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包载TIMP-1重组腺病毒微球的制备及其对肝癌细胞增殖的抑制 被引量:6

Preparation of microsphere encapsulating recombinant TIMP-1 adenovirus and its inhibitory effects against hepatocellular carcinoma cells
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摘要 目的:制备携带人基质金属蛋白酶组织抑制因子-1(tissue inhibitors of metalloproteinase-1,TIMP-1)的重组腺病毒乳酸聚乙烯醇(poly-DL-lactide-poly,PELA)微球,探讨其对HepG2肝癌细胞增殖的影响。方法:采用溶剂挥发法双乳液体系,以可降解的生物材料PELA包被携带TIMP-1基因的重组腺病毒制成微球,测定其粒径、载病毒量、包封率及释放规律。重组腺病毒微球感染HepG2细胞,荧光显微镜观测感染效率,透射电镜观测超微结构,半定量RT-PCR检测TIMP-1mRNA表达;MTT法检测HepG2细胞增殖。结果:成功构建包载TIMP-1重组腺病毒的PELA微球,直径约1.965μm,包封率为60%,载病毒率为10.5×108efu/mg,在120h内释放病毒量接近60%,总的释放时间长于240h。空白微球无毒性PELA病毒微球感染HepG2细胞后,细胞稳定表达TIMP-1mRNA;对HepG2细胞的增殖有明显抑制作用,抑制率表达47%。结论:包载TIMP-1重组腺病毒的PELA微球可抑制肝癌HepG2细胞的增殖,为化学高分子载体运载基因治疗肝癌提供了实验依据。 Objective:To prepare poly-DL-lactide-poly (PELA) microspheres encapsulating recombinant tissue inhibitors of metalloproteinase-1 (TIMP-1) adenovirus,and to investigate their effects on the proliferation of hepatocellular carcinoma HepG2 cells.Methods:The microsphere was constructed by encapsulating recombinant adenovirus containing TIMP-1 in biodegradable PELA.The diameter of the microsphere,quantity of virus encapsulated,loading rate,and releasing kinetics were measured.HepG2 cells were infected with the microspheres;the infection efficiency was examined by fluorescent microscope;and the ultrastructure was observed by TEM.The expression of TIMP-1 mRNA in HepG2 cells was examined by semi-quantitative RT-PCR,and the proliferation of HepG2 cells was detected by MTT assay.Results:The microsphere encapsulating recombinant TIMP-1 adenovirus was successfully constructed,with its diameter,entrapment efficiency,and virus loading rate being 1.965,60.0%,and 10.5×108/mg,respectively.About 60% of the viruses were released within 120 h,and the total releasing time was longer than 240 h.Infection with rAdTIMP-1 PELA microsphere efficiently induced TIMP-1 expression in HepG2 cells,and significantly inhibited the proliferation of HepG2 cells,with the inhibitory rate being 47%.Conclusion:PELA microsphere encapsulating recombinant TIMP-1 adenovirus can markedly inhibit the proliferation of HepG2 cells,which provides an experimental basis for the combining macromolecular chemistry and gene therapy for treatment of hepatocellular carcinoma.
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 北大核心 2010年第1期57-61,共5页 Chinese Journal of Cancer Biotherapy
基金 四川省教育厅课题资助(No.2006B108) 四川省卫生厅课题资助(No.090210)~~
关键词 肝肿瘤 基质金属蛋白酶组织抑制因子 腺病毒 微球 基因治疗 hepatocellular carcinoma tissue inhibitors of metalloproteinase adenovirus microsphere gene therapy
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