Teramoto S, Matsuse T, Ohga E, Nagase T, Fukuchi Y, Ouchi Y
Department of Geriatrics, Tokyo University Hospital, Japan.
Life Sci. 1997;61(9):891-7. doi: 10.1016/s0024-3205(97)00591-2.
Many features of Ad-mediated gene transfer to human lung fibroblasts are not well understood. We tested kinetics of transduction efficiency of LacZ gene to human lung fibroblasts by E1-deleted adenovriuses containing two different promoters, i.e. CMV and RSV LTR. A dose-dependent relationship between the vector multiplicity of infection (moi) and the efficiency of LacZ gene transfer to fibroblasts was observed with each vector, and higher moi of vectors achieved 100% of transduction efficiency. Further, Ad-mediated gene transfer was enhanced by a long period of vector exposure to fibroblasts up to 6 hours. There were no differences in transduction efficiency between the two Ad vectors. LacZ gene expression by Ad vectors consistently decreased one day after infection. These results indicate that both Ad vectors are equally effective for gene transfer to human lung fibroblasts, and higher moi of vectors and/or a longer period exposure of fibroblasts to vectors can facilitate more efficient transduction of LacZ reporter gene into human lung fibroblasts.
腺病毒介导的基因转移至人肺成纤维细胞的许多特性尚未得到充分了解。我们通过含有两种不同启动子(即巨细胞病毒(CMV)和劳斯肉瘤病毒长末端重复序列(RSV LTR))的E1缺失腺病毒,测试了LacZ基因导入人肺成纤维细胞的转导效率动力学。每种载体均观察到感染复数(moi)与LacZ基因向成纤维细胞的转移效率之间存在剂量依赖性关系,且载体的较高moi可实现100%的转导效率。此外,长达6小时的载体与成纤维细胞长时间接触可增强腺病毒介导的基因转移。两种腺病毒载体的转导效率没有差异。感染后一天,腺病毒载体介导的LacZ基因表达持续下降。这些结果表明,两种腺病毒载体在将基因转移至人肺成纤维细胞方面同样有效,且载体的较高moi和/或成纤维细胞与载体的较长接触时间可促进LacZ报告基因更有效地导入人肺成纤维细胞。