中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 36 Issue 1
Jan.  2020
Turn off MathJax
Article Contents

Effect of interferon-α and thymopentin on the mRNA expression of APOBEC3A and APOBEC3B in HepG2.2.15 cells

DOI: 10.3969/j.issn.1001-5256.2020.01.017
Research funding:

 

  • Received Date: 2019-08-13
  • Published Date: 2020-01-20
  • Objective To investigate the effect of synergistic intervention of interferonα(IFNα) and thymopentin(TP5) on the mRNA expression of apolipoprotein B mRNA editing enzyme,catalytic polypeptide-like 3 A(APOBEC3 A) and apolipoprotein B mRNA editing enzyme,catalytic polypeptide-like 3 B(APOBEC3 B) in HepG2. 2. 15 cells. Methods HepG2. 2. 15 cells were divided into blank control group,IFNα treatment group,TP5 treatment group,and IFNα + TP5 treatment group,and at 12,24,48,and 72 hours of treatment,quantitative real-time PCR was used to measure the mRNA expression of APOBEC3 A and APOBEC3 B in HepG2. 2. 15 cells. An analysis of variance was used for comparison of continuous data between multiple groups,and the least significant difference t-test was used for further comparison between two groups. Results Compared with the blank control group,the IFNα treatment group and the IFNα + TP5 treatment group had a significant increase in the mRNA expression of APOBEC3 A at 12,24,48,and 72 hours of treatment(all P < 0. 001). Compared with the IFNα treatment group,the IFNα + TP5 treatment group had a significant increase in the mRNA expression of APOBEC3 A at these four time points(all P < 0. 001). TP5 treatment had no significant influence on the mRNA expression of APOBEC3 A at each time point(all P > 0. 05). There was no significant difference in the mRNA expression of APOBEC3 B between the blank control group and the treatment groups(all P > 0. 05). Conclusion IFNα combined with TP5 can significantly upregulate the mRNA expression of APOBEC3 A in HepG2. 2. 15 cells.

     

  • loading
  • [1] NASSAL M. HBV cccDNA:Viral persistence reservoir and key obstacle for a cure of chronic hepatitis B[J]. J Clin Hepatol Gut,2015,64(12):1972-1984.
    [2] MA Y,BAO X,XIONG F,et al. The effect of thymopentin add-on in hepatitis B e antigen positive chronic hepatitis B after virus suppression by peginterferon plus entecavir therapy[J].Cell Mol Biol(Noisy-le-grand),2019,65(2):75-81.
    [3] SILVAS TV,SCHIFFER CA. APOBEC3s:DNA-editing human cytidine deaminases[J]. Protein Sci,2019,28(9):1552-1566.
    [4] LUCIFORA J,XIA Y,REISINGER F,et al. Specific and nonhepatotoxic degradation of nuclear hepatitis B virus cccDNA[J]. Science,2014,343(6176):1221-1228.
    [5] XIA Y,STADLER D,LUCIFORA J,et al. Interferon-gamma and tumor necrosis factor-alpha produced by T cells reduce the HBV persistence form,cccDNA,without cytolysis[J].Gastroenterology,2016,150(1):194-205.
    [6] LI Y,XIA Y,HAN M,et al. IFN-alpha-mediated base excision repair pathway correlates with antiviral response against hepatitis B virus infection[J]. Sci Rep,2017,7(1):12715.
    [7] HE X,LI J,WU J,et al. Associations between activation-induced cytidine deaminase/apolipoprotein B mRNA editing enzyme,catalytic polypeptide-like cytidine deaminase expression,hepatitis B virus(HBV)replication and HBV-associated liver disease(Review)[J]. Mol Med Rep,2015,12(5):6405-6414.
    [8] DING S,ROBEK MD. Cytidine deamination and cccDNA degradation:A new approach for curing HBV?[J]. Hepatology,2014,60:2118-2121.
    [9] LI Y,TIAN Y,YANG XM,et al. Effect of thymosinα1 on the function of CD4+CD25+CD127dim/-regulatory T cells in chronic hepatitis B patients[J]. J Clin Hepatol,2018,34(5):1011-1014.(in Chinese)李彧,田颖,杨晓梅,等.胸腺肽α1对慢性乙型肝炎CD4+CD25+CD127dim/-调节性T淋巴细胞功能的影响[J].临床肝胆病杂志,2018,34(5):1011-1014.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (1030) PDF downloads(235) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return