| Literature DB >> 26766444 |
Beate Scholz1, Claudia Korn2, Jessica Wojtarowicz1, Carolin Mogler3, Iris Augustin4, Michael Boutros4, Christof Niehrs5, Hellmut G Augustin6.
Abstract
The WNT signaling enhancer R-spondin3 (RSPO3) is prominently expressed in the vasculature. Correspondingly, embryonic lethality of Rspo3-deficient mice is caused by vessel remodeling defects. Yet the mechanisms underlying vascular RSPO3 function remain elusive. Inducible endothelial Rspo3 deletion (Rspo3-iECKO) resulted in perturbed developmental and tumor vascular remodeling. Endothelial cell apoptosis and vascular pruning led to reduced microvessel density in Rspo3-iECKO mice. Rspo3-iECKO mice strikingly phenocopied the non-canonical WNT signaling-induced vascular defects of mice deleted for the WNT secretion factor Evi/Wls. An endothelial screen for RSPO3 and EVI/WLS co-regulated genes identified Rnf213, Usp18, and Trim30α. RNF213 targets filamin A and NFAT1 for proteasomal degradation attenuating non-canonical WNT/Ca(2+) signaling. Likewise, USP18 and TRIM5α inhibited NFAT1 activation. Consequently, NFAT protein levels were decreased in endothelial cells of Rspo3-iECKO mice and pharmacological NFAT inhibition phenocopied Rspo3-iECKO mice. The data identify endothelial RSPO3-driven non-canonical WNT/Ca(2+)/NFAT signaling as a critical maintenance pathway of the remodeling vasculature.Entities:
Keywords: Moyamoya; NFAT; R-spondin; RNF213; RSPO3; WNT; angiogenesis; non-canonical WNT pathway; vascular pruning; vascular regression; vascular remodeling
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Year: 2016 PMID: 26766444 DOI: 10.1016/j.devcel.2015.12.015
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270