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首页> 外文期刊>Inflammatory bowel diseases >Effect of Long Noncoding RNA H19 Overexpression on Intestinal Barrier Function and Its Potential Role in the Pathogenesis of Ulcerative Colitis
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Effect of Long Noncoding RNA H19 Overexpression on Intestinal Barrier Function and Its Potential Role in the Pathogenesis of Ulcerative Colitis

机译:长期非编码RNA H19过表达对溃疡性结肠炎肠道屏障功能的影响及其在发病机制中的潜在作用

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Background:Recently, long noncoding RNA (lncRNA) H19 has been reported to be related with VDR signaling and the development of inflammatory diseases including osteoarthritis. The aim of this study was to investigate the correlation between the expression level of H19 and VDR in ulcerative colitis (UC) tissues and to investigate the effect of H19 overexpression on intestinal epithelial barrier function.Methods:The expression level of H19, miR-675-5p, and VDR in UC tissues and paired normal tissues collected from 12 patients with UC was investigated by quantitative real-time polymerase chain reaction. Caco-2 monolayers were used to test the effect of H19 and miR-675-5p overexpression on the intestinal epithelial barrier function and the status of tight junction proteins and VDR. Luciferase assay was used to validate the target site of miR-675-5p in the 3UTR of VDR mRNA.Results:The expression of H19 was found to be negatively correlated with the expression of VDR in UC tissues (r = 0.5369, P < 0.05). The expression of miR-675-5p was also found to be negatively correlated with the expression of VDR in UC tissues (r = 0.5233, P < 0.01). H19 overexpression increased Caco-2 monolayer permeability and decreased the expression of tight junction proteins and VDR, which was significantly attenuated by cotransfection with miR-675-5p inhibitors. The 3'UTR of VDR mRNA was validated to be one of the direct targets of miR-675-5p.Conclusions:This study reveals the destructive effect of H19 overexpression on intestinal epithelial barrier function and suggests a potential role of H19 in the development of UC. In addition, H19 overexpression may be one of the mechanisms underlying the decreased expression of VDR in UC tissues and the interaction between H19 and VDR signaling may provide potential therapeutic targets for UC.
机译:背景:最近,据报道,长非编码RNA(IncRNA)H19与VDR信号传导和包括骨关节炎在内的炎性疾病的发展有关。本研究旨在探讨溃疡性结肠炎(UC)组织中H19和VDR表达水平之间的相关性,并探讨H19过表达对肠上皮屏障功能的影响。方法:H19,miR-675的表达水平通过定量实时聚合酶链反应研究了从12例UC患者中收集的UC组织和配对的正常组织中的-5p和VDR。 Caco-2单层膜用于测试H19和miR-675-5p过表达对肠上皮屏障功能以及紧密连接蛋白和VDR状态的影响。用荧光素酶法验证了VDR mRNA 3UTR中miR-675-5p的靶位点。结果:发现H19的表达与UC组织中VDR的表达呈负相关(r = 0.5369,P <0.05 )。还发现miR-675-5p的表达与UC组织中VDR的表达呈负相关(r = 0.5233,P <0.01)。 H19过表达增加了Caco-2单层通透性,并降低了紧密连接蛋白和VDR的表达,这与miR-675-5p抑制剂共转染可显着减弱。结论:VDR mRNA的3'UTR是miR-675-5p的直接靶标之一。 UC。另外,H19过表达可能是UC组织中VDR表达降低的潜在机制之一,并且H19和VDR信号之间的相互作用可能为UC提供潜在的治疗靶标。

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