Huang Zicheng, Shao Wei, Gu Jinping, Hu Xiaomin, Shi Yuanzhi, Xu Wenqi, Huang Caihua, Lin Donghai
High-field NMR Research Center, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China.
Mol Biosyst. 2015 Jul;11(7):1832-40. doi: 10.1039/c5mb00019j.
Cell culture metabolomics has demonstrated significant advantages in cancer research. However, its applications have been impeded by some influencing factors such as culture media, which could significantly affect cellular metabolic profiles and lead to inaccuracy and unreliability of comparative metabolomic analysis of cells. To evaluate the effects of different culture media on cellular metabolic profiling, we performed NMR-based metabolomic analysis of the human gastric cancer cell line SGC7901 cultured in both RPMI1640 and DMEM. We found that SGC7901 cultured in the two media exhibited distinct metabolic profiles with obviously different levels of discrepant metabolites, even though they showed almost the same cellular morphology and proliferation rates. When SGC7901 originally cultured in RPMI1640 was gradually acclimated in DMEM, both the metabolic profiles and most of the discrepant metabolite levels gradually converged toward those of the cells originally cultured in DMEM without significantly altered cell proliferation rates. However, several metabolite levels did not show the converging trends. Our results indicate that the effects of culture media on metabolic profiling must be carefully taken into account for comparative metabolomic analysis of cell lines. This work may be of benefit to the development of cell culture metabolomics.
细胞培养代谢组学在癌症研究中已展现出显著优势。然而,其应用受到一些影响因素的阻碍,比如培养基,它会显著影响细胞代谢谱,导致细胞比较代谢组学分析的不准确和不可靠。为评估不同培养基对细胞代谢谱的影响,我们对在RPMI1640和DMEM中培养的人胃癌细胞系SGC7901进行了基于核磁共振的代谢组学分析。我们发现,在这两种培养基中培养的SGC7901呈现出不同的代谢谱,差异代谢物水平明显不同,尽管它们的细胞形态和增殖速率几乎相同。当原本在RPMI1640中培养的SGC7901逐渐适应DMEM时,代谢谱和大多数差异代谢物水平都逐渐向原本在DMEM中培养的细胞靠拢,且细胞增殖速率没有显著改变。然而,有几种代谢物水平并未呈现出趋同趋势。我们的结果表明,在对细胞系进行比较代谢组学分析时,必须仔细考虑培养基对代谢谱的影响。这项工作可能有助于细胞培养代谢组学的发展。