Wang Q, Jia X C, Finer M H
Cell Genesys Inc, Foster City, CA 94404, USA.
Gene Ther. 1995 Dec;2(10):775-83.
A cell line that provides the E1 as well as the E4 gene functions of human adenovirus 5 has been established by introduction of the full-length Ad5 E4 region into 293 cells. To avoid the E1A transactivation of the E4 gene expression, the E4 promoter was replaced by the mouse alpha inhibin promoter containing a cAMP response element. This cell line was used to generate E1/E4-deleted adenovirus vectors containing a lacZ gene in the E1 region under the control of mouse pgk promoter. The titer and the lacZ gene expression of E1/E4-deleted adenovirus vector were comparable to those of E1-deleted vectors. Evidence of cytopathic effect was absent following infection of nonpermissive cell lines with E1/E4-deleted adenovirus in vitro. Establishment of the 293-E4 cell line and the generation of E1/E4-deleted adenovirus vectors may prolong gene expression in vivo and significantly improve the safety of adenovirus vectors for human gene therapy.
通过将全长Ad5 E4区域导入293细胞,建立了一种提供人腺病毒5的E1以及E4基因功能的细胞系。为避免E1A对E4基因表达的反式激活作用,将E4启动子替换为含有cAMP反应元件的小鼠α抑制素启动子。该细胞系用于产生E1/E4缺失的腺病毒载体,其在E1区域含有一个受小鼠pgk启动子控制的lacZ基因。E1/E4缺失的腺病毒载体的滴度和lacZ基因表达与E1缺失的载体相当。在体外,用E1/E4缺失的腺病毒感染非允许细胞系后未出现细胞病变效应的证据。293-E4细胞系的建立和E1/E4缺失的腺病毒载体的产生可能会延长体内基因表达,并显著提高腺病毒载体用于人类基因治疗的安全性。