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Rspo1/Wnt signaling promotes angiogenesis via Vegfc/Vegfr3
Author(s) -
Aniket V. Gore,
Matthew Swift,
Ryan M. Young,
Brigid D. Lo,
Mary Cathleen McKinney,
Wenling Li,
Daniel Castranova,
Andrew Davis,
Yohsuke Mukouyama,
Brant M. Weinstein
Publication year - 2011
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.068460
Subject(s) - biology , wnt signaling pathway , angiogenesis , microbiology and biotechnology , endothelial stem cell , lrp5 , vasculogenesis , signal transduction , cancer research , genetics , stem cell , progenitor cell , in vitro
Here, we show that a novel Rspo1-Wnt-Vegfc-Vegfr3 signaling pathway plays an essential role in developmental angiogenesis. A mutation in R-spondin1 (rspo1), a Wnt signaling regulator, was uncovered during a forward-genetic screen for angiogenesis-deficient mutants in the zebrafish. Embryos lacking rspo1 or the proposed rspo1 receptor kremen form primary vessels by vasculogenesis, but are defective in subsequent angiogenesis. Endothelial cell-autonomous inhibition of canonical Wnt signaling also blocks angiogenesis in vivo. The pro-angiogenic effects of Rspo1/Wnt signaling are mediated by Vegfc/Vegfr3(Flt4) signaling. Vegfc expression is dependent on Rspo1 and Wnt, and Vegfc and Vegfr3 are necessary to promote angiogenesis downstream from Rspo1-Wnt. As all of these molecules are expressed by the endothelium during sprouting stages, these results suggest that Rspo1-Wnt-VegfC-Vegfr3 signaling plays a crucial role as an endothelial-autonomous permissive cue for developmental angiogenesis.

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