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首页> 外文期刊>Arthritis research & therapy. >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。这项研究旨在确定人软骨细胞中ADAMTS-4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miR-125b在ADAMTS-4上的假定靶序列。 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。在萤光素酶报告基因检测中,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的新型治疗靶点。

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