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作 者:张巨峰[1,2] 樊东升[3] 张超[1] 卢彦欣[1] 王俊伟[2] 牟艳芳[2] 陈艳娜[2] 万峻[1]
机构地区:[1]深圳北京大学香港科技大学医学中心生物医学研究所,广东深圳518036 [2]广东药学院生命科学与生物制药学院,广东广州510006 [3]内蒙古医学院附属第二医院骨科,内蒙古呼和浩特010050
出 处:《现代生物医学进展》2010年第2期205-207,共3页Progress in Modern Biomedicine
基 金:教育部中国博士后科学基金(20080440778);深港创新圈计划(08fz-11)
摘 要:目的:构建携带单纯疱疹病毒脱氧胸腺嘧啶激酶基因(herpes simplex virus thymidine kinase,HSV-TK)的逆转录病毒,用于宫颈癌的治疗研究。方法:用限制性内切酶从质粒pcDNA3.1/HA-myc-His(-)Z-TK切下HSV-1TK cDNA序列,亚克隆入逆转录病毒载体pLXSN得到重组质粒pLXSN-TK,鉴定正确的阳性重组质粒经PA317细胞包装,G418筛选,在NIH3T3细胞进行病毒滴度测定。然后用病毒感染人宫颈癌细胞HeLa。PCR、RT-PCR和Western blotting方法检测HSV-1TK基因在HeLa中的整合和表达情况。结果:重组质粒pLXSN-TK经PA317细胞包装后收获病毒上清,感染HeLa细胞,检测发现HSV-1TK基因整合到细胞基因组DNA中,并且能有效的转录和翻译。结论:成功构建了逆转录病毒pLXSN-TK,该病毒能有效感染HeLa细胞,并使携带的治疗基因HSV-1TK在细胞中表达,为今后HSV-1TK基因治疗宫颈癌的研究奠定基础。Objective:To construct the recombinant retrovirus carrying herpes simplex virus thymidine kinase-1(HSV-1TK) gene and to observe the expression of HSV-1TK in cervical carcinoma cell line HeLa. Methods:The HSV-1TK cDNA was digested by restriction endonuclease from plasmid pcDNA3.1/HA-myc-His(-) Z-TK and then directionally inserted into retroviral vector pLXSN to construct recombinant plasmid pLXSN-TK. The pLXSN-TK was transferred into retroviral producer cell line PA317 for packaging retrovirus and then the resultant retrovirus was applied to infected the HeLa cells. The integration of HSV-1TK gene into the HeLa cells genome was assayed by PCR. The expression of HSV-1TK gene was detected by RT-PCR and Western blot. Results:The HSV-1TK gene was integrated into the genome of HeLa cells shown by results of PCR after retroviral infection. The expression of HSV-1TK gene was confirmed by RT-PCR and Western blotting. Conclusion:The recombinant retrovirus carrying HSV-1TK gene was constructed successfully and may be a potentially effective strategy for the treatment of cervical cancer.
关 键 词:单纯疱疹病毒脱氧胸腺嘧啶激酶基因 逆转录病毒 宫颈癌
分 类 号:R332[医药卫生—人体生理学] R322.61[医药卫生—基础医学]
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