转染
小发夹RNA
细胞毒性
分子生物学
细胞培养
下调和上调
细胞
细胞毒性T细胞
化学
免疫系统
人类白细胞抗原
自然杀伤细胞
癌症研究
生物
免疫学
抗原
体外
基因
生物化学
基因敲除
遗传学
作者
Nazanin Nazari,Shirin Farjadian
出处
期刊:DOAJ: Directory of Open Access Journals - DOAJ
日期:2016-09-01
卷期号:13 (3): 178-85
被引量:8
摘要
HLA-G is a nonclassical HLA class I molecule which, when elevated in tumor cells, is one of the main factors involved in tumor evasion of immune responses including NK and T cells.To evaluate the effect of HLA-G downregulation on NK cell cytotoxicity in tumor cell lines.The expression level of HLA-G was measured by real-time PCR and flowcytometry after transfection of SKOV3 by shRNA.1, which targets specific sequences in exon 4, or shRNA.2, which targets both exons 4 and 6. NK-92MI cell cytotoxicity against transfected or untransfected target cell lines was measured with the lactate dehydrogenase (LDH) release assay. The Jeg-3 cell line was used as a positive control.Membrane-bound HLA-G expression levels decreased significantly in both cell lines after transfection with both shRNAs compared to their corresponding untransfected cells (p<0.05). Jeg-3 cells were better lysed than SKOV3 cells by NK cells during the first 48 h after transfection with both shRNAs. Compared to untransfected cells, shRNA.1-transfected SKOV3 cells were significantly more lysed by NK cells 24 h post-transfection (p=0.043).As a clinical approach, HLA-G downregulation with shRNA may be effective in cancer therapy by improving immune cell activation.
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