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作 者:石卓[1] 舒强[1] 赵正言[1] 陈智[2] 姚航平[2] 方向明[3]
机构地区:[1]浙江大学医学院附属儿童医院胸外科,浙江杭州310003 [2]浙江大学医学院附属第一医院传染病研究所,浙江杭州310003 [3]浙江大学医学院附属第一医院麻醉科,浙江杭州310003
出 处:《浙江大学学报(医学版)》2006年第6期590-595,共6页Journal of Zhejiang University(Medical Sciences)
基 金:国家自然科学基金(A30070854);浙江省科技厅基金项目(001103241)
摘 要:目的:探讨重组腺病毒载体在真核细胞中稳定表达阳离子抗菌肽——β-防御素2的可行性。方法:采用RT-PCR方法扩增得到大鼠β-防御素2(rBD 2)基因片段,定向插入到腺病毒穿梭质粒pShuttle-CMV中,重组质粒pShuttle-CMV-rBD 2转化E.coli B J5183-AD-1后,与腺病毒基因组质粒pA dE asy-1发生同源重组,重组质粒pA dE asy-rBD 2转染293细胞进行腺病毒表达载体的包装。将包装成功的腺病毒感染cos-7细胞,并建立SD大鼠腺病毒感染模型,进行β-防御素2多肽的体外和体内表达,采用W estern b lot与免疫组化方法检测其表达。结果:重组腺病毒表达载体构建成功,包含大鼠β-防御素2基因,滴度达到109PFU/m l,W estern b lot与免疫组化方法分别检测到β-防御素2在SD大鼠体外、体内的表达。结论:重组腺病毒载体能在真核细胞中稳定表达阳离子抗菌肽——β-防御素2。Objective: To explore the possibility of stable expression of cationic peptide β-defensin-2 in eukaryocytes with adenovirus vector. Methods: The rat β-defensin-2 (rBD2) gene was cloned at the downstream of CMV promoter of the adenoviral shuttle plasmid pShuttle-CMV. Then pShuttle-CMV-rBD2 was transformed into E.coli BJ5183-AD-1, in which recombination occurred between plasmids and pAdEasy-1 to construct pAdEasy-rBD2. After confirmation by endonuclease, linear pAdEasy-rBD2 was transformed into 292 cells to obtain packaged adenoviral expression vector, which was used to infect cos-7 cells and to establish respiratory adenovirus infection model of rat. The in vivo and in vitro expression activity of recombinant adenovirus was detected by Western blot and immunohistochemistry. Results: The inserted DNA of pShuttle-CMV-rBD2 consisted of rat β-defensin 2 gene. The pathological effect of infected cells, electronic microscopic observation and PCR showed that the recombinant adenovirus vector was constructed successfully. The concentration of the adenovirus was 10^9PFU/ml. The vector expressed rat β-defensin-2 efficiently in vivo and in vitro. Conclusion: The recombinant adenovirus vector can express cationic peptide β-defensin-2 in eukaryocytes.
关 键 词:防御素类/遗传学 腺病毒 人/遗传学 免疫组织化学 基因表达 Β-防御素 抗菌肽 腺病毒表达载体 基因重组 基因治疗
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