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首页> 外文期刊>Arthritis Research >MicroRNA-125b regulates the expression of aggrecanase-1 (ADAMTS-4) in human osteoarthritic chondrocytes
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MicroRNA-125b regulates the expression of aggrecanase-1 (ADAMTS-4) in human osteoarthritic chondrocytes

机译:MicroRNA-125b调节人骨关节炎软骨细胞中软骨聚集蛋白聚糖酶-1(ADAMTS-4)的表达

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Introduction Increased expression of aggrecanase-1 (ADAMTS-4) has emerged as an important factor in osteoarthritis (OA) and other joint diseases. This study aimed to determine whether the expression of ADAMTS-4 in human chondrocytes is regulated by miRNA. Methods MiRNA targets were identified using bioinformatics. Chondrocytes were isolated from knee cartilage and treated with interleukin-1 beta (IL-1β). Gene expression was quantified using TaqMan assays and protein production was determined by immunoblotting. Luciferase reporter assay was used to verify interaction between miRNA and target messenger RNA (mRNA). Results In silico analysis predicted putative target sequence of miR-125b on ADAMTS-4. MiR-125b was expressed in both normal and OA chondrocytes, with significantly lower expression in OA chondrocytes than in normal chondrocytes. Furthermore, IL-1β-induced upregulation of ADAMTS-4 was suppressed by overexpression of miR-125b in human OA chondrocytes. In the luciferase reporter assay, mutation of the putative miR-125b binding site in the ADAMTS-4 3'UTR abrogated the suppressive effect of miR125. Conclusions Our results indicate that miR-125b plays an important role in regulating the expression of ADAMTS-4 in human chondrocytes and this identifies miR-125b as a novel therapeutic target in OA.
机译:简介聚集蛋白聚糖酶1(ADAMTS-4)表达的增加已成为骨关节炎(OA)和其他关节疾病的重要因素。这项研究旨在确定ADAMTS-4在人软骨细胞中的表达是否受miRNA调控。方法使用生物信息学鉴定MiRNA靶标。从膝盖软骨分离软骨细胞,并用白介素-1β(IL-1β)处理。使用TaqMan测定法对基因表达进行定量,并通过免疫印迹测定蛋白质产量。萤光素酶报告基因检测用于验证miRNA与目标信使RNA(mRNA)之间的相互作用。结果计算机分析预测了ADAMTS-4上miR-125b的假定靶序列。 MiR-125b在正常和OA软骨细胞中均表达,在OA软骨细胞中的表达明显低于正常软骨细胞。此外,miR-125b在人OA软骨细胞中的过表达抑制了IL-1β诱导的ADAMTS-4上调。在荧光素酶报告基因分析中,ADAMTS-4 3'UTR中假定的miR-125b结合位点的突变消除了miR125的抑制作用。结论我们的结果表明miR-125b在调节人软骨细胞中ADAMTS-4的表达中起着重要作用,这将miR-125b鉴定为OA中的新型治疗靶点。

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