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Gene expression profiles in human peripheral blood mononuclear cells as biomarkers for nutritional in vitro and in vivo investigations

机译:人类外周血单核细胞中的基因表达谱作为生物标记的营养性体内外研究

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摘要

Identification of chemopreventive substances may be achieved by measuring biological endpoints in human cells in vitro. Since generally only tumour cells are available for such investigations, our aim was to test the applicability of peripheral blood mononuclear cells (PBMC) as an in vitro primary cell model since they mimic the human in vivo situation and are relatively easily available. Cell culture conditions were refined, and the basal variation of gene expression related to drug metabolism and stress response was determined. Results were compared with profiles of an established human colon cell line (HT29) as standard. For biomarker development of nutritional effects, PBMC and HT29 cells were treated with potentially chemopreventive substances (chrysin and butyrate), and gene expression was determined. Key results were that relevant stress response genes, such as glutathione S-transferase T2 (GSTT2) and GSTM2, were modulated by butyrate in PBMC as in HT29 cells, but the blood cells were less sensitive and responded with high individual differences. We conclude that these cells may serve as a surrogate tissue in dietary investigations and the identified differentially expressed genes have the potential to become marker genes for population studies on biological effects.
机译:化学预防物质的鉴定可以通过在体外测量人细胞中的生物学终点来实现。由于通常只有肿瘤细胞可用于此类研究,因此我们的目标是测试外周血单核细胞(PBMC)作为体外原代细胞模型的适用性,因为它们可模拟人体内情况并且相对容易获得。完善细胞培养条件,并确定与药物代谢和应激反应相关的基因表达的基础变化。将结果与已建立的人结肠细胞系(HT29)的谱图进行比较。为了开发营养作用的生物标志物,将PBMC和HT29细胞用潜在的化学预防物质(胰蛋白酶和丁酸)处理,并确定基因表达。关键结果是,与HT29细胞一样,PBMC中的丁酸盐调节了相关的应激反应基因,如谷胱甘肽S-转移酶T2(GSTT2)和GSTM2,但血细胞敏感度较低,并具有较高的个体差异。我们得出的结论是,这些细胞可能在饮食研究中充当替代组织,并且所鉴定的差异表达基因有可能成为生物学研究人群研究的标记基因。

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