Tgfβ/Alk5 Signaling Is Required for Shear Stress Induced Klf2 Expression in Embryonic Endothelial Cells

Anastasia D. Egorova, Kim Van der Heiden, Simone Van de Pas, Peter Vennemann, Christian Poelma, Marco C. DeRuiter, Marie-Jose T. H. Goumans, Adriana C. Gittenberger-de Groot, Peter ten Dijke, Robert E. Poelmann, Beerend P. Hierck*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Endothelial cells (EC) translate biomechanical forces into functional and phenotypic responses that play important roles in cardiac development. Specifically, EC in areas of high shear stress, i.e., in the cardiac outflow tract and atrioventricular canal, are characterized by high expression of Kruppel-like factor 2 (Klf2) and by transforming growth factor-beta (Tgf beta)-driven endothelial-to-mesenchymal transition. Extraembryonic venous obstruction (venous clip model) results in congenital heart malformations, and venous clip-induced alterations in shear stress-related gene expression are suggestive for an increase in cardiac shear stress. Here, we study the effects of shear stress on Klf2 expression and Tgf beta-associated signaling in embryonic EC in vivo using the venous clip model and in vitro by subjecting cultured EC to fluid flow. Cellular responses were assessed by analysis of Klf2, Tgf beta ligands, and their downstream signaling targets. Results show that, in embryonic EC, shear stress activates Tgf beta/Alk5 signaling and that induction of Klf2 is an Alk5 dependent process. Developmental Dynamics 240: 1670-1680, 2011. (C) 2011 Wiley-Liss, Inc.
Original languageEnglish
Pages (from-to)1670-1680
Number of pages11
JournalDevelopmental Dynamics
Volume240
Issue number7
DOIs
Publication statusPublished - Jul 2011
Externally publishedYes

Keywords

  • Alk5
  • Klf2
  • Tgf beta
  • Cardiac cushions
  • Endothelium
  • Shear stress

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