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骨桥蛋白抑制骨关节炎软骨细胞中HIF-2α mRNA的表达。

Osteopontin inhibits HIF-2α mRNA expression in osteoarthritic chondrocytes.

作者信息

Cheng Chao, Zhang Fang-Jie, Tian Jian, Tu Min, Xiong Yi-Lin, Luo Wei, Li Yu-Sheng, Song Bing-Bing, Gao Shu-Guang, Lei Guang-Hua

机构信息

Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, P.R. China.

Hunan Province Environmental Monitoring Center, Changsha, Hunan 410019, P.R. China.

出版信息

Exp Ther Med. 2015 Jun;9(6):2415-2419. doi: 10.3892/etm.2015.2434. Epub 2015 Apr 20.

DOI:10.3892/etm.2015.2434
PMID:26136997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4473661/
Abstract

The aim of the present study was to investigate the effect of osteopontin (OPN) on the expression of hypoxia-inducible factor-2α (HIF-2α) in chondrocytes and the role of OPN in osteoarthritis (OA). Cartilage was purified from the tibial surfaces of patients with OA of the knee and cultured to obtain chondrocytes. Recombinant human OPN (rhOPN) and OPN small interfering RNA (siRNA) were used to treat the chondrocytes, and the changes in the expression levels of the HIF-2α gene were measured. An anti-CD44 blocking monoclonal antibody (mAb) was used to determine the probable ligand-receptor interactions. Reverse transcription-quantitative polymerase chain reaction assays were designed and validated with SYBR® Green dyes for the simultaneous quantification of the mRNA expression levels of OPN and HIF-2α. The mRNA expression level of HIF-2α was markedly decreased in the rhOPN-treated group compared with that in the control group; by contrast, OPN siRNA increased HIF-2α gene expression. CD44 blocking mAb suppressed the inhibitory effect of OPN on HIF-2α mRNA expression. The results of the present study suggest that OPN may play a protective role in OA by inhibiting HIF-2α gene expression in osteoarthritic chondrocytes through CD44 interaction.

摘要

本研究的目的是探讨骨桥蛋白(OPN)对软骨细胞中缺氧诱导因子-2α(HIF-2α)表达的影响以及OPN在骨关节炎(OA)中的作用。从膝骨关节炎患者的胫骨表面纯化软骨并进行培养以获得软骨细胞。使用重组人OPN(rhOPN)和OPN小干扰RNA(siRNA)处理软骨细胞,并检测HIF-2α基因表达水平的变化。使用抗CD44阻断单克隆抗体(mAb)来确定可能的配体-受体相互作用。设计并使用SYBR® Green染料验证逆转录-定量聚合酶链反应分析,以同时定量OPN和HIF-2α的mRNA表达水平。与对照组相比,rhOPN处理组中HIF-2α的mRNA表达水平明显降低;相反,OPN siRNA增加了HIF-2α基因表达。CD44阻断mAb抑制了OPN对HIF-2α mRNA表达的抑制作用。本研究结果表明,OPN可能通过与CD44相互作用抑制骨关节炎软骨细胞中的HIF-2α基因表达,从而在OA中发挥保护作用。

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