检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:陈思穆[1] 韩剑锋[1] 曾琴[1] 万瑜[1] 孙逊[1]
机构地区:[1]四川大学华西药学院靶向药物与释药系统教育部重点实验室,四川成都610041
出 处:《华西药学杂志》2012年第6期662-665,共4页West China Journal of Pharmaceutical Sciences
摘 要:目的提高重组腺病毒在细胞中,特别是缺乏柯萨奇腺病毒受体的细胞中的转染效率。方法将阳离子材料聚乙烯亚胺PEI与重组腺病毒通过电荷作用形成复合物,用激光粒度仪及电位分析仪测定其粒径和电位;以表达β半乳糖苷酶的重组腺病毒作为模型病毒,研究其在富含(A549)或者缺乏(MDCK、LLC)柯萨奇腺病毒受体细胞中的转染效率和毒性,并用荧光标记复合物,观察其进入细胞的能力。结果与聚乙烯亚胺结合形成复合物可明显促进腺病毒进入细胞的能力,从而提高腺病毒在各种细胞中的转染效率,同时发现小分子的PEI-2 kD由于其较好的生物相容性,对腺病毒进入细胞后的传递影响较小,所以最终的基因传递效率要显著优于PEI-25 kD;PEI-2 kD在本复合物中表现出的细胞毒性要小于PEI-25 kD。结论PEI-2 kD可以用于病毒载体和非病毒载体结合的基因传递研究。OBJECTIVE To enhance the transduction efficiency of adenovirus on cells,especially on coxsackievirus and adenovirus receptor(CAR) deficient cells.METHODS Adenovirus was combined with cationic material,polyethylenimine(PEI) through charge interaction to form complexes as new gene vector.The particle size and Zeta potential of the complexes were measured by photon correlation spectroscopy.And the transduction efficiency and cytotoxicity were analyzed on CAR overexpressed(A549) or down-regulated(MDCK) cells by using recombinant adenovirus expressing β-galactosidase.The fluorescence labeled complexes were also tested for their cell enter ability.RESULTS Combination with PEI to form complexes could significantly enhance cell uptake of adenovirus,thus increased the gene transfer efficiency.Additionally,we found that PEI-2 kD as a low molecular PEI incorporated in Ad/PEI,had less cytotoxicity and higher biocompatibility,more importantly,less effect on the intracellular transfer of adenovirus,like endosome escape and nuclear localization,and subsequently higher gene transfer compared with PEI-25 kD.CONCLUSION PEI-2 kD is a useful material in the combination of viral and non-viral gene delivery strategy.
分 类 号:R915[医药卫生—微生物与生化药学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.117