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Construction and identification of Fas-targeting siRNA-expressing plasmid

机译:Fas靶向siRNA表达质粒的构建与鉴定

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摘要

Objective: To study the therapeutic potential of Fas inhibition in different diseases, a Fas-targeting siRNA (small interfering)-expressing plasmid was constructed. Methods: The U6 promoter cassette and siFas (small interfering RNA that inhibit Fas expression) template sequence were obtained by PCR method. They were cloned into modified pcDNA3.1. The resultant plasmid pU6-siFas was transfected into P815 cells with lipofectin2000 and selected under G-418-containing culture medium. Fas inhibition in stably transfected cells was detected by immunocytochemistry. Results: The plasmid pU6-siFas efficiently reduced the expression of Fas and conferred G-418 resistance in P815 cells. Conclusion: The successful construction of the siRNA expressing plasmid will facilitate the application of RNA interference technique and lay the foundation for further study of Fas inhibition in the treatment of different diseases such as aplastic anemia and acute liver failure.
机译:目的:研究Fas抑制在不同疾病中的治疗潜力,构建了一种靶向Fas的siRNA(小干扰)表达质粒。方法:通过PCR方法获得U6启动子盒和siFas(抑制Fas表达的小干扰RNA)模板序列。将它们克隆到修饰的pcDNA3.1中。用lipofectin2000将所得质粒pU6-siFas转染到P815细胞中,并在含G-418的培养基中选择。通过免疫细胞化学检测稳定转染的细胞中的Fas抑制。结果:质粒pU6-siFas有效降低了P815细胞中Fas的表达并赋予了G-418抗性。结论:siRNA表达质粒的成功构建将促进RNA干扰技术的应用,为进一步研究Fas抑制在治疗再生障碍性贫血和急性肝衰竭等疾病中的应用奠定基础。

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