首页> 外文期刊>Biotechnology Journal: Healthcare,Nutrition,Technology >Microarray expression profiling identifies genes regulating sustained cell specific productivity (S-Qp) in CHO K1 production cell lines
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Microarray expression profiling identifies genes regulating sustained cell specific productivity (S-Qp) in CHO K1 production cell lines

机译:芯片表达谱分析鉴定了调节CHO K1生产细胞系中持续细胞比生产率(S-Qp)的基因

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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 MCST1) both replicated the microarray results and were differentially regulated between the NS and S phenotypes.
机译:补料分批培养过程的特征通常是随着过程的进行而降低细胞培养性能,大概是由于重要营养物质的消耗和有毒副产物的积累。我们类似地观察到,在分批补料过程中,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引发这种行为,而另一些则不会。我们在这里提供了生产的中国仓鼠卵巢(CHO)培养物中持续Qp(S-Qp)表型的转录组分析,其中两个细胞中Qp水平显着下降(“非持续”(NS)表型)将不考虑存活水平的细胞系与在整个培养中始终显示出高Qp的两个细胞系(“持续”(S)表型)进行比较。对微阵列数据的统计分析导致鉴定出22个基因转录物,其表达模式在培养寿命内与Qp的长期维持呈显着负相关或正相关。通过微阵列分析对每个细胞系(NS2,S2)中的一个基因的四个基因进行qPCR分析,证实两个基因(CRYAB和MCST1)复制了微阵列结果,并且在NS和S表型之间受到差异调节。

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