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Rspo1/Wnt 信号通过 Vegfc/Vegfr3 促进血管生成。

Rspo1/Wnt signaling promotes angiogenesis via Vegfc/Vegfr3.

机构信息

Program in Genomics of Differentiation, National Institute of Child Health and Human Development, National Institutes of Health, 6B/3B309, Bethesda, MD 20892, USA.

出版信息

Development. 2011 Nov;138(22):4875-86. doi: 10.1242/dev.068460. Epub 2011 Oct 17.

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.

摘要

在这里,我们展示了一个新的 Rspo1-Wnt-Vegfc-Vegfr3 信号通路在发育性血管生成中起着至关重要的作用。在斑马鱼中进行血管生成缺陷突变体的正向遗传筛选过程中发现了 R 螺旋重复蛋白 1(R-spondin1,Rspo1)的一个突变,Rspo1 是 Wnt 信号的调节因子。缺乏 rspo1 或假定的 rspo1 受体 kremlin 的胚胎通过血管生成形成初级血管,但随后的血管生成存在缺陷。内皮细胞自主抑制经典 Wnt 信号也会阻止体内的血管生成。Rspo1/Wnt 信号的促血管生成作用是由 Vegfc/Vegfr3(Flt4)信号介导的。Vegfc 表达依赖于 Rspo1 和 Wnt,Vegfc 和 Vegfr3 是促进 Rspo1-Wnt 下游血管生成所必需的。由于所有这些分子在发芽阶段都由内皮细胞表达,因此这些结果表明 Rspo1-Wnt-VegfC-Vegfr3 信号作为发育性血管生成的内皮自主许可信号发挥着至关重要的作用。

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