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Transgene copy number distribution profiles in recombinant CHO cell lines revealed by single cell analyses

机译:单细胞分析揭示重组CHO细胞系中的转基因拷贝数分布图

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摘要

Clonally derived recombinant cell lines are highly desired to achieve consistent production of recombinant biotherapeutics. Despite repeated rounds of cloning by limiting dilution or single cell cloning, the resulting cell lines have often been observed to diverge, becoming a heterogeneous population and losing productivity over long-term sub-culturing. To understand the underlying molecular mechanisms, we developed quantitative polymerase chain reaction (qPCR) assays for the analysis of transgene copy number distribution in single recombinant cells isolated from Chinese hamster ovary (CHO) cell lines. Single cells were obtained by fluorescence activated cell sorting (FACS) technology and lysed directly in 96-well plates. qPCR assays were then applied to analyze the quantity and distribution of transgenes in those single cells. Results revealed multiple types of transgene copy number distribution profiles from those clonally derived CHO cell lines. The cell lines that maintained productivity over time displayed relatively constant and homogeneous transgene copy number distributions; while most of those cell lines exhibiting a loss of productivity over time showed varying degrees of transgene copy number heterogeneity and distribution drift with passaging. Some cell lines showed the existence of a significant portion of cells lacking the transgenes (referred to as negative cells in this study) and the percentage of those negative cells increased with subsequent generations. Criteria based on transgene copy number distribution profiles were developed to assess cell line suitability for clinical applications, which include (i) percentage of negative cells; (ii) standard deviation of qPCR threshold cycle (C _t) value, a measure of population heterogeneity; (iii) mean C _t changes during aging, a measure of population drift. By implementing these criteria, undesirable cell lines were eliminated for further clinical and commercial applications.
机译:为了实现一致的重组生物治疗药物的生产,非常需要克隆衍生的重组细胞系。尽管通过有限稀释或单细胞克隆重复进行了几轮克隆,但经常观察到所得细胞系发生分化,成为异质群体,并在长期传代培养中丧失生产力。为了解潜在的分子机制,我们开发了定量聚合酶链反应(qPCR)分析方法,用于分析从中国仓鼠卵巢(CHO)细胞系中分离的单个重组细胞中的转基因拷贝数分布。通过荧光激活细胞分选(FACS)技术获得单细胞,并直接在96孔板中裂解。然后将qPCR分析应用于分析那些单细胞中转基因的数量和分布。结果揭示了来自那些克隆衍生的CHO细胞系的多种类型的转基因拷贝数分布图。随着时间的推移保持生产力的细胞系显示出相对恒定和均一的转基因拷贝数分布。而随着时间的流逝,大多数表现出生产力下降的细胞系表现出不同程度的转基因拷贝数异质性以及随着传代而发生的分布漂移。一些细胞系显示存在大量缺少转基因的细胞(在本研究中称为阴性细胞),并且这些阴性细胞的百分比随后代而增加。制定了基于转基因拷贝数分布概况的标准,以评估细胞系对临床应用的适用性,其中包括:(i)阴性细胞的百分比; (ii)qPCR阈值循环(C _t)值的标准差,该标准差是群体异质性的量度; (iii)平均C _t在衰老过程中的变化,是人口漂移的量度。通过实施这些标准,消除了不良的细胞系,以用于进一步的临床和商业应用。

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