Zheng Hong, Wasylyk Christine, Ayadi Abdelkader, Abecassis Joseph, Schalken Jack A, Rogatsch Hermann, Wernert Nicolas, Maira Sauveur-Michel, Multon Marie-Christine, Wasylyk Bohdan
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, 67404 Illkirch, France.
Genes Dev. 2003 Sep 15;17(18):2283-97. doi: 10.1101/gad.272503.
Angiogenesis is fundamental to physiological and pathological processes. Despite intensive efforts, little is known about the intracellular circuits that regulate angiogenesis. The transcription factor Net is activated by phosphorylation induced by Ras, an indirect regulator of angiogenesis. Net is expressed at sites of vasculogenesis and angiogenesis during early mouse development, suggesting that it could have a role in blood vessel formation. We show here that down-regulation of Net inhibits angiogenesis and vascular endothelial growth factor (VEGF) expression in vivo, ex vivo, and in vitro. Ras-activated phosphorylated Net (P-Net) stimulates the mouse VEGF promoter through the -80 to -53 region that principally binds Sp1. P-Net and VEGF are coexpressed in angiogenic processes in wild-type mouse tissues and in human tumors. We conclude that Net is a regulator of angiogenesis that can switch to an activator following induction by pro-angiogenic molecules.
血管生成对于生理和病理过程至关重要。尽管进行了大量研究,但对于调节血管生成的细胞内信号通路仍知之甚少。转录因子Net由Ras诱导的磷酸化激活,Ras是血管生成的间接调节因子。在小鼠早期发育过程中,Net在血管发生和血管生成部位表达,这表明它可能在血管形成中发挥作用。我们在此表明,Net的下调在体内、体外和离体条件下均会抑制血管生成和血管内皮生长因子(VEGF)的表达。Ras激活的磷酸化Net(P-Net)通过主要结合Sp1的-80至-53区域刺激小鼠VEGF启动子。P-Net和VEGF在野生型小鼠组织和人类肿瘤的血管生成过程中共同表达。我们得出结论,Net是血管生成的调节因子,在促血管生成分子诱导后可转变为激活剂。