壳寡糖纳米载体细胞内递送EGFR脱氧核酶的研究  

Experimental Study of the Oligochitosan Nanoparticles of Intracellular EGFR DNAzyme Delivery

作　　者：李丹[1] 王贝[1] 林奕婷[1] 靳冉[1] 刘志文[1] 刘选明[1] 

机构地区：[1]湖南大学生物学院,生物能源与材料研究中心,湖南长沙410082

出　　处：《湖南大学学报（自然科学版）》2010年第11期51-54,共4页Journal of Hunan University:Natural Sciences

基　　金：湖南省普通高校青年骨干教师培养对象资助项目(521298462)

摘　　要：设计靶向EGFR mRNA的脱氧核酶(EGFR DRz),以壳寡糖(COS)为材料,建立了一种有效的纳米基因细胞内传递体系,并研究其介导的靶向EGFR的脱氧核酶在Hela细胞内的生物学效应.流式结果表明COS-EGFR DRz复合体转染效率为88.7%,与脂质体转染试剂的89.7%相比无显著差异.半定量RT-PCR结果显示,经壳寡糖纳米载体递送的EGFR DRz能有效地靶向切割Hela细胞内的EGFR mRNA,使其表达下降.进一步的流式分析显示细胞被阻滞在G0～G1期,并且出现凋亡现象,其中COS组的凋亡率为19.3%,大于对照组脂质体的凋亡率13.0%.研究表明,COS较脂质体有相似的转染效率和更低的毒性,是一种潜在的、有效的脱氧核酶递送载体.A new intracellular gene delivery system based on oligochitosan（COS）was prepared and proven to be effective.First of all,The DNAzyme targeting EGFR（EGFR DRz）was designed and synthesized.Then,the biological effect of the EGFR DRz delivery system based on COS was studied in Hela cell with Flow Cytometry.It was shown that there was no statistically significant difference in transfection efficiency between liposome transfection reagent（89.7%）and COS-EGFR DRz（88.7%）.The results of semiquantitative RT-PCR confirmed that the EGFR mRNA in Hela cell could be cleaved by targeting COS-EGFR DRz.The cell cycle analysis in Hela cells transfected with COS-EGFR DRz revealed an arrestment in the G0/G1phase.And the cell apoptosis rate induced by COS-EGFR DRz was 19.3%,which was higher than the rate induced by liposome-EGFR DRz（13.0%）.These results have demonstrated that COS possesses higher transfection efficiency and lower cytotoxicity.It will be a potential DNAzyme delivery system.

关 键 词：壳寡糖 脱氧核酶 EGFR 基因递送 

分 类 号：Q74[生物学—分子生物学]