人miR-146b慢病毒载体构建及人脂肪细胞中表达验证  

Construction of a recombinant lentiviral vector carrying miR-146b and validation of its transduction efficiency in human pre-adipocytes

作　　者：陈玲[1,2] 史春梅[1,2] 杨蕾[1,2] 朱璐[1] 徐广峰[1] 季晨博[2] 郭锡熔[1,2] 张春梅[2] 

机构地区：[1]南京医科大学儿科研究所,江苏南京210029 [2]南京医科大学附属南京妇幼保健院,江苏南京210004

出　　处：《中国儿童保健杂志》2013年第11期1155-1157,1160,共4页Chinese Journal of Child Health Care

基　　金：国家自然科学基金(81100619);江苏省医学创新团队项目(LJ201108);南京市科技发展计划(201104013)

摘　　要：目的构建人miR-146b慢病毒表达载体,包被病毒并检测其在人脂肪细胞中过表达效果。方法以人基因组DNA为模板,PCR高保真扩增包含miR-146b区域上下游各100bp左右的基因组DNA,亚克隆入慢病毒表达载体,与包装质粒共转染HEK-293T细胞,包装病毒,收取病毒上清,纯化后感染人脂肪前体细胞,36h开始观察荧光标记,72h收取细胞,抽提RNA,Realtime PCR检测慢病毒感染下miR-146b的相应表达量。结果成功构建人miR-146b慢病毒表达载体,包装获得的病毒感染人脂肪细胞的效率可达到85%以上,miR-146b过表达水平可接近4倍。结论本研究成功构建了人miR-146b慢病毒表达载体,包被的慢病毒可以在人脂肪细胞中实现过表达效果,为后续功能研究奠定了基础。Objective To construct a recombinant lentiviral vector carrying miR-146b and validate its infection efficien- cy in human pre-adipocytes. Methods The minigene fragment of miR-146b was amplified from human genomic DNA by PCR,then cloned into a lentivirus expression vector. After sequencing validated exactly, the expression plasmid and packaging plasmids Pcgvp,Rev,Vsvg were co-transfected into HEK-293T cells to produce lentivirus; the supernatant containing lentiviral particles was used to infect human preadipocytes, and its infection efficiency and miR-146b overexpression level were respectively tested by fluorescent observation and real-tirae quantitative PCR. Results MiR-46b lentiviral vector was constructed successfully,and infection efficiency in human pre-adipocytes reached over 85 %, the expression level increased nearly four folds. Conclusion We have successfully constructed the lentiviral vector containing miR-146b with high overexpression in infected human pre-adipocytes,which will be useful to the future studying the function of miR-146b in human pre-adipocytes.

关 键 词：miR-146b 慢病毒 人脂肪前体细胞 

分 类 号：R394[医药卫生—医学遗传学]