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Lethiferous effects of a recombinant vector carrying thymidine kinase suicide gene on 2.2.15 cells via a self-modulating mechanism

机译:带有胸苷激酶自杀基因的重组载体通过自调节机制对2.2.15细胞的杀虫作用

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AIM: To determine the lethiferous effects of a recombinant vector carrying thymidine kinase (TK) suicide gene on 2.2.15 cells and the possible self-modulating mechanism. METHODS: A self-modulated expressive plasmid pcDNA3-SCITK was constructed by inserting the fragments carrying hepatitis B virus antisense-S (HBV-anti-S) gene, hepatitis C virus core (HCV-C) gene, internal ribosome entry site (IRES) element of HCV and TK gene into the eukaryotic vector pcDNA3, in which the expression of TK suicide gene was controlled by the HBV S gene transcription. 2.2.15 cells that carry the full HBV genome and stably express series of HBV antigen were transfected with pcDNA_3-SCITK or vector pcDNA_3-SCI which was used as the mock plasmid. The HepG2 cells transfected with pcDNA_3-SCITK were functioned as the negative control. All the transfected cells were incubated in DMEM medium supplemented with 10 μg/ml. of ganciclovir (GCV). The HBsAg levels in the supernatant of cell culture were detected by ELISA on the 1st, 3rd and 6th day post-transfection. Meanwhile, the morphology of tranfected cells was recorded by the photograph and the survival cell ratio was assessed by the trypan blue exclusion test on the 6th day post-transfection. RESULTS: The structural accuracy of pcDNA_3-SCITK was confirmed by restriction endonuclease digestion, PCR with specific primers and DNA sequencing. The HBsAg levels in the supernatant of transfected 2.2.15 cell culture were significantly decreased on the 6th day post-transfection as compared with that of the mock control (P<0.05). The lethiferous effect of pcDNA_3-SCITK expression on 2.2.15 cells was initially noted on the 3rd day after transfection and aggravated on the 6th day post transfection, in which the majority of transfected 2.2.15 cells were observed shrunken, round in shape and even dead. With assessment by the trypan blue exclusion test, the survival cell ratio on the 6th day post transfection was 95 % in the negative control and only 11 % in the experimental group. CONCLUSION: The results indicate that suicide gene expression of pcDNA_3-SCITK can only respond to HBV-S gene transcription, which may be potentially useful in the treatment of HBV infection and its related liver malignancies.
机译:目的:确定带有胸苷激酶(TK)自杀基因的重组载体对2.2.15细胞的致死作用及其可能的自我调节机制。方法:通过插入携带乙型肝炎病毒反义-S(HBV-anti-S)基因,丙型肝炎病毒核心(HCV-C)基因,内部核糖体进入位点(IRES)的片段,构建自调控表达质粒pcDNA3-SCITK )将HCV和TK基因插入真核载体pcDNA3中,其中TK自杀基因的表达受HBV S基因转录的控制。 2.2.15携带完整HBV基因组并稳定表达一系列HBV抗原的细胞用pcDNA_3-SCITK或用作模拟质粒的载体pcDNA_3-SCI转染。用pcDNA_3-SCITK转染的HepG2细胞用作阴性对照。将所有转染的细胞在补充有10μg/ ml的DMEM培养基中孵育。更昔洛韦(GCV)。在转染后第1、3和6天通过ELISA检测细胞培养上清液中的HBsAg水平。同时,在照片上记录转染细胞的形态,并在转染后第6天通过台盼蓝排除试验评估存活细胞比率。结果:通过限制性内切酶消化,特异引物PCR和DNA测序证实了pcDNA_3-SCITK的结构准确性。转染后第6天,转染2.2.15细胞培养物上清液中的HBsAg水平较空白对照组明显降低(P <0.05)。转染后第3天最初注意到pcDNA_3-SCITK表达对2.2.15细胞的致死作用,转染后第6天加剧了pcDNA_3-SCITK表达的致死作用,其中观察到大部分转染的2.2.15细胞萎缩,圆形甚至均匀。死。通过锥虫蓝排除试验评估,转染后第6天的存活细胞比率在阴性对照组中为95%,在实验组中仅为11%。结论:pcDNA_3-SCITK自杀基因的表达仅能响应HBV-S基因的转录,这可能在治疗HBV感染及其相关的肝恶性肿瘤中可能有用。

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