cells and that Slug expression is required for Notch-mediated repression of the vascular endothelial cadherin promoter and for promoting migration of transformed endothelial cells. In contrast, transforming growth factor β (TGF-β) induces Snail but not Slug. Interestingly, activation of Notch in the context of TGF-β stimulation results in synergistic up-regulation of Snail in endothelial cells. Collectively, our data suggest that combined expression of Slug and Snail is required for EMT in cardiac cushion morphogenesis.Keywords
This publication has 55 references indexed in Scilit:
- Combined Loss of Hey1 and HeyL Causes Congenital Heart Defects Because of Impaired Epithelial to Mesenchymal TransitionCirculation Research, 2007
- Snail family genes are required for left–right asymmetry determination, but not neural crest formation, in miceProceedings of the National Academy of Sciences, 2006
- Snail1 transcriptional repressor binds to its own promoter and controls its expressionNucleic Acids Research, 2006
- Atrioventricular cushion transformation is mediated by ALK2 in the developing mouse heartDevelopmental Biology, 2005
- Mutations in NOTCH1 cause aortic valve diseaseNature, 2005
- The mesenchymal cell, its role in the embryo, and the remarkable signaling mechanisms that create itDevelopmental Dynamics, 2005
- The human VE-cadherin promoter is subjected to organ-specific regulation and is activated in tumour angiogenesisOncogene, 2005
- Notch4 Inhibits Endothelial Apoptosis via RBP-Jκ-dependent and -independent PathwaysJournal of Biological Chemistry, 2004
- The slug gene is not essential for mesoderm or neural crest development in miceDevelopmental Biology, 1998
- Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1Nature Genetics, 1997