Smutny Tomas, Dusek Jan, Hyrsova Lucie, Nekvindova Jana, Horvatova Alzbeta, Micuda Stanislav, Gerbal-Chaloin Sabine, Pavek Petr
Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Kralove, Charles University, Hradec Kralove CZ-500 05, Czech Republic.
Institute of Clinical Biochemistry and Diagnostics, University Hospital Hradec Kralove, Hradec Kralove CZ-500 05, Czech Republic.
Acta Pharm Sin B. 2020 Jan;10(1):136-152. doi: 10.1016/j.apsb.2019.09.010. Epub 2019 Oct 21.
Pregnane X receptor (PXR) is the major regulator of xenobiotic metabolism. PXR itself is controlled by various signaling molecules including glucocorticoids. Moreover, negative feed-back regulation has been proposed at the transcriptional level. We examined the involvement of the 3'-untranslated region (3'-UTR) of mRNA and microRNAs in PXR- and glucocorticoid receptor (GR)-mediated regulation of gene expression. PXR ligands were found to significantly downregulate mRNA expression in a set of 14 human hepatocyte cultures. Similarly, PXR was downregulated by PCN in the C57/BL6 mice liver. In mechanistic studies with the full-length 3'-UTR cloned into luciferase reporter or expression vectors, we showed that the 3'-UTR reduces PXR expression. From the miRNAs tested, miR-18a-5p inhibited both expression and gene induction. Importantly, we observed significant upregulation of miR-18a-5p expression 6 h after treatment with the PXR ligand rifampicin, which indicates a putative mechanism underlying negative feed-back regulation in hepatic cells. Additionally, glucocorticoids upregulated expression not only through the promoter region but also 3'-UTR regulation, which likely involves downregulation of miR-18a-5p. We conclude that miR-18a-5p is involved in the down-regulation of expression by its ligands and in the upregulation of mRNA expression by glucocorticoids in hepatic cells.
孕烷X受体(PXR)是外源性物质代谢的主要调节因子。PXR自身受包括糖皮质激素在内的多种信号分子调控。此外,在转录水平已提出负反馈调节。我们研究了mRNA的3'非翻译区(3'-UTR)和微小RNA在PXR和糖皮质激素受体(GR)介导的基因表达调控中的作用。在一组14种人肝细胞培养物中,发现PXR配体可显著下调mRNA表达。同样,在C57/BL6小鼠肝脏中,PCN可下调PXR。在用克隆到荧光素酶报告基因或表达载体中的全长3'-UTR进行的机制研究中,我们表明3'-UTR可降低PXR表达。在所测试的微小RNA中,miR-18a-5p可抑制表达和基因诱导。重要的是,在用PXR配体利福平处理6小时后,我们观察到miR-18a-5p表达显著上调,这表明肝细胞中负反馈调节的一种潜在机制。此外,糖皮质激素不仅通过启动子区域上调表达,还通过3'-UTR调节,这可能涉及miR-18a-5p的下调。我们得出结论,miR-18a-5p参与其配体对表达的下调以及糖皮质激素对肝细胞中mRNA表达的上调。