Kayhan H, Karatayli E, Turkyilmaz A R, Sahin F, Yurdaydin C, Bozdayi A M
Institute of Hepatology, Ankara University, Ankara, Turkey.
Arch Virol. 2007;152(5):871-9. doi: 10.1007/s00705-006-0918-5. Epub 2007 Jan 25.
In this study, the effect of RNAi on HBV replication was observed in a cell culture model, HepG2 2.2.15 cell line, which supports human HBV ayw replication and expression. Aim of the study was to investigate effects of shRNAs (small hairpin RNAs) targeting hepatitis B virus mRNAs on the viral replication in HepG2 2.2.15 cells. We selected three target HBV mRNA regions with different putative secondary structures to test whether the secondary structure of RNA may affect the inhibition efficacy on the target HBV RNA. Three HBV-specific siRNAs (small interfering RNA) were designed targeting X (1689-1708), Core (2229-2248) and S (765-784 nt) transcripts. HepG2 2.2.15 cells were transfected with shRNA expressing plasmids, P765, P2229 and P1689 targeting S, core and X region, respectively or a mock plasmid targeting lacZ gene. The culture media was collected throughout six days after transfection and analyzed by real-time PCR. Viral DNA production was suppressed for 7 days. The HBV DNA levels were decreased by 73, 72 and 79% with P765, P2229 and P1689 vectors, respectively. In conclusion, the shRNAs designed for X, core and S regions, specifically and significantly suppressed HBV DNA. siRNAs potentially may be used in treatment of hepatitis B.
在本研究中,在支持人乙肝病毒ayw复制和表达的细胞培养模型HepG2 2.2.15细胞系中观察了RNA干扰对乙肝病毒复制的影响。本研究的目的是调查靶向乙肝病毒mRNA的短发夹RNA(shRNA)对HepG2 2.2.15细胞中病毒复制的影响。我们选择了具有不同假定二级结构的三个乙肝病毒mRNA靶区域,以测试RNA的二级结构是否可能影响对靶乙肝病毒RNA的抑制效果。设计了三种乙肝病毒特异性小干扰RNA(siRNA),分别靶向X(1689 - 1708)、核心(2229 - 2248)和S(765 - 784 nt)转录本。将分别靶向S、核心和X区域的表达shRNA的质粒P765、P2229和P1689或靶向lacZ基因的空质粒转染到HepG2 2.2.15细胞中。转染后六天内收集培养基并通过实时PCR进行分析。病毒DNA产生被抑制了7天。使用P765、P2229和P1689载体时,乙肝病毒DNA水平分别降低了73%、72%和79%。总之,针对X、核心和S区域设计的shRNA特异性且显著地抑制了乙肝病毒DNA。siRNA可能可用于治疗乙型肝炎。