摘要
目的筛选针对HPV16 E7基因有效的siRNA,探讨其对HaCaT-E7细胞中HPV16 E7 mRNA及细胞表面HLA-Ⅰ类分子表达的影响。方法采用化学法合成3条HPV16 E7特异性siRNA,应用转染试剂Lipofectamine2000将其转染入HaCaT-E7细胞,采用实时荧光定量PCR(RT-PCR)检测HPV16 E7 mRNA的表达,采用流式细胞术(FCM)检测细胞表面HLA-Ⅰ类分子的表达。结果3条siRNA均能有效抑制HaCaT-E7细胞中HPV16 E7的转录表达,以siR-NA2作用效果最明显,抑制率达75%,细胞膜表面HLA-Ⅰ类分子的表达明显上调,平均荧光强度(MFI)为130.18±1.07,高于空转染对照组(100.32±3.01)和非特异性siRNA对照组(100.82±2.87)。结论化学合成的HPV16 E7特异性siRNA能有效抑制HaCaT-E7细胞中E7 mRNA的表达,同时使细胞表面HLA-Ⅰ类分子表达上调。
Objective To screen an effective HPV16 E7 specific siRNA and investigate its effect on expression of HPV16 E7 mRNA and cell surface HLA class I antigen in HaCaT-E7 cells.Methods Three HPV16 E7 specific siRNAs were chemically synthesized and transfected into HaCaT-E7 cells by Lipofectamine2000.Expression of HPV16 E7 mRNA was determined by real-time PCR while expression of cell surface HLA class I antigen was determined by flow cytometry(FCM).Results All three siRNAs effectively inhibited expression of HPV16 E7 mRNA in HaCaT-E7 cells.Of the siRNAs,siRNA2 was the most effective and its inhibitory rate reached 75%.Expression of cell surface HLA class I antigen was obviously up-regulated.Post-transfected average mean fluorescence intensity(MFI) of HaCaT-E7 cell surface HLA class I antigen was 130.18±1.07,which was significantly higher than that in the mock control group(100.32±3.01) and the non-specific siRNA control group(100.82±2.87).Conclusion HPV16 E7 specific siRNA can effectively inhibit expression of E7 mRNA in HaCaT-E7 cells and induces up-regulation of cell surface HLA class I antigen.
出处
《山东大学学报(医学版)》
CAS
北大核心
2009年第11期64-67,共4页
Journal of Shandong University:Health Sciences
基金
国家自然科学基金资助项目(30672010)