Suppr超能文献

皮质酮通过调节滑膜成纤维细胞的11β-羟基类固醇脱氢酶1(11β-HSD1)生物活性来抑制白细胞介素-1β(IL-1β)诱导的巨噬细胞前列腺素E2(mPGE2)表达。

Corticosterone suppresses IL-1β-induced mPGE2 expression through regulation of the 11β-HSD1 bioactivity of synovial fibroblasts .

作者信息

Wei Bo, Zhu Zhaobo, Xiang Min, Song Lijun, Guo Weixiong, Lin Hao, Li Guangsheng, Zeng Rong

机构信息

Orthopedic Centre, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong 524001, P.R. China.

Reproductive Research Department, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong 524001, P.R. China.

出版信息

Exp Ther Med. 2017 May;13(5):2161-2168. doi: 10.3892/etm.2017.4238. Epub 2017 Mar 20.

Abstract

The aim of the present study was to investigate the correlation between glucocorticoid activity regulation, prostaglandin E2 (PGE) synthesis, and synovial inflammation inhibition activity, through microsomal prostaglandin E synthase-1 (mPGES-1) expression regulated by the glucocorticoid pre-receptor regulator, 11β-hydroxysteroid dehydrogenase-1 (11β-HSD1). In the present study, fibroblast-like synovial cells of rats were studied as a cell model. Cells were stimulated with 10 ng/ml interleukin (IL)-1β for 24 h, and were subsequently, within the next 24 h, treated with or without 10 mmol/l corticosterone alone or with 100 nmol/l PF915275. At the end of the second 24 h, PGE levels in culture supernatants were assayed. Cells were harvested for mRNA evaluation of 11β-HSD1, mPGES-1, IL-1β and tumor necrosis factor (TNF)-α, and protein detection of 11β-HSD1 and mPGES-1 using reverse transcription-qualitative polymerase chain reaction and western blot analysis, respectively. Corticosterone was demonstrated to suppress the mRNA expression levels of inflammatory factors, such as TNF-α and PGE, induced by IL-1β . Simultaneously, expression levels of 11β-HSD1 decreased significantly at the mRNA and protein levels (P<0.05). Cortisol concentration in the medium of the group treated with corticosterone was significantly increased (P<0.05) compared with that of the control group; however, the cortisol concentration was decreased in the medium when the conversion bioactivity of 11β-HSD1 was inhibited by PF915275, while the changes in 11β-HSD1 and mPGES-1 mRNA expression levels and PGE content were reversed in the medium. These results indicated that a significant positive correlation (P<0.01) may exist between mRNA and protein expression levels. To conclude, 11β-HSD1 is a key regulator for the synthesis of mPGES-1 and PGE in the inflammatory synovial cells , suggesting a potential interference target for osteoarthritis.

摘要

本研究旨在通过糖皮质激素前受体调节剂11β-羟基类固醇脱氢酶-1(11β-HSD1)调控的微粒体前列腺素E合酶-1(mPGES-1)表达,研究糖皮质激素活性调节、前列腺素E2(PGE)合成与滑膜炎症抑制活性之间的相关性。在本研究中,以大鼠成纤维样滑膜细胞作为细胞模型。细胞用10 ng/ml白细胞介素(IL)-1β刺激24小时,随后在接下来的24小时内,单独用10 mmol/l皮质酮或与100 nmol/l PF915275一起处理或不处理。在第二个24小时结束时,测定培养上清液中的PGE水平。收集细胞用于11β-HSD1、mPGES-1、IL-1β和肿瘤坏死因子(TNF)-α的mRNA评估,以及分别使用逆转录-定性聚合酶链反应和蛋白质印迹分析检测11β-HSD1和mPGES-1的蛋白质。结果表明,皮质酮可抑制IL-1β诱导的炎症因子如TNF-α和PGE的mRNA表达水平。同时,11β-HSD1的mRNA和蛋白质水平表达显著降低(P<0.05)。与对照组相比,皮质酮处理组培养基中的皮质醇浓度显著升高(P<0.05);然而,当PF915275抑制11β-HSD1的转化生物活性时,培养基中的皮质醇浓度降低,而培养基中11β-HSD1和mPGES-1 mRNA表达水平及PGE含量的变化则被逆转。这些结果表明mRNA和蛋白质表达水平之间可能存在显著正相关(P<0.01)。总之,11β-HSD1是炎症滑膜细胞中mPGES-1和PGE合成的关键调节因子提示其可能是骨关节炎的潜在干预靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10e6/5443184/1fb4bec4ff4c/etm-13-05-2161-g00.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验