Liu Fang, He Cheng-Wei, Zhang Yue-Fei, Zhou Ke-Yuan
Institute of Biochemistry and Molecular Biology, The First Affiliated Hospital, Guangdong Medical College, Zhanjiang 524023, China.
Acta Pharmacol Sin. 2005 Feb;26(2):228-34. doi: 10.1111/j.1745-7254.2005.00529.x.
To evaluate a new plasmid mediated RNA interference (RNAi) system and investigate whether knock-down of bcl-xL by short hairpin RNA (shRNA) can induce apoptosis of human nasopharyngeal carcinoma (NPC) cell line CNE-2Z in vitro.
The plasmid containing mU6 promoter was subcloned to yield the pmU6 plasmid, recombinant plasmid expressing shRNA targeting bcl-xL gene was designed and constructed, and were co-transfected cells with green fluorescence protein expressing plasmid. Flow cytometry was used to evaluate transfection efficiency, and RT-PCR and Western blot were applied to analyze bcl-xL mRNA and protein levels, respectively.
The shRNA expressed by the recombinant plasmid efficiently suppressed bcl-xL gene expression and induced apoptosis of NPC cells in vitro.
The recombinant plasmid can sufficiently mediate RNAi in CNE-2Z cells, and knock-down of the bcl-xL expression by shRNA significantly induced apoptosis in CNE-2Z cells. The results suggest this new system, mediated RNAi can be used as a tool for the study of gene function and gene therapy.
评估一种新的质粒介导的RNA干扰(RNAi)系统,并研究短发夹RNA(shRNA)敲低bcl-xL是否能在体外诱导人鼻咽癌(NPC)细胞系CNE-2Z凋亡。
将含有mU6启动子的质粒亚克隆以产生pmU6质粒,设计并构建表达靶向bcl-xL基因的shRNA的重组质粒,并与表达绿色荧光蛋白的质粒共转染细胞。采用流式细胞术评估转染效率,分别应用RT-PCR和Western blot分析bcl-xL mRNA和蛋白水平。
重组质粒表达的shRNA有效抑制了bcl-xL基因表达,并在体外诱导了NPC细胞凋亡。
重组质粒能在CNE-2Z细胞中充分介导RNAi,shRNA敲低bcl-xL表达显著诱导CNE-2Z细胞凋亡。结果表明,这种新的介导RNAi的系统可作为研究基因功能和基因治疗的工具。