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作 者:刘媛[1] 王文博[2] 邹自英[1] 朱冰[1] 弓超[2] 曹雪峰[2] 胡宗海[1] 熊杰[1]
机构地区:[1]成都军区总医院检验科,成都610083 [2]成都军区疾病预防控制中心,成都610021
出 处:《重庆医科大学学报》2017年第11期1488-1493,共6页Journal of Chongqing Medical University
基 金:国家自然科学基金资助项目(编号:81301445);院管课题基金资助项目(编号:2013YG-B055)
摘 要:目的:探索TNF-α抑制剂对丙型肝炎病毒感染肝细胞的影响。方法:体外培养肝癌细胞株Huh7细胞,分为未处理组、NFκB抑制剂[6-amino-4-(4-phenoxyphenylethylamino)quinazoline,QNZ]处理组、咖啡酸苯乙酯(caffeic acid phenethyl ester,CAPE)处理组和TNF-α抑制剂来那度胺(Lenalidomide)处理组,每组设置浓度梯度为100μmol/L至1.28 nmol/L,5倍倍比稀释,通过CCK8法检测各抑制剂对细胞增殖的影响;Huh7细胞经抑制剂处理后,再以丙型肝炎病毒感染,通过荧光定量PCR和免疫荧光法检测细胞内病毒的感染水平。结果:100μmol/L QNZ处理组(0.730±0.056)和100μmol/L CAPE处理组(1.040±0.014)细胞在450 nm处的吸光度(absorbance,A)值均低于未处理组(1.190±0.040,P=0.000)。Lenalidomide各浓度处理组(100μmol/L处理组,1.250±0.016)细胞增殖水平与未处理组相当(P=0.306)。在抗病毒活性方面,100 nmol/L Lenalidomide处理组[(3.79±0.88)×105]和QNZ处理组[(6.64±1.11)×105]HCV RNA水平明显低于未处理组[(1.51±0.45)×10~6,P=0.000],而CAPE处理组[(1.61±0.15)×10~6]与未处理组HCV RNA水平相当(P=0.383)。结论:TNF-α抑制剂Lenalidomide对细胞毒性较小,能够在细胞水平上抑制丙型肝炎病毒的感染。Objective:To research the effect of TNF-α inhibitors on hepatitis C virus(HCV) infection in hepatocytes. Methods:Hep- atoma Huh7 cells were cultured in vitro. Huh7 cells divided into four groups:untreated group,NFKB inhibitors [6-amino-4-(4-phe- noxyphenylethylamino) quinazoline, QNZ] treated group,caffeic acid phenethyl ester (CAPE)) treated group and TNF-α inhibitors (Lenalidomide) treated group. Concentrations of the inhibitors were from 100 μmol/L to 1.28 nmol/L with 5-fold serial dilution in each group. Cell proliferation was observed via CCK8 methods. Huh7 cells pre-treated with inhibitors were followed with HCV infection. The intracellular HCV RNA and protein levels were determined by quantitative PCR and immunofluorescence assay. Results:The ab- sorbance values at 450 nm of 100 μmol/L QNZ treatment group(0.730 ± 0.056) and 100 μmol/L CAPE treatment group(1.040 ± 0.014) were lower than those of untreated group(1.190 ± 0.040,P=0.000). The proliferation level of each concentration of Lenalido- mide treatment group(100 μmol/L treatment group, 1.250± 0.016) was similar with untreated group(P=0.306). In terms of antiviral activity,the HCV RNA levels of 100 nmol/L Lenalidomide treatment group[(3.79 ± 0.88) × 10^5] and QNZ treatment group[(6.64 ± 1.11 ) ×10^5] were significantly lower than those of untreated group[( 1.51± 0.45) × 10^6, P=0.000]. CAPE treatment group[( 1.61 ± 0.15) ×10^6] had a similar HCV RNA level with untreated group(P=0.383). Conclusion :TNF-α inhibitor Lenalidomide is less toxic to cells and can inhibit hepatitis C virus infection in hepatocytes.
关 键 词:丙型肝炎病毒 TNF-α抑制剂:抗病毒活性
分 类 号:R373.2[医药卫生—病原生物学]
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