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机构地区:[1]重庆医科大学附属第一医院感染科,400016 [2]重庆医科大学病毒性肝炎研究所、感染性疾病分子生物学教育部重点实验室
出 处:《中华肝脏病杂志》2009年第8期615-619,共5页Chinese Journal of Hepatology
基 金:国家自然科学基金(30671866)
摘 要:目的观察超级白细胞介素-6重组慢病毒对人正常肝细胞L—02的促增殖作用。方法利用慢病毒表达质粒及其包装系统构建超级白细胞介素-6重组慢病毒(FIV—Hyper—IL-6)、IL-6重组慢病毒(FIV-IL-6)和空慢病毒载体(FIV),用嘌呤霉素筛选的方法测定其病毒滴度。将人肝细胞L02分为4组:FIV-Hyper—IL-6组、FIV-IL-6组、FIV组及未感染组,各组分别感染其相应的重组慢病毒,采用四甲基偶氮唑盐法检测其对L-02细胞生长状态的影响;并用RT—PCR法检测重组慢病毒感染L02细胞后产生的急性时相蛋白结合珠蛋白mRNA表达量的变化。应用方差分析进行统计学分析。结果构建出的各重组慢病毒能成功感染靶细胞,嘌呤霉素筛选法测得的各重组慢病毒的病毒滴度均为10^3pfu/ml。病毒颗粒感染L02细胞后48h,细胞的促增殖作用(4值)FIV—Hyper—IL-6组为0.6267±0.0256,FIV—IL-6组、FIV组及未感染组分别为0.5563±0.0112、0.5040±0.0078、0.4790±0.0201,F=41.09,P值均〈0.01,且随着时间的延长,对细胞的促增殖作用有所增加,并于感染后72h达到最高,为0.8000±0.0166。FIV—Hyper—IL-6组细胞结合珠蛋白mRNA吸光度值为0.7030±0.0106,FIV—IL-6组、FIV组及未感染组分别为0.3355±0.0093、0.1143±0.0153、0.1145±0.0076,q=57.5007,P值均〈0.01。结论构建的Hyper-IL-6重组慢病毒能够显著刺激L-02细胞表达结合珠蛋白,对L-02细胞有较强的促增殖作用。Objective To investigate the effect of Hyper-IL-6 on the proliferation of L-02 cells. Methods The recombinant lentiviral vectors encoding Hyper-IL-6 (FIV-Hyper-IL-6), IL-6 (FIV-IL-6) and the lentiviral (FIV) were prepared using the FIV-based lentiviral vectors and the packaging system. The titer of FIV-Hyper-IL-6, FIV-IL-6 and FIV was tested with puromycin. L-02 cells were infected with FIV-Hyper- IL-6, FIV-IL-6, FIV, or mock-infected. The growth rate of L02 cells was analyzed with MTT at different time points after infection. The changes of Haptoglobin in L-02 cells were analyzed with RT-PCR. Results FIV- Hyper-IL-6, FIV-IL-6 and FIV were successfully constructed, and the titer was 107 pfu/ml. 48 hours after infection, the absorbance of the cells infected with FIV-Hyper-IL-6 was 0.6267 ± 0.0256, and the absorbances of FIV-IL-6 infected cells, FIV infected cells and mock-infected cells were 0.5563 ±0.0112, 0.5040 ± 0.0078 and 0.4790 ±0.0201, respectively. There were significant differences between the FIV-Hyper-IL-6 group and the other groups (F = 41.09, P 〈 0.01). The ratio of the absorbance between haptoglobin mRNA and beta-actin was 0.7030 ± 0.0106, 0.3355 ± 0.0093, 0.1145± 0.0076 and 0.1143 ±0.0153, respectively,in FIV-Hyper-IL-6 infected cells, FIV-IL-6 infected cells, FIV infected cells and mock-infected cells. There were significant differences between the FIV-Hyper-IL-6 group and the others (q = 57.5007, P 〈 0.01). Condusion Compared with IL-6, Hyper-IL-6 is more potent to stimulate proliferation and induce the expression of Haptoglobin in L-02 cells.
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