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沉默环氧化酶-2(COX-2)/聚集蛋白水解酶-1 与过表达胰岛素样生长因子 1(IGF-1)在骨关节炎动物模型中的交叉偶联作用。

Cross-Coupling Effects of Silencing of Cyclooxygenase-2 (COX-2)/Aggrecanase-1 and Over-Expressed Insulin-Like Growth Factor 1 (IGF-1) in an Osteoarthritis Animal Model.

机构信息

Department of Hand and Foot Surgery, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).

Department of Joint Surgery, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).

出版信息

Med Sci Monit. 2017 Nov 7;23:5302-5310. doi: 10.12659/msm.907150.

Abstract

BACKGROUND This study aimed to observe the effect of lentivirus-mediated cyclooxygenase-2 and aggrecanase-1 silencing and insulin-like growth factor-1 overexpression in human bone marrow mesenchymal stem cells after injection into model osteoarthritic knees. MATERIAL AND METHODS Using genetic recombination technique, the genes of cyclooxygenase-2, aggrecanase-1, and insulin-like growth factor-1 were recombined into the lentiviral vectors, and we transfected the human bone marrow stem cells in vitro. The BMSC transfected with lentivirus without genes served as a blank-virus group, and saline was used for another control group. One week later, the cytokines PGE2, aggrecanase-1, hIGF-1, and IL-1 were detected and compared between groups. RESULTS Compared with blank-virus group, the expression of COX-2 (85.81±5.12 ng/L) and aggrecanase1 (6.256±1.66) were decreased in the virus group (p<0.05), while the expression of hIGF-1 (17.46±1.86) was increased (p<0.05). The concentrations of PGE2 (85.81±5.12 ng/L), aggrecanase1 (51.34±5.463 ng/L), and IL-1 (82.31±4.321 ng/L) decreased (p<0.05) within the knee, but the concentration of hIGF-1 (44.33±0.7194 ng/L) increased (p<0.05). Compared with the other groups, the results of histological and immunohistochemical examinations demonstrated that the abrasion of articular cartilage was significantly improved and repaired. CONCLUSIONS Lentivirus-mediated RNAi can inhibit the expression of COX-2 mRNA and aggrecanase-1mRNA, and enhance the hIGF-1 mRNA expression, thereby influencing the concentration of cytokines in the early osteoarthritic model knee joints.

摘要

背景

本研究旨在观察慢病毒介导的环氧合酶-2 和聚集蛋白水解酶-1 沉默以及胰岛素样生长因子-1 过表达对注射到模型骨关节炎膝关节中的人骨髓间充质干细胞的影响。

材料与方法

采用基因重组技术,将环氧合酶-2、聚集蛋白水解酶-1 和胰岛素样生长因子-1 的基因重组到慢病毒载体中,并在体外转染人骨髓间充质干细胞。转染无基因慢病毒的 BMSC 作为空白病毒组,另设生理盐水对照组。1 周后,检测并比较各组细胞因子 PGE2、聚集蛋白水解酶-1、hIGF-1 和 IL-1 的表达情况。

结果

与空白病毒组相比,病毒组 COX-2(85.81±5.12ng/L)和聚集蛋白水解酶 1(6.256±1.66)的表达降低(p<0.05),hIGF-1(17.46±1.86)的表达增加(p<0.05)。膝关节内 PGE2(85.81±5.12ng/L)、聚集蛋白水解酶 1(51.34±5.463ng/L)和 IL-1(82.31±4.321ng/L)浓度降低(p<0.05),hIGF-1(44.33±0.7194ng/L)浓度增加(p<0.05)。与其他组相比,组织学和免疫组织化学检查结果表明,关节软骨的磨损明显改善和修复。

结论

慢病毒介导的 RNAi 可以抑制 COX-2mRNA 和聚集蛋白水解酶-1mRNA 的表达,增强 hIGF-1mRNA 的表达,从而影响早期骨关节炎模型膝关节细胞因子的浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cb8/5687117/5a2e400e58c9/medscimonit-23-5302-g001.jpg

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