Suppr超能文献

细胞因子上调人气道平滑肌细胞血管内皮生长因子的分泌:内源性前列腺素的作用

Cytokines upregulate vascular endothelial growth factor secretion by human airway smooth muscle cells: Role of endogenous prostanoids.

作者信息

Stocks Joanne, Bradbury Dawn, Corbett Lisa, Pang Linhua, Knox Alan J

机构信息

Division of Respiratory Medicine, Clinical Sciences Building, City Hospital, Nottingham, UK.

出版信息

FEBS Lett. 2005 May 9;579(12):2551-6. doi: 10.1016/j.febslet.2005.02.083. Epub 2005 Apr 7.

Abstract

Here, we report that vascular endothelial growth factor (VEGF)-A secretion by human airway smooth muscle cells was increased by interleukin 1 beta (IL-1beta) and transforming growth factor beta (TGFbeta). IL-1beta and TGFbeta induced cyclo-oxygenase (COX)-2 protein and increased prostaglandin E(2) (PGE(2)). Both IL-1beta and TGFbeta increased VEGF-A(165) mRNA and VEGF promoter luciferase construct activity, in addition VEGF-A protein was inhibited by actinomycin D suggesting transcriptional regulation. The COX inhibitors indomethacin and NS398 inhibited IL-1beta but not TGFbeta mediated VEGF-A production. Furthermore, the effect of the COX inhibitors was overcome by adding exogenous PGE(2). In conclusion, IL-1beta increases VEGF-A secretion by COX-2 derived PGE(2) production whereas TGFbeta uses COX-independent pathways.

摘要

在此,我们报告白细胞介素1β(IL-1β)和转化生长因子β(TGFβ)可增加人气道平滑肌细胞血管内皮生长因子(VEGF)-A的分泌。IL-1β和TGFβ可诱导环氧化酶(COX)-2蛋白表达并增加前列腺素E2(PGE2)。IL-1β和TGFβ均可增加VEGF-A165 mRNA和VEGF启动子荧光素酶构建体活性,此外放线菌素D可抑制VEGF-A蛋白表达,提示存在转录调控。COX抑制剂吲哚美辛和NS398可抑制IL-1β介导的VEGF-A产生,但不能抑制TGFβ介导的VEGF-A产生。此外,添加外源性PGE2可克服COX抑制剂的作用。总之,IL-1β通过COX-2衍生的PGE2产生增加VEGF-A分泌,而TGFβ则通过不依赖COX的途径发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验