Slug is a direct Notch target required for initiation of cardiac cushion cellularization

J Cell Biol. 2008 Jul 28;182(2):315-25. doi: 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 beta (TGF-beta) induces Snail but not Slug. Interestingly, activation of Notch in the context of TGF-beta 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Differentiation / genetics
  • Cell Line
  • Cell Movement / genetics
  • Endocardial Cushions / cytology
  • Endocardial Cushions / embryology*
  • Endocardial Cushions / metabolism
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism
  • Gene Expression Regulation, Developmental / genetics
  • Heart / embryology*
  • Humans
  • Mesoderm / cytology
  • Mesoderm / metabolism
  • Organogenesis / genetics*
  • Promoter Regions, Genetic / genetics
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism*
  • Snail Family Transcription Factors
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism
  • Up-Regulation / genetics

Substances

  • Antigens, CD
  • Cadherins
  • NOTCH1 protein, human
  • Receptor, Notch1
  • SNAI1 protein, human
  • Snail Family Transcription Factors
  • Transcription Factors
  • Transforming Growth Factor beta
  • cadherin 5