Wengenmayer Tobias, Poehlmann Tobias G, Markert Udo R
Placenta Laboratory, Department of Obstetrics, Friedrich-Schiller University, Jena, Germany.
Am J Reprod Immunol. 2004 Mar;51(3):189-91. doi: 10.1111/j.1600-0897.2004.00150.x.
Human leukocyte antigen-G (HLA-G) plays a major role in escape of trophoblast cells from maternal cytotoxicity. Unless its malignant transformation, Jeg-3 choriocarcinoma cell line maintained the capacity of HLA-G production. For the analysis of function and mechanisms of HLA-G-induced immune regulation, a human cellular model with suppressed HLA-G would be very helpful. RNA interference (RNAi) is a very elegant method for this approach, but the design of appropriate oligonucleotide sequences may provide difficulties. We designed oligonucleotides to interfere exclusively with HLA-G mRNA, which were applied at different concentrations to 50% confluent Jeg-3 cells. After 36 hr, the HLA-G content in Jeg-3 cells was analyzed by Western blots. Applying the described RNAi method and oligonucleotides the cellular content of HLA-G was dose-dependently reduced as assessed in several independent Western blots. This method provides a tool for extensive investigation of HLA-G functions in vitro and if vivo.
人类白细胞抗原G(HLA-G)在滋养层细胞逃避母体细胞毒性的过程中起主要作用。除非发生恶性转化,JEG-3绒毛膜癌细胞系保持HLA-G产生的能力。为了分析HLA-G诱导的免疫调节的功能和机制,一个HLA-G表达受抑制的人类细胞模型将非常有帮助。RNA干扰(RNAi)是实现这一方法的一种非常巧妙的手段,但设计合适的寡核苷酸序列可能存在困难。我们设计了专门干扰HLA-G mRNA的寡核苷酸,并将其以不同浓度应用于50%汇合的JEG-3细胞。36小时后,通过蛋白质印迹法分析JEG-3细胞中的HLA-G含量。应用所述的RNAi方法和寡核苷酸,通过多次独立的蛋白质印迹法评估,HLA-G的细胞含量呈剂量依赖性降低。该方法为体外及体内广泛研究HLA-G的功能提供了一种工具。