Xue Yan-Yan, Liu Hui-Jie, Sun Zhan-Juan, Xiang Ting, Shao Ping
Department of Rheumatology and Immunology, First People's Hospital of Lianyungang, No. 6 Zhenhuadong Road, Lianyungang, 222002, Jiangsu, China.
Immunol Res. 2022 Jun;70(3):392-399. doi: 10.1007/s12026-022-09276-x. Epub 2022 Mar 21.
A great number of studies have confirmed that long noncoding RNA (lncRNA) are involved in the regulation of inflammatory response in acute gouty arthritis (AGA). This paper aimed to survey the regulatory mechanism of H19 on AGA. The expression of serum H19 in all subjects was examined by qRT-PCR. The ROC curve was used to estimate the diagnostic value of H19 for AGA. THP-1 cells were induced by MSU to establish in vitro AGA cell model. The concentrations of cytokines such as IL-1β, IL-8, and TNF-α were tested by ELISA. Luciferase reporter gene analysis was used to verify the interaction between H19 and the 3'-UTR of miR-22-3p. Expressions of serum H19 in AGA patients were significantly higher than that in controls. The ROC curve indicated the potential of H19 as a diagnostic marker for AGA. Cell experiments revealed that the downregulation of H19 significantly inhibited the expressions of IL-1β, IL-8, and TNF-α. The luciferase reporter gene assay manifested that miR-22-3p is the target gene of H19. And knockdown of miR-22-3p overturned the downregulation of inflammatory factors caused by H19 inhibition. H19 aggravated MSU-induced THP-1 inflammation by negatively targeting miR-22-3p, suggesting a new regulatory mechanism and potential therapeutic target for AGA.
大量研究证实,长链非编码RNA(lncRNA)参与急性痛风性关节炎(AGA)炎症反应的调控。本文旨在探究H19对AGA的调控机制。采用qRT-PCR检测所有受试者血清H19的表达。利用ROC曲线评估H19对AGA的诊断价值。用MSU诱导THP-1细胞建立体外AGA细胞模型。通过ELISA检测IL-1β、IL-8和TNF-α等细胞因子的浓度。采用荧光素酶报告基因分析验证H19与miR-22-3p的3'-UTR之间的相互作用。AGA患者血清H19表达明显高于对照组。ROC曲线表明H19具有作为AGA诊断标志物的潜力。细胞实验显示,H19的下调显著抑制IL-1β、IL-8和TNF-α的表达。荧光素酶报告基因检测表明miR-22-3p是H19的靶基因。敲低miR-22-3p可逆转H19抑制引起的炎症因子下调。H19通过负向靶向miR-22-3p加重MSU诱导的THP-1炎症,提示了一种新的AGA调控机制和潜在治疗靶点。