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前列腺素 E2 通过培养的人肺成纤维细胞中的 E-前列腺素-2 受体刺激血管内皮生长因子的产生。

Prostaglandin E2 stimulates the production of vascular endothelial growth factor through the E-prostanoid-2 receptor in cultured human lung fibroblasts.

机构信息

Division of Pulmonary, Critical Care, Sleep and Allergy Medicine, University of Nebraska Medical Center, Nebraska Medical Center, Omaha, NE 68198-5910, USA.

出版信息

Am J Respir Cell Mol Biol. 2012 Feb;46(2):217-23. doi: 10.1165/rcmb.2010-0115OC.

Abstract

Fibroblasts are the major mesenchymal cells present within the interstitium of the lung and are a major source of vascular endothelial growth factor (VEGF), which modulates the maintenance of pulmonary microvasculature. Prostaglandin E(2) (PGE(2)) acts on a set of E-prostanoid (EP) receptors that activate multiple signal transduction pathways leading to downstream responses. We investigated the modulation by PGE(2) of VEGF release by human lung fibroblasts. Human lung fibroblasts were cultured until reaching 90% confluence in tissue culture plates, after which the culture media were changed to serum-free Dulbecco's modified Eagle's medium, with or without PGE(2), and with specific agonists or antagonists for each EP receptor. After 2 days, culture media were assayed for VEGF by ELISA. The results demonstrated that PGE(2) and the EP2 agonist ONO-AE1-259-01 significantly stimulated the release of VEGF in a concentration-dependent manner. Agonists for other EP receptors did not stimulate the release of VEGF. The stimulatory effect of PGE(2) was blocked by the EP2 antagonist AH6809, but was not blocked by antagonists for other EP receptors. The protein kinase-A (PKA) inhibitor KT-5720 also blocked the stimulatory effect of PGE(2). The increased release of VEGF induced by PGE(2) was accompanied by a transient increase in the concentration of VEGF mRNA. These findings demonstrate that PGE(2) can modulate the release of VEGF by human lung fibroblasts through its actions in the EP2 receptor/PKA pathway. This activity may contribute to the maintenance of pulmonary microvasculature in the alveolar wall.

摘要

成纤维细胞是肺间质中主要的间充质细胞,是血管内皮生长因子(VEGF)的主要来源,可调节肺微血管的维持。前列腺素 E2(PGE2)作用于一组 E 型前列腺素(EP)受体,激活多种信号转导途径,导致下游反应。我们研究了 PGE2 对人肺成纤维细胞 VEGF 释放的调节作用。人肺成纤维细胞在组织培养板中培养至 90%汇合后,将培养基更换为无血清的 Dulbecco 修改的 Eagle 培养基,其中含有或不含有 PGE2,以及每种 EP 受体的特异性激动剂或拮抗剂。2 天后,通过 ELISA 测定培养基中 VEGF 的含量。结果表明,PGE2 和 EP2 激动剂 ONO-AE1-259-01 以浓度依赖性方式显著刺激 VEGF 的释放。其他 EP 受体的激动剂不能刺激 VEGF 的释放。EP2 拮抗剂 AH6809 阻断了 PGE2 的刺激作用,但对其他 EP 受体的拮抗剂没有阻断作用。蛋白激酶 A(PKA)抑制剂 KT-5720 也阻断了 PGE2 的刺激作用。PGE2 诱导的 VEGF 释放增加伴随着 VEGF mRNA 浓度的短暂增加。这些发现表明,PGE2 可以通过其在 EP2 受体/PKA 途径中的作用来调节人肺成纤维细胞 VEGF 的释放。这种活性可能有助于维持肺泡壁中的肺微血管。

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