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TGF-β Signaling in Endothelial-to-Mesenchymal Transition: The Role of Shear Stress and Primary Cilia

A Presentation from the Keystone Symposium on Epithelial Plasticity and Epithelial to Mesenchymal Transition, Vancouver, Canada, 21 to 26 January 2011.
Science Signaling21 Feb 2012Vol 5, Issue 212p. pt2DOI: 10.1126/scisignal.2002722

Abstract

Endothelial-to-mesenchymal transition (EndoMT) is an instrumental step in the development of valves in the embryonic heart. This process is driven by activation of transforming growth factor–β (TGF-β) signaling and is characterized by the loss of endothelial and gain of mesenchymal phenotype, and by delamination of cells from the surface into the underlying endocardial cushion matrix. The endothelial cells (ECs) overlying the cushions are typically exposed to high blood flow and concomitant shear stress and do not have a primary cilium. Here, we show that shear stress activates TGF-β–Alk5 signaling in ECs, which is necessary for EndoMT in the cushions. Moreover, we show that the absence of a primary cilium is critically important for this transition process.
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References

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Science Signaling
Volume 5 | Issue 212
February 2012

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Authors

Affiliations

Peter ten Dijke*
Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, Netherlands.
Anastasia D. Egorova
Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, Netherlands.
Marie-José T. H. Goumans
Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, Netherlands.
Robert E. Poelmann
Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, Netherlands.
Beerend P. Hierck
Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, Netherlands.

Notes

*
Presenter. E-mail: [email protected]
†Corresponding author. E-mail: [email protected]

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