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微阵列表达谱分析鉴定了调控 CHO K1 生产细胞系中持续细胞特异性生产率(S-Qp)的基因。

Microarray expression profiling identifies genes regulating sustained cell specific productivity (S-Qp) in CHO K1 production cell lines.

机构信息

National Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.

出版信息

Biotechnol J. 2012 Apr;7(4):516-26. doi: 10.1002/biot.201100255. Epub 2012 Jan 18.

Abstract

Fed batch culture processes are often characterized by decreasing cell culture performance as the process continues, presumably through the depletion of vital nutrients and the accumulation of toxic byproducts. We have similarly observed that cellular productivity (Qp) often declines during the course of a fed batch process; however, it is not clear why some cell lines elicit this behavior, while others do not. We here present a transcriptomic profiling analysis of a phenotype of sustained Qp (S-Qp) in production Chinese hamster ovary (CHO) culture, in which a marked drop in Qp levels ("non-sustained" (NS) phenotype) in two cell lines irrespective of viability levels was compared to two cell lines that consistently displayed high Qp throughout the culture ("sustained" (S) phenotype). Statistical analysis of the microarray data resulted in the identification of 22 gene transcripts whose expression patterns were either significantly negatively or positively correlated with long-term maintenance of Qp over the culture lifespan. qPCR analysis of four of these genes on one of each (NS2, S2) of the cell lines examined by microarray analysis confirmed that two genes (CRYAB and MGST1) both replicated the microarray results and were differentially regulated between the NS and S phenotypes.

摘要

补料分批培养过程通常表现为随着培养过程的进行,细胞培养性能逐渐下降,推测是由于重要营养物质的耗尽和有毒副产物的积累。我们同样观察到,在补料分批过程中,细胞生产率(Qp)通常会下降;然而,尚不清楚为什么有些细胞系会表现出这种行为,而有些则不会。在这里,我们对生产中国仓鼠卵巢(CHO)培养中持续 Qp(S-Qp)的表型进行了转录组谱分析,其中两个细胞系的 Qp 水平明显下降(“非持续”(NS)表型),而与两个细胞系的活力水平无关,而两个细胞系在整个培养过程中始终表现出高 Qp(“持续”(S)表型)。对微阵列数据的统计分析导致鉴定出 22 个基因转录本,其表达模式与 Qp 在培养寿命内的长期维持呈显著负相关或正相关。对微阵列分析检查的细胞系中的四个基因中的四个基因进行 qPCR 分析证实,两个基因(CRYAB 和 MGST1)均复制了微阵列结果,并在 NS 和 S 表型之间存在差异调节。

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