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

机译:使用单细胞转录组学追踪克隆衍生的CHO细胞系中的生产不稳定

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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.
机译:各种机制包括转录沉默,基因拷贝丧失和对细胞应激的增加易感性已经与中国仓鼠卵巢(CHO)细胞系中单克隆抗体(MAB)生产的突然或逐渐丧失有关。在该研究中,我们利用单细胞RNA-SEQ(ScRNA-SEQ)研究克隆衍生的CHO细胞系,该CHO细胞系接受了产生的不稳定性,导致产生的MAb水平的显着降低。从ScRNA-SEQ数据中,我们鉴定了与MAB转基因的变化相关的亚型蛋白,并且观察到重链基因表达明显低于整个群体的轻链。使用轨迹推断,重建细胞系的演化,并发现与重链和轻链基因表达的减少相关。由于细胞沿着轨迹进展,发现编码参与氧化应激和细胞凋亡的响应和细胞凋亡的蛋白质的基因。使用这项技术的CHO细胞系的未来研究有可能大大提高我们对营养有效制造性能以及产品质量的特性的理解。

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