首页> 美国卫生研究院文献>World Journal of Gastroenterology >Lethiferous effects of a recombinant vector carrying thymidine kinase suicide gene on 2.2.15 cells via a self-modulating mechanism
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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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摘要

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 pcDNA3-SCITK or vector pcDNA3-SCI which was used as the mock plasmid. The HepG2 cells transfected with pcDNA3-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 pcDNA3-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 pcDNA3-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 pcDNA3-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细胞的致死作用及可能的自调控机制。方法:通过插入携带有胸腺嘧啶激酶(TK)自杀基因的片段构建自调控表达质粒pcDNA3-SCITK。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,HCV的内部核糖体进入位点(IRES)元件和TK基因进入真核载体pcDNA3,在其中表达TK自杀基因受HBV S基因转录控制。 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pcDNA3-SCITK或用作模拟质粒的载体pcDNA3-SCI转染。用pcDNA3-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)。转染后第1天,第3天和第6天通过ELISA检测细胞培养上清液中的HBsAg水平。同时,在转染后第6天,通过照片记录转染细胞的形态,并通过锥虫蓝排斥试验评估存活细胞的比例。结果:pcDNA3-SCITK的结构准确性通过限制性内切酶消化,特异性引物PCR和DNA测序证实。转染后第6天,转染2.2.15细胞培养上清液中的HBsAg水平较对照组明显降低(P <0.05)。 pcDNA3-SCITK表达对2.2.15细胞的致死作用最初在转染后的第3天被发现,并在转染后的第6天加剧。观察到大多数转染的2.2.15细胞萎缩,圆形,甚至死亡。通过锥虫蓝排斥试验评估,转染后第6天存活细胞比例在阴性对照组中为95%,在实验组中仅为11%。结论:结果表明自杀pcDNA3-SCITK的基因表达只能响应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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