Oskolkova Olga, Gawlak Grzegorz, Tian Yufeng, Ke Yunbo, Sarich Nicolene, Son Sophia, Andreasson Katrin, Bochkov Valery N, Birukova Anna A, Birukov Konstantin G
Lung Injury Center, Section of Pulmonary and Critical Medicine, Department of Medicine, University of Chicago, Chicago, Illinois, USA.
Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
FASEB J. 2017 Sep;31(9):4187-4202. doi: 10.1096/fj.201601232RR. Epub 2017 Jun 1.
Unlike other agonists that cause transient endothelial cell (EC) response, the products of 1-palmitoyl-2-arachidonoyl--glycero-3-phosphocholine (PAPC) oxidation that contain cyclopenthenone groups, which recapitulate prostaglandin-like structure, cause sustained enhancement of the pulmonary EC barrier. The mechanisms that drive the sustained effects by oxidized PAPC (OxPAPC) remain unexplored. On the basis of the structural similarity of isoprostanoid moieties that are present in full-length oxygenated PAPC species, we used an inhibitory approach to perform the screening of prostanoid receptors as potential candidates that mediate OxPAPC effects. Results show that only prostaglandin E receptor-4 (EP4) was involved and mediated the sustained phase of the barrier-enhancing effects of OxPAPC that are associated with the activation of Rac GTPase and its cytoskeletal targets. EC incubation with OxPAPC also induced EP4 mRNA expression in pulmonary ECs and lung tissue. EP4 knockdown using gene-specific small interfering RNA did not affect the rapid phase of OxPAPC-induced EC barrier enhancement or the protective effects against thrombin-induced EC permeability, but abolished the advanced barrier enhancement phase and suppressed the protective effects of OxPAPC against more sustained EC barrier dysfunction and cell inflammatory response caused by TNF-α. Endothelial-specific knockout of the EP4 receptor in mice attenuated the protective effect of intravenous OxPAPC administration in the model of acute lung injury caused by intratracheal injection of LPS. Taken together, these results demonstrate a novel role for prostaglandin receptor EP4 in the mediation of barrier-enhancing and anti-inflammatory effects caused by oxidized phospholipids.-Oskolkova, O., Gawlak, G., Tian, Y., Ke, Y., Sarich, N., Son, S., Andreasson, K., Bochkov, V. N., Birukova, A. A., Birukov, K. G. Prostaglandin E receptor-4 receptor mediates endothelial barrier-enhancing and anti-inflammatory effects of oxidized phospholipids.
与其他引起内皮细胞(EC)短暂反应的激动剂不同,1-棕榈酰-2-花生四烯酰-sn-甘油-3-磷酸胆碱(PAPC)氧化产物中含有环戊烯酮基团,其结构类似前列腺素,可使肺内皮细胞屏障持续增强。氧化型PAPC(OxPAPC)产生持续效应的机制尚不清楚。基于全长氧化型PAPC物种中存在的异前列腺素部分的结构相似性,我们采用抑制性方法对前列腺素受体进行筛选,以寻找介导OxPAPC效应的潜在候选受体。结果表明,只有前列腺素E受体4(EP4)参与并介导了OxPAPC增强屏障效应的持续阶段,这与Rac GTPase及其细胞骨架靶点的激活有关。用OxPAPC孵育内皮细胞也可诱导肺内皮细胞和肺组织中EP4 mRNA表达。使用基因特异性小干扰RNA敲低EP4并不影响OxPAPC诱导的内皮细胞屏障增强的快速阶段或对凝血酶诱导的内皮细胞通透性的保护作用,但消除了晚期屏障增强阶段,并抑制了OxPAPC对由肿瘤坏死因子-α引起的更持续的内皮细胞屏障功能障碍和细胞炎症反应的保护作用。小鼠内皮细胞特异性敲除EP4受体减弱了静脉注射OxPAPC对气管内注射脂多糖引起的急性肺损伤模型的保护作用。综上所述,这些结果表明前列腺素受体EP4在介导氧化磷脂的屏障增强和抗炎作用中具有新的作用。-奥斯科尔科娃,O.,加夫拉克,G.,田,Y.,柯,Y.,萨里奇,N.,宋,S.,安德烈亚松,K.,博奇科夫,V.N.,比鲁科娃,A.A.,比鲁科夫,K.G.前列腺素E受体4介导氧化磷脂的内皮屏障增强和抗炎作用。