Betts Zeynep, Dickson Alan J
The University of Manchester, Faculty of Life Sciences, Michael Smith Building, Manchester, United Kingdom.
Biotechnol J. 2016 Mar;11(4):554-64. doi: 10.1002/biot.201500159. Epub 2016 Jan 19.
The requirement for complex therapeutic proteins has resulted in mammalian cells, especially CHO cells, being the dominant host for recombinant protein manufacturing. In creating recombinant CHO cell lines, the expression vectors integrate into various parts of the genome leading to variable levels of expression and stability of protein production. This makes mammalian cell line development a long and laborious process. Therefore, with the intention to accelerate process development of recombinant protein production in CHO systems, UCOEs are utilized to diminish instability of production by maintaining an open chromatin surrounding in combination with MTX amplification. Chromosome painting and FISH analysis were performed to provide detailed molecular evaluation on the location of amplified genes and its relationship to the productivity and stability of the amplified cell lines. In summary, cell lines generated with vectors containing UCOEs retained stable GFP expression with MTX present (but instability was observed in the absence of MTX). UCOE cell lines displayed a higher frequency of integration into >1 chromosome than non-UCOE group. Cell populations were more homogenous in terms of transgene location at the end of Long-term culture (LTC). Overall our findings suggest variation in eGFP fluorescence may be attributed to changes in transgene integration profile over LTC.
对复杂治疗性蛋白质的需求导致哺乳动物细胞,尤其是CHO细胞,成为重组蛋白生产的主要宿主。在创建重组CHO细胞系时,表达载体整合到基因组的各个部分,导致蛋白质表达水平和生产稳定性各不相同。这使得哺乳动物细胞系的开发成为一个漫长而费力的过程。因此,为了加速CHO系统中重组蛋白生产的工艺开发,人们利用非编码上游调控元件(UCOEs)通过维持开放染色质环境并结合甲氨蝶呤(MTX)扩增来减少生产的不稳定性。进行了染色体描绘和荧光原位杂交(FISH)分析,以对扩增基因的位置及其与扩增细胞系的生产力和稳定性的关系提供详细的分子评估。总之,用含有UCOEs的载体产生的细胞系在存在MTX的情况下保持稳定的绿色荧光蛋白(GFP)表达(但在没有MTX的情况下观察到不稳定性)。与非UCOE组相比,UCOE细胞系整合到>1条染色体的频率更高。在长期培养(LTC)结束时,细胞群体在转基因位置方面更加均匀。总体而言,我们的研究结果表明,增强绿色荧光蛋白(eGFP)荧光的变化可能归因于长期培养过程中转基因整合谱的变化。