南方医科大学学报 ›› 2006, Vol. 26 ›› Issue (04): 398-401.

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小分子干扰RNA靶向抑制suvivin基因诱导U251细胞凋亡的实验研究

徐如祥; 涂艳阳; 姜晓丹; 封江南; 黄俊;   

  1. 南方医科大学珠江医院神经外科/广东省神经医学研究所; 武汉市晶赛生物工程技术有限公司; 武汉市晶赛生物工程技术有限公司 广东 广州 510282; 广东 广州 510282; 湖北 武汉 430074;
  • 出版日期:2006-04-20 发布日期:2006-04-20
  • 基金资助:
    国家自然科学基金(30170961)~~

Apoptosis of glioma cell line U251 induced by small interfering RNA targeting survivin

XU Ru-xiang, TU Yan-yang, JIANG Xiao-dan, FENG Jiang-nan, HUANG Jun Department of Neurosurgery and Institute of Neuroscience of Guangdong Province, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, China; Gensil Bio-technology Limited Company of Wuhan, Wuhan 430074, China   

  1. 南方医科大学珠江医院神经外科/广东省神经医学研究所; 武汉市晶赛生物工程技术有限公司; 武汉市晶赛生物工程技术有限公司 广东 广州 510282; 广东 广州 510282; 湖北 武汉 430074;
  • Online:2006-04-20 Published:2006-04-20

摘要: 目的构建靶向survivin基因的小分子干扰RNA(siRNA)表达载体,导入人胶质瘤细胞U251中,研究siRNA靶向抑制survivin基因对U251细胞的凋亡诱导作用。方法根据siRNA设计原则,在survivin全长序列中选取设计含19个核苷酸(19nt)靶序列两条反向重复序列,间以9个核苷酸的茎环序列,两端分别加上对应的酶切位点,形成siRNA的 DNA模板并克隆到siRNA表达载体pGenesil-1中,获得靶向抑制survivin基因的siRNA表达载体pGenesil-1/survivin; 采用Metafectene转染试剂将干扰质粒导入到胶质瘤细胞U251;分别采用实时荧光定量PCR以及Western bloting从 mRNA和蛋白水平检测干扰效果;采用Annexin-V/PI双色标记的流式细胞仪法检测siRNA诱导的细胞凋亡。结果实时荧光定量PCR以及Western blotting显示:survivin基因的mRNA转录水平以及蛋白水平的表达均得到显著抑制;流式细胞仪检测结果显示:survivin基因表达被抑制后,U251细胞凋亡率明显增高。结论靶向survivin基因的重组siRNA 干扰载体pGenesi-1/survivin介导的RNAi显著靶向抑制了survivin基因在人胶质瘤细胞U251中的表达,并明显诱导了U251细胞发生凋亡。

Abstract: Objective To construct recombinant expression vectors of small interfering RNA (siRNA) targeting survivin and investigate apoptosis of glioma cell line U251 mediated by the survivin-targeting siRNA. Methods According to the sequence of the coding region of survivin gene, two strings of 19 nucleotides of inverted sequence flanking the loop sequence of two complementary 9-base oligonucleotides were designed and synthesized to form hairpin construct as the DNA templates for the target siRNA. The siRNA templates were cloned into siRNA expression vector pGenesil-1, and the resulted vector pGenesil-1/survivin was transfected into U251 cells using Metafectene following the standard protocols. Real-time PCR and Western blotting were performed to evaluate survivin gene silencing induced by siRNA transfection at the RNA and protein levels, respectively. Flow cytometry analysis with Annexin-V/PI double staining was used to determine the cell apoptosis. Results Real-time RT-PCR and Western blotting revealed significantly lowered survivin expression at both RNA and protein levels in transfected U251 cells, which exhibited a significantly higher apoptosis rate after transfection as shown by flow cytometry analysis. Conclusion RNA interference mediated by the siRNA expression vector pGenesi-1/survivin can significantly reduce survivin expression and induce remarkable apoptosis in U251 cells. 

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