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      Rspo1/Wnt signaling promotes angiogenesis via Vegfc/Vegfr3.

      Development (Cambridge, England)
      Animals, Animals, Genetically Modified, Cells, Cultured, Embryo, Nonmammalian, Gene Expression Regulation, Developmental, Models, Biological, Neovascularization, Pathologic, genetics, metabolism, Neovascularization, Physiologic, Up-Regulation, physiology, Vascular Endothelial Growth Factor C, Vascular Endothelial Growth Factor Receptor-3, Wnt Proteins, Wnt Signaling Pathway, Zebrafish, embryology, Zebrafish Proteins

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          Abstract

          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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