Rspo1/Wnt signaling promotes angiogenesis via Vegfc/Vegfr3

被引:82
|
作者
Gore, Aniket V. [1 ]
Swift, Matthew R. [1 ]
Cha, Young R. [1 ]
Lo, Brigid [1 ]
McKinney, Mary C. [1 ]
Li, Wenling [2 ]
Castranova, Daniel [1 ]
Davis, Andrew [1 ]
Mukouyama, Yoh-suke [2 ]
Weinstein, Brant M. [1 ]
机构
[1] NICHHD, Program Genom Differentiat, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Lab Stem Cell & Neuro Vasc Biol, Genet & Dev Biol Ctr, NIH, Bethesda, MD 20892 USA
来源
DEVELOPMENT | 2011年 / 138卷 / 22期
关键词
Angiogenesis; Vegfc; Zebrafish; ENDOTHELIAL-GROWTH-FACTOR; VASCULAR DEVELOPMENT; DEVELOPING ZEBRAFISH; MOUSE EMBRYOS; VEGF-C; NEGATIVE REGULATOR; WNT; PATHWAY; CELLS; MORPHOGENESIS;
D O I
10.1242/dev.068460
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:4875 / 4886
页数:12
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