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机构地区:[1]西安交通大学医学院第二附属医院心胸外科,陕西西安710004
出 处:《西安交通大学学报(医学版)》2009年第6期766-768,共3页Journal of Xi’an Jiaotong University(Medical Sciences)
基 金:国家自然科学基金资助项目(No.30470456)~~
摘 要:目的构建假型逆转录病毒载体MuLV/VSV-G,并用于转染兔平滑肌细胞,为兔平滑肌细胞基因转染寻找一种高效的载体。方法构建含有报道基因lacZ的假型逆转录病毒载体MuLV/VSV—G,测定滴度,并转染兔平滑肌细胞,观察其转导效率。并与MuLV的转导效率进行比较。结果构建的MuLV/VSV-G载体,病毒滴度为6~7.8×10^6CFU,转染兔平滑肌细胞的效率是(92±12)%。而MuLV的转导效率为(24土5)%。结论成功构建了假型逆转录病毒载体MuLV/VSV-G载体,该载体作为一种高效的载体可用于兔平滑肌细胞基因转染。Objective To construct pseudotyped retroviral vector MuLV/VSV-G and transfer it into rabbit smooth muscle cells (SMC) in order to provide a high-efficiency vector for SMC gene transfer. Methods We constructed pseudotyped retroviral vector MuLV/VSV-G containing the previously reported gene lacZ, determined the titer, and determined the efficiency of gene transfer into SMC mediated by pseudotyped retroviral vector MuLV/VSV-G. Finally the transfer efficiency was compared with that by MuLV. Results MuLV/VSV-G vector was constructed. The titer of the vector was 6- 7.8 ×10^6CFU, the transfer efficiency was (92 ±12)% by using MuLV/VSV-G vector and (24±5)% by MuLV vector. Conclusion Pseudotyped retroviral vector MuLV/VSV-G which was constructed successfully is a kind of high-efficiency gene transfer vector in smooth muscle cells.
分 类 号:R373[医药卫生—病原生物学]
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