Wang Jibo, Zhao Yingjie, Xin Miaomiao, Pan Lin, Wang Liqin, Yang Kun
Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.
Department of Central Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.
Exp Ther Med. 2018 Feb;15(2):2134-2139. doi: 10.3892/etm.2017.5609. Epub 2017 Dec 11.
The aim of the present study was to identify the effectiveness of lentivirus-mediated RNA interference (RNAi) targeting mouse tumor necrosis factor-α (TNF-α). RNAi lentivirus was used to transfect RAW264.7 cells, and the expression of -α, interleukin ()-β and mRNAs and TNF-α protein in RAW264.7 cells was measured by reverse transcription quantitative polymerase chain reaction (RT-qPCR) and enzyme-linked immunosorbent assay, respectively. , mice with collagen-induced arthritis (CIA) were injected intravenously with RNAi lentivirus, and CIA arthritis scores and the serum levels of TNF-α were detected. Additionally, joint tissues were subjected to pathological examination. In the cells, the expression level of -α mRNA in the RNAi lentivirus group was 0.29±0.02, which was significantly lower than that of the lentivirus negative control (0.93±0.01; t=25.4, P<0.001). In the mice, the serum TNF-α level in the RNAi lentivirus group was 249.25±11.22 ng/ml, which was significantly lower than that of the negative control group (381.86±6.28 ng/ml; P<0.05). However, no difference in α and mRNA levels was identified among the groups (t=1.00, P=0.37; t=1.22, P=0.29). The CIA arthritis score in the RNAi lentivirus group was significantly reduced compared with those in the control and negative control groups (P<0.05). Furthermore, the arthritis scores in the RNAi lentivirus and positive control groups continued to decrease for ≥2 weeks, and the serum TNF-α levels in the RNAi lentivirus and positive control groups were 31.58±2.18 and 35.21±2.25 pg/ml, which were significantly lower than those in the negative control group (46.62±3.02 pg/ml; P<0.05). Thus, targeting of the -α gene in mice via lentivirus-mediated RNAi and achieved TNF-α gene downregulation, which indicates that lentivirus-mediated RNA interference may be an effective form of gene therapy against rheumatoid arthritis.
本研究的目的是确定慢病毒介导的RNA干扰(RNAi)靶向小鼠肿瘤坏死因子-α(TNF-α)的有效性。使用RNAi慢病毒转染RAW264.7细胞,分别通过逆转录定量聚合酶链反应(RT-qPCR)和酶联免疫吸附测定法检测RAW264.7细胞中TNF-α、白细胞介素(IL)-β和mRNA的表达以及TNF-α蛋白。此外,将胶原诱导性关节炎(CIA)小鼠静脉注射RNAi慢病毒,检测CIA关节炎评分和TNF-α的血清水平。另外,对关节组织进行病理检查。在细胞中,RNAi慢病毒组中TNF-α mRNA的表达水平为0.29±0.02,显著低于慢病毒阴性对照组(0.93±0.01;t=25.4,P<0.001)。在小鼠中,RNAi慢病毒组的血清TNF-α水平为249.25±11.22 ng/ml,显著低于阴性对照组(381.86±6.28 ng/ml;P<0.05)。然而,各组之间α和mRNA水平未发现差异(t=1.00,P=0.37;t=1.22,P=0.29)。与对照组和阴性对照组相比,RNAi慢病毒组的CIA关节炎评分显著降低(P<0.05)。此外,RNAi慢病毒组和阳性对照组的关节炎评分持续下降≥2周,RNAi慢病毒组和阳性对照组的血清TNF-α水平分别为31.58±2.18和35.21±2.25 pg/ml,显著低于阴性对照组(46.62±3.02 pg/ml;P<0.05)。因此,通过慢病毒介导的RNAi靶向小鼠中的TNF-α基因可实现TNF-α基因下调,这表明慢病毒介导的RNA干扰可能是一种针对类风湿性关节炎的有效基因治疗形式。