华西口腔医学杂志

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表达人CD40配体的重组腺病毒载体的构建

吴红兵1,田 聆2,文艳君2,刘玉梅3,阚 兵2,杜小波2,徐健蓉2,魏于全2   

  1. 1.四川大学华西口腔医院 放射科;2.四川大学华西医院 生物治疗国家重点实验室与肿瘤中心; 3.四川大学华西附二院 产科,四川 成都610041
  • 收稿日期:2005-12-25 修回日期:2005-12-25 出版日期:2005-12-20 发布日期:2005-12-20
  • 通讯作者: 魏于全,Tel:028-85422564
  • 作者简介:吴红兵(1966-),男,四川人,讲师,现为四川大学华西临床医学院肿瘤专业博士研究生
  • 基金资助:
    国家自然科学基金资助项目(3013026)

Construction of the Recombinant Adenovirus Vector Expressing Human CD40 Ligand Gene

WU Hong-bing1,TIAN Ling2,WEN Yan-jun2,LIU Yu-mei3,KAN Bing2,DUXiao-bo2,XUJian-rong2,WEI Yu-quan2   

  1. 1.Dept.ofRadiology,West China College ofStomatology,Sichuan University,Chengdu610041,China;2.State Key.Laboratory of Biotherapy and Cancer Center,West China Hospital,Sichuan University,Chengdu610041,China;3.Dept.of Obstetrics and Gynecology,West China SecondHospital,Sichuan University,Chengdu610041,China
  • Received:2005-12-25 Revised:2005-12-25 Online:2005-12-20 Published:2005-12-20

摘要:

目的 构建含有hCD40L基因的重组腺病毒载体,为其在动物模型体内表达和肿瘤基因治疗提供基础。方法 用XhoⅠ、SwaⅠ双酶切质粒pORF-hCD40L,回收1 900 bp基因片段并定向克隆插入穿梭质粒pShuttle中 XhoⅠ、EcoRⅤ双酶切位点,得到重组质粒pShuttle-hCD40L。经PmeI酶切与腺病毒骨架质粒pAdEasy-1共转化 BJ5183细菌,同源重组后用选择培养基筛选阳性克隆,提取质粒PacI酶切线性化后用脂质体介导转染293细胞。酶切分析和PCR鉴定重组的腺病毒。结果 酶切分析、PCR验证表明,hCD40L基因成功克隆到腺病毒pAdEasy-1 载体中。结论 成功构建表达hCD40L基因的重组腺病毒载体,为进一步研究其在哺乳动物内表达及基因治疗提供了基础。

关键词: hCD40L基因, 腺病毒载体, DNA同源重组, 基因治疗

Abstract: Objective To construct a recombinant adenovirus vector expressing hCD40Lgene and explore it in the use of anti- tumor gene therapy.Methods 1 900 bp gene fragmentwas obtained form plasmid pORF-hCD40L byXhoⅠ/SwaⅠcutting and then cloned directionally into the pShuttle plasmid, finally, the resultant plasmid was digested by restriction endonnucleasePmeI and subsequently cotransformtion into BJ5183 cells with the adenoviral backbone pAdEasy-1 to obtain the homologous recombinant and then the recombinant was packaged in the 293 cells. Some methods such as PCR and endonulease digestionwere employed to identify the recombinant adenovirus.Results The evidences of endonulease digestion and PCR analysis confirmed that recombi- nant hCD40L gene was correctly inserted into adenovirus vector.Conclusion The adenoviral vector which expressed hCD40L gene was constructed. It provides an experimental basis for studies on it expression in the mammalian cells and in tumorgene ther- apy.

Key words: hCD40L gene, adenovirus vector, DNA homologous recombination, gene therapy