Treins Caroline, Murdaca Joseph, Van Obberghen Emmanuel, Giorgetti-Peraldi Sophie
Institut National de la Santé et de la Recherche Médicale U145, Nice, France.
Biochem Biophys Res Commun. 2006 Apr 21;342(4):1197-202. doi: 10.1016/j.bbrc.2006.02.088. Epub 2006 Feb 24.
Insulin, insulin like growth factor (IGF)-1, and AMP-activated protein kinase (AMPK) signaling regulate independently angiogenesis through vascular endothelial growth factor (VEGF) expression. In the present study, we investigated a potential cross-talk between these signaling pathways on hypoxia-inducible factor (HIF)-1alpha and VEGF expression. Retinal epithelial ARPE-19 cells were treated with AICAR, an AMPK activator, alone or in combination with insulin and IGF-1. AICAR stimulated VEGF mRNA expression, but did not modify the insulin- and IGF-1-induced VEGF expression. We have investigated the effect of AICAR on insulin and IGF-1 signaling pathways. We observed that AICAR increased insulin- and IGF-1-induced phosphorylation of PKB, whereas phosphorylation of S6K-1 was decreased. Moreover, AICAR and metformin inhibited the ability of insulin and IGF-1 to induce HIF-1alpha expression. These results show that AICAR and insulin/IGF-1 regulate VEGF expression through different mechanisms.
胰岛素、胰岛素样生长因子(IGF)-1和AMP激活的蛋白激酶(AMPK)信号通路通过血管内皮生长因子(VEGF)表达独立调节血管生成。在本研究中,我们调查了这些信号通路在缺氧诱导因子(HIF)-1α和VEGF表达上的潜在相互作用。视网膜上皮ARPE-19细胞单独用AMPK激活剂AICAR处理,或与胰岛素和IGF-1联合处理。AICAR刺激VEGF mRNA表达,但不改变胰岛素和IGF-1诱导的VEGF表达。我们研究了AICAR对胰岛素和IGF-1信号通路的影响。我们观察到AICAR增加了胰岛素和IGF-1诱导的蛋白激酶B(PKB)磷酸化,而核糖体蛋白S6激酶1(S6K-1)的磷酸化减少。此外,AICAR和二甲双胍抑制胰岛素和IGF-1诱导HIF-1α表达的能力。这些结果表明,AICAR和胰岛素/IGF-1通过不同机制调节VEGF表达。