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1H NMR Spectroscopy Profiling of Metabolic Reprogramming of Chinese Hamster Ovary Cells upon a Temperature Shift during Culture

机译:1H NMR谱分析在培养过程中温度变化后中国仓鼠卵巢细胞的代谢重编程

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摘要

We report an NMR based approach to determine the metabolic reprogramming of Chinese hamster ovary cells upon a temperature shift during culture by investigating the extracellular cell culture media and intracellular metabolome of CHOK1 and CHO-S cells during culture and in response to cold-shock and subsequent recovery from hypothermic culturing. A total of 24 components were identified for CHOK1 and 29 components identified for CHO-S cell systems including the observation that CHO-S media contains 5.6 times the level of glucose of CHOK1 media at time zero. We confirm that an NMR metabolic approach provides quantitative analysis of components such as glucose and alanine with both cell lines responding in a similar manner and comparable to previously reported data. However, analysis of lactate confirms a differentiation between CHOK1 and CHO-S and that reprogramming of metabolism in response to temperature was cell line specific. The significance of our results is presented using principal component analysis (PCA) that confirms changes in metabolite profile in response to temperature and recovery. Ultimately, our approach demonstrates the capability of NMR providing real-time analysis to detect reprogramming of metabolism upon cellular perception of cold-shock/sub-physiological temperatures. This has the potential to allow manipulation of metabolites in culture supernatant to improve growth or productivity.
机译:我们报告了一种基于核磁共振的方法,通过研究培养过程中对CHOK1和CHO-S细胞的细胞外细胞培养基和细胞内代谢物以及对冷休克和随后反应的反应,来确定培养过程中温度变化后中国仓鼠卵巢细胞的代谢重编程从低温培养中恢复。共确定了CHOK1的24种成分,并为CHO-S细胞系统鉴定了29种成分,包括观察到CHO-S培养基在零时点所含葡萄糖含量是CHOK1培养基的5.6倍。我们确认,NMR代谢方法可以定量分析诸如葡萄糖和丙氨酸之类的成分,并且两种细胞系都以相似的方式响应,并且可以与先前报道的数据进行比较。但是,乳酸分析证实了CHOK1和CHO-S之间的差异,并且响应温度的代谢重编程是细胞系特异性的。使用主成分分析(PCA)展示了我们研究结果的意义,该分析确认了代谢物谱随温度和回收率的变化。最终,我们的方法证明了NMR能够提供实时分析功能,以在细胞感知到冷休克/亚生理温度时检测新陈代谢的重编程。这具有允许操纵培养物上清液中的代谢物以改善生长或生产率的潜力。

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