Venous identity requires BMP signalling through ALK3.



Neal, Alice, Nornes, Svanhild, Payne, Sophie, Wallace, Marsha D, Fritzsche, Martin, Louphrasitthiphol, Pakavarin, Wilkinson, Robert N, Chouliaras, Kira M, Liu, Ke, Plant, Karen
et al (show 7 more authors) (2019) Venous identity requires BMP signalling through ALK3. Nature communications, 10 (1). p. 453.

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Abstract

Venous endothelial cells are molecularly and functionally distinct from their arterial counterparts. Although veins are often considered the default endothelial state, genetic manipulations can modulate both acquisition and loss of venous fate, suggesting that venous identity is the result of active transcriptional regulation. However, little is known about this process. Here we show that BMP signalling controls venous identity via the ALK3/BMPR1A receptor and SMAD1/SMAD5. Perturbations to TGF-β and BMP signalling in mice and zebrafish result in aberrant vein formation and loss of expression of the venous-specific gene Ephb4, with no effect on arterial identity. Analysis of a venous endothelium-specific enhancer for Ephb4 shows enriched binding of SMAD1/5 and a requirement for SMAD binding motifs. Further, our results demonstrate that BMP/SMAD-mediated Ephb4 expression requires the venous-enriched BMP type I receptor ALK3/BMPR1A. Together, our analysis demonstrates a requirement for BMP signalling in the establishment of Ephb4 expression and the venous vasculature.

Item Type: Article
Uncontrolled Keywords: Veins, Endothelial Cells, Animals, Animals, Genetically Modified, Mice, Transgenic, Mice, Knockout, Zebrafish, Receptor, EphB4, Transforming Growth Factor beta, Zebrafish Proteins, Bone Morphogenetic Proteins, Signal Transduction, Gene Expression Regulation, Developmental, Smad1 Protein, Smad5 Protein, Bone Morphogenetic Protein Receptors, Type I
Depositing User: Symplectic Admin
Date Deposited: 31 Jan 2019 10:29
Last Modified: 19 Jan 2023 01:05
DOI: 10.1038/s41467-019-08315-w
Open Access URL: https://doi.org/10.1038/s41467-019-08315-w
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3032052