Department of Biochemistry, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
FEBS Lett. 2012 Apr 5;586(7):1067-72. doi: 10.1016/j.febslet.2012.03.007. Epub 2012 Mar 13.
Vasohibin is thought to be an important negative feedback regulator of angiogenesis that is selectively induced in endothelial cells by VEGF. Here, we assessed the role of vasohibin on HIF-1α expression under oxidative stress induced by hydrogen peroxide (H₂O₂) in HUVEC. VEGF induced significant cell growth that was associated with an increase in vasohibin expression. Following H₂O₂-pretreatment, VEGF further increased cell growth but this was contrastingly associated with a decrease in vasohibin expression when compared with VEGF alone. Interestingly, vasohibin inhibited cell proliferation through degradation of HIF-1α expression during H₂O₂-pretreatment. Furthermore, vasohibin elevated the expression of prolyl hydroxylase (PHD). These results suggest that vasohibin plays crucial roles as a negative feedback regulator of angiogenesis through HIF-1α degradation via PHD.
血管抑素被认为是血管生成的重要负反馈调节因子,它可被 VEGF 选择性地诱导在内皮细胞中表达。在这里,我们评估了血管抑素在过氧化氢(H₂O₂)诱导的人脐静脉内皮细胞(HUVEC)氧化应激下对 HIF-1α表达的作用。VEGF 诱导了显著的细胞生长,这与血管抑素表达的增加有关。在 H₂O₂预处理后,VEGF 进一步增加了细胞生长,但与单独使用 VEGF 相比,这与血管抑素表达的降低形成对比。有趣的是,血管抑素通过在 H₂O₂预处理期间降解 HIF-1α表达来抑制细胞增殖。此外,血管抑素还升高了脯氨酰羟化酶(PHD)的表达。这些结果表明,血管抑素通过 PHD 降解 HIF-1α 作为血管生成的负反馈调节剂发挥关键作用。