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

Author:

Niessen Kyle12,Fu YangXin13,Chang Linda12,Hoodless Pamela A.45,McFadden Deborah3,Karsan Aly123

Affiliation:

1. Department of Medical Biophysics, British Columbia Cancer Agency, Vancouver V5Z 1L3, Canada

2. The Experimental Medicine Program

3. The Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver V6T 1Z4, Canada

4. Terry Fox Laboratory, British Columbia Cancer Agency, Vancouver V5Z 1L3, Canada

5. The Department of Medical Genetics, University of British Columbia, Vancouver V6T 1Z4, Canada

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

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