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小干扰RNA有效抑制乙型肝炎病毒的动物实验
引用本文:应若素,范学工,朱才,李宁,田雪飞. 小干扰RNA有效抑制乙型肝炎病毒的动物实验[J]. 中华传染病杂志, 2006, 24(4): 239-242
作者姓名:应若素  范学工  朱才  李宁  田雪飞
作者单位:1. 广州市第八人民医院
2. 410008,长沙,中南大学湘雅医院感染病科
基金项目:湖南省科技厅重点项目(05sk2001)
摘    要:目的 以乙型肝炎病毒(HBV)S区为靶位,观察小干扰RNA(siRNA)在动物体内抗HBV的效果。方法 以流体动力学法建立HBV感染的动物模型,将pcDNA3.1-HBV和细胞体外实验证明有效的siRNA尾静脉共注射Balb/c小鼠,用时间分辨免疫荧光分析法(IFMA)检测小鼠血清中HBsAg,用定量聚合酶链反应法(FQ-PCR)检测血清HBV DNA,用逆转录聚合酶链反应(RT-PCR)法检测HBV S-mRNA,用免疫组织化学法检测肝组织HBsAg和HBcAg。结果 在小鼠体内,siRNA能有效抑制HBsAg的分泌,降低HBVDNA的滴度,免疫组织化学结果也证实HBsAg、HBcAg刚性细胞数明显减少,干扰效果至少持续3d,而无关siRNA则无抑制作用。结论 在动物体内靶向HBV S区的siRNA能有效特异抑制HBV。

关 键 词:RNA  小分子干扰 肝炎病毒  乙型 动力学 疾病模型  动物
收稿时间:2005-07-24
修稿时间:2005-07-24

Inhibition of Hepatitis B virus replication by small interfering RNA in vivo
YING Ruo-su, FAN Xue-gong, ZHU Cai,et al.. Inhibition of Hepatitis B virus replication by small interfering RNA in vivo[J]. Chinese Journal of Infectious Diseases, 2006, 24(4): 239-242
Authors:YING Ruo-su   FAN Xue-gong   ZHU Cai  et al.
Affiliation:Department of Infectious Diseases, Xiangya Hospital, Central South Universify, Changsha 410008, China
Abstract:Objective To evaluate the inhibitory effect of the small interfering RNA(siRNA) on hepatitis B virus(HBV)in vivo which targets HBV S gene region.Methods An animal model of HBV infection was developed hydrodynamically by injecting pcDNA3.1-HBV together with siRNA through the tail vein of Balb/c.HBsAg was analyzed by time resolved immunofluorometric assay, HBV DNA was analyzed by fluorogenic quantitative PCR(FQ-PCR),HBV S-mRNA was detected by semi-quantitative RT-PCR,and viral specific proteins(HBsAg and HBcAg)in the liver were assayed by immunohistochemical staining.Results In the mice,the siRNA could effectively inhibit the secre- tion of HBsAg,reduce the titers of HBV DNA,and immunohistochemical results also indicated that the number of HBsAg and HBcAg positive cells was reduced.The inhibitory effect of siRNA on HBV lasted 3 clays at least.Conclusion These results demonstrate that the siRNA targeting HBV S gene region can substantially and specifically inhibit HBV replication and expression in vivo.
Keywords:RNA, small interfering   Hepatitis B virus   Kinetics   Disease models, animal
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