The retinoic acid receptor-related orphan receptor &agr; positively regulates tight junction protein claudin domain-containing 1 mRNA expression in human brain endothelial cells

H. Matsuoka, Akiho Shima, A. Uda, Hirotaka Ezaki, A. Michihara
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引用次数: 8

Abstract

Members of the claudin family play important roles in the formation of tight junctions (TJs) in several tissues. Claudin domain containing 1 (CLDND1) is homologous to this family and localizes to TJs and the cytoplasm when exogenously expressed in cultured epithelial cell lines. Furthermore, serum antibody levels of CLDND1-derived peptides are elevated in patients with cerebral infection, cardiovascular disease or diabetes mellitus as compared to healthy controls. However, CLDND1 transcriptional regulation remains poorly analyzed and most regional transcription factor binding sites remain to be defined. Notably, the CLDND1 promoter contains a putative response element for retinoic acid receptor-related orphan receptor α (RORα), which is involved in the above-mentioned disorders. In this study, we found that Cldnd1 and Rora mRNA levels are correlated in rat tissues and that RORα overexpression in human brain endothelial cells enhanced CLDND1 transcript expression. In addition, siRNA-mediated knockdown of RORα significantly decreased CLDND1 transcription. An electrophoresis mobility shift assay indicated that RORα binds to the identified response element in a sequence-specific manner. Furthermore, luciferase reporter assays confirmed that RORα interacts with the CLDND1 promoter to enhance transcription. Taken together, our findings strongly suggest that CLDND1 is a direct RORα target.
视黄酸受体相关孤儿受体;正调控人脑内皮细胞紧密连接蛋白含claudin结构域1mrna的表达
claudin家族的成员在许多组织的紧密连接(TJs)的形成中发挥重要作用。Claudin domain containing 1 (CLDND1)与该家族同源,在培养的上皮细胞系外源表达时定位于TJs和细胞质。此外,与健康对照组相比,脑感染、心血管疾病或糖尿病患者的血清cldnd1衍生肽抗体水平升高。然而,对CLDND1转录调控的分析仍然很少,大多数区域转录因子结合位点仍有待确定。值得注意的是,CLDND1启动子含有维甲酸受体相关孤儿受体α (RORα)的推定应答元件,该元件参与上述疾病。在本研究中,我们发现Cldnd1和Rora mRNA水平在大鼠组织中是相关的,并且在人脑内皮细胞中Rora过表达增强了Cldnd1转录物的表达。此外,sirna介导的rora敲低可显著降低CLDND1的转录。电泳迁移率转移分析表明,rora以序列特异性的方式与鉴定的响应元件结合。此外,荧光素酶报告基因检测证实,rora与CLDND1启动子相互作用以增强转录。综上所述,我们的研究结果强烈表明CLDND1是rora的直接靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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