Baker Nicole, O'Meara Sarah J, Scannell Michael, Maderna Paola, Godson Catherine
School of Medicine and Medical Science, University College Dublin Diabetes Research Centre, UCD Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
J Immunol. 2009 Mar 15;182(6):3819-26. doi: 10.4049/jimmunol.0803175.
Lipoxins (LX) are a class of eicosanoid that possesses a wide spectrum of antiinflammatory and proresolution bioactions. Here we have investigated the impact of the endogenously produced eicosanoid LXA(4) on endothelial cell inflammatory, proliferative, and antigenic responses. Using HUVECs we demonstrate that LXA(4) inhibits vascular endothelial growth factor (VEGF)-stimulated inflammatory responses including IL-6, TNF-alpha, IFN-gamma and IL-8 secretion, as well as endothelial ICAM-1 expression. Interestingly, LXA(4) up-regulated IL-10 production from HUVECs. Consistent with these antiinflammatory and proresolution responses to LXA(4), we demonstrate that LXA(4) inhibited leukotriene D(4) and VEGF-stimulated proliferation and angiogenesis as determined by tube formation of HUVECs. We have explored the underlying molecular mechanisms and demonstrate that LXA(4) pretreatment is associated with the decrease of VEGF-stimulated VEGF receptor 2 (KDR/FLK-1) phosphorylation and downstream signaling events including activation of phospholipase C-gamma, ERK1/2, and Akt.
脂氧素(LX)是一类具有广泛抗炎和促炎症消退生物活性的类花生酸。在此,我们研究了内源性产生的类花生酸LXA(4)对内皮细胞炎症、增殖和抗原反应的影响。利用人脐静脉内皮细胞(HUVECs),我们证明LXA(4)抑制血管内皮生长因子(VEGF)刺激的炎症反应,包括白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)和白细胞介素-8(IL-8)的分泌,以及内皮细胞细胞间黏附分子-1(ICAM-1)的表达。有趣的是,LXA(4)上调了HUVECs中白细胞介素-10(IL-10)的产生。与对LXA(4)的这些抗炎和促炎症消退反应一致,我们证明LXA(4)抑制了白三烯D(4)和VEGF刺激的增殖和血管生成,这是通过HUVECs的管腔形成来确定的。我们探索了潜在的分子机制,并证明LXA(4)预处理与VEGF刺激的VEGF受体2(KDR/FLK-1)磷酸化及下游信号事件(包括磷脂酶C-γ、细胞外信号调节激酶1/2(ERK1/2)和蛋白激酶B(Akt)的激活)的减少有关。