Zeng Xian-Cheng, Zhang Tong, Huang De-Hao, Wang Guo-Ying, Chen Wei, Li Hua, Zhang Jian, Fang Tian-Ling, Zhang Qi, Chen Gui-Hua
Department of Hepatobiliary Surgery, Zengcheng People,s Hospital (BoJi-Affiliated Hospital, Sun Yat-Sen University), Guangzhou, China.
Ann Clin Lab Sci. 2013 Spring;43(2):135-44.
Up-regulation of Human Leukocyte Antigen-G (HLA-G) expression is thought to contribute to the escape in immune surveillance by suppressing natural killer (NK) cell function. However, little is known about the expression of HLA-G in hepatocellular carcinoma (HCC) and its relationship to NK cell-mediated cytotoxicity. In this study, we aimed to investigate the expression of HLA-G in human HCC cell lines and determine whether its expression was related to inhibition of NK cell cytolysis.
The levels of HLA-G gene expression in human HCC cell lines were assessed by indirect immunofluorescence analysis (IFA), Real time RT-PCR and Western Blot. Vectors containing small interfering RNA (siRNA) specifically targeting the HLA-G gene were constructed and applied to diminish HLA-G expression. The cells were examined by flow cytometry and fluorescent microscope 24 h after transfection as well as 2-3 weeks after G418 selection. The steady-state levels of HLA-G mRNA and protein were then checked by real time RT-PCR and Western Blot analysis, respectively. A nonradioactive cytotoxicity assay was used to evaluate the effect of HLA-G on NK-mediated cytotoxicity against the siRNA treated cells.
Both HLA-G mRNA and protein can be detected in human HCC cell lines. Levels of HLA-G mRNA and protein were diminished 88.73% and 75.91% respectively by targeting siRNA. In the stable HLA-G gene knock-down cell lines, a significant increase in NK cell-mediated lysis occurred.
Abnormal expression of HLA-G in HCC cell lines plays an important role in protecting against NK cell attack. The significant correlation between HLA-G expression and NK cell lysis implies that the abnormal expression of HLA-G might contribute to the mechanism of escape from host immune surveillance in HCC.
人类白细胞抗原G(HLA-G)表达上调被认为通过抑制自然杀伤(NK)细胞功能而有助于免疫逃逸。然而,关于HLA-G在肝细胞癌(HCC)中的表达及其与NK细胞介导的细胞毒性之间的关系知之甚少。在本研究中,我们旨在研究HLA-G在人肝癌细胞系中的表达,并确定其表达是否与NK细胞溶解抑制有关。
通过间接免疫荧光分析(IFA)、实时逆转录聚合酶链反应(Real time RT-PCR)和蛋白质免疫印迹法(Western Blot)评估人肝癌细胞系中HLA-G基因的表达水平。构建了特异性靶向HLA-G基因的小干扰RNA(siRNA)载体,并用于降低HLA-G的表达。转染后24小时以及G418处理2-3周后,通过流式细胞术和荧光显微镜检查细胞。然后分别通过实时逆转录聚合酶链反应和蛋白质免疫印迹分析检测HLA-G mRNA和蛋白质的稳态水平。采用非放射性细胞毒性试验评估HLA-G对NK介导的针对siRNA处理细胞的细胞毒性作用。
在人肝癌细胞系中均可检测到HLA-G mRNA和蛋白质。靶向siRNA后,HLA-G mRNA和蛋白质水平分别降低了88.73%和75.91%。在稳定的HLA-G基因敲低细胞系中,NK细胞介导的细胞溶解显著增加。
HLA-G在肝癌细胞系中的异常表达在抵抗NK细胞攻击中起重要作用。HLA-G表达与NK细胞溶解之间的显著相关性表明,HLA-G的异常表达可能有助于肝癌逃避宿主免疫监视的机制。