Tracing production instability in a clonally derived CHO cell line using single-cell transcriptomics

被引:16
|
作者
Tzani, Ioanna [1 ]
Herrmann, Nicolas [2 ]
Carillo, Sara [1 ]
Spargo, Cathy A. [2 ]
Hagan, Ryan [1 ,3 ]
Barron, Niall [1 ,3 ]
Bones, Jonathan [1 ,3 ]
Shannon Dillmore, W. [2 ]
Clarke, Colin [1 ,3 ]
机构
[1] Natl Inst Bioproc Res & Training, Fosters Ave, Blackrock A94 X099, Dublin, Ireland
[2] BD Technol & Innovat, Res Triangle Pk, NC USA
[3] Univ Coll Dublin, Sch Chem & Bioproc Engn, Dublin, Ireland
基金
爱尔兰科学基金会; 欧盟地平线“2020”;
关键词
Chinese hamster ovary; heterogeneity; next‐ generation sequencing; single‐ cell RNA‐ seq; transcriptomics; MASS-SPECTROMETRY; OXIDATIVE STRESS; SEQUENCE; HETEROGENEITY; GENOME;
D O I
10.1002/bit.27715
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A variety of mechanisms including transcriptional silencing, gene copy loss, and increased susceptibility to cellular stress have been associated with a sudden or gradual loss of monoclonal antibody (mAb) production in Chinese hamster ovary (CHO) cell lines. In this study, we utilized single-cell RNA-seq (scRNA-seq) to study a clonally derived CHO cell line that underwent production instability leading to a dramatic reduction of the levels of mAb produced. From the scRNA-seq data, we identified subclusters associated with variations in the mAb transgenes and observed that heavy chain gene expression was significantly lower than that of the light chain across the population. Using trajectory inference, the evolution of the cell line was reconstructed and was found to correlate with a reduction in heavy and light chain gene expression. Genes encoding for proteins involved in the response to oxidative stress and apoptosis were found to increase in expression as cells progressed along the trajectory. Future studies of CHO cell lines using this technology have the potential to dramatically enhance our understanding of the characteristics underpinning efficient manufacturing performance as well as product quality.
引用
收藏
页码:2016 / 2030
页数:15
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