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A Snail1/Notch1 signalling axis controls embryonic vascular development.
- Source :
-
Nature communications [Nat Commun] 2014 Jun 04; Vol. 5, pp. 3998. Date of Electronic Publication: 2014 Jun 04. - Publication Year :
- 2014
-
Abstract
- Notch1-Delta-like 4 (Dll4) signalling controls vascular development by regulating endothelial cell (EC) targets that modulate vessel wall remodelling and arterial-venous specification. The molecular effectors that modulate Notch signalling during vascular development remain largely undefined. Here we demonstrate that the transcriptional repressor, Snail1, acts as a VEGF-induced regulator of Notch1 signalling and Dll4 expression. EC-specific Snail1 loss-of-function conditional knockout mice die in utero with defects in vessel wall remodelling in association with losses in mural cell investment and disruptions in arterial-venous specification. Snail1 loss-of-function conditional knockout embryos further display upregulated Notch1 signalling and Dll4 expression that is partially reversed by inhibiting γ-secretase activity in vivo with Dll4 identified as a direct target of Snail1-mediated transcriptional repression. These results document a Snail1-Dll4/Notch1 axis that controls embryonic vascular development.
- Subjects :
- Adaptor Proteins, Signal Transducing
Animals
Calcium-Binding Proteins
Epithelial-Mesenchymal Transition
Feedback, Physiological
In Vitro Techniques
Mice
Mice, Knockout
Signal Transduction
Snail Family Transcription Factors
Transcription Factors metabolism
Vascular Remodeling genetics
Blood Vessels embryology
Endothelial Cells metabolism
Intracellular Signaling Peptides and Proteins metabolism
Membrane Proteins metabolism
Receptor, Notch1 metabolism
Transcription Factors genetics
Vascular Endothelial Growth Factor A metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 24894949
- Full Text :
- https://doi.org/10.1038/ncomms4998