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Overexpression of Ad5 precursor terminal protein accelerates recombinant adenovirus packaging and amplification in HEK-293 packaging cells

机译:Ad5前体末端蛋白的过表达加速了HEK-293包装细胞中重组腺病毒的包装和扩增

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Recombinant adenoviruses are one of the most common vehicles for efficient in vitro and in vivo gene deliveries. Here, we investigate whether exogenous precursor terminal protein (pTP) expression in 293 cells improves the efficiency of adenovirus packaging and amplification. We used a piggyBac transposon-based vector and engineered a stable 293 line that expresses high level of Ad5 pTP, designated as 293pTP. Using the AdBMP6-GLuc that expresses green fluorescent protein (GFP), BMP6 and Gaussia luciferase, we found that the infectivity of AdBMP6-GLuc viral samples packaged in 293pTP cells was titrated up to 19.3 times higher than that packaged in parental 293 cells. AdBMP6-GLuc viral samples packaged in 293pTP cells exhibited significantly higher transduction efficiency in 143B and immortalized mouse embryonic fibroblast (iMEF) cells, as assessed by fluorescence-activated cell sorting analysis of GFP-positive cells, the luciferase activity assay and BMP6-induced osteogenic marker alkaline phosphatase activities in iMEFs. When adenovirus amplification efficiency was analyzed, we found that 293pTP cells infected with AdBMP6-GLuc yielded up to 12.6 times higher titer than that in parental 293 cells, especially at lower multiplicities of infection. These results strongly suggest that exogenous pTP expression may accelerate the packaging and amplification of recombinant adenoviruses. Thus, the engineered 293pTP cells should be a superior packaging line for efficient adenovirus production.
机译:重组腺病毒是有效进行体外和体内基因递送的最常见载体之一。在这里,我们调查293细胞中外源性前体末端蛋白(pTP)的表达是否提高了腺病毒包装和扩增的效率。我们使用了基于PigBac转座子的载体,并设计了稳定的293品系,该品系表达高水平的Ad5 pTP,称为293pTP。使用表达绿色荧光蛋白(GFP),BMP6和高斯荧光素酶的AdBMP6-GLuc,我们发现包装在293pTP细胞中的AdBMP6-GLuc病毒样品的感染力被滴定,最高比亲本293细胞包装的病毒高19.3倍。封装在293pTP细胞中的AdBMP6-GLuc病毒样品在143B和永生化的小鼠胚胎成纤维细胞(iMEF)细胞中表现出明显更高的转导效率,这是通过GFP阳性细胞的荧光激活细胞分选分析,萤光素酶活性测定和BMP6诱导的成骨作用来评估的iMEF中的标记碱性磷酸酶活性。当分析腺病毒的扩增效率时,我们发现感染AdBMP6-GLuc的293pTP细胞的滴度比亲代293细胞高出12.6倍,尤其是在较低的感染复数下。这些结果强烈暗示外源pTP表达可以加速重组腺病毒的包装和扩增。因此,工程化的293pTP细胞应该是高效生产腺病毒的优良包装生产线。

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