首页> 外文期刊>The British Journal of Nutrition >Transcriptional response of HT-29 intestinal epithelial cells to human and bovine milk oligosaccharides.
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Transcriptional response of HT-29 intestinal epithelial cells to human and bovine milk oligosaccharides.

机译:HT-29肠上皮细胞对人和牛乳寡糖的转录反应。

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Human milk oligosaccharides (HMO) have been shown to interact directly with immune cells. However, large quantities of HMO are required for intervention or clinical studies, but these are unavailable in most cases. In this respect, bovine milk is potentially an excellent source of commercially viable analogues of these unique molecules. In the present study, we compared the transcriptional response of colonic epithelial cells (HT-29) to the entire pool of HMO and bovine colostrum oligosaccharides (BCO) to determine whether the oligosaccharides from bovine milk had effects on gene expression that were similar to those of their human counterparts. Gene set enrichment analysis of the transcriptional data revealed that there were a number of similar biological processes that may be influenced by both treatments including a response to stimulus, signalling, locomotion, and multicellular, developmental and immune system processes. For a more detailed insight into the effects of milk oligosaccharides, the effect on the expression of immune system-associated glycogenes was chosen as a case study when performing validation studies. Glycogenes in the current context are genes that are directly or indirectly regulated in the presence of glycans and/or glycoconjugates. RT-PCR analysis revealed that HMO and BCO influenced the expression of cytokines (IL-1 beta, IL-8, colony-stimulating factor 2 (granulocyte-macrophage) (GM-CSF2), IL-17C and platelet factor 4 (PF4)), chemokines (chemokine (C-X-C motif) ligand 1 (CXCL1), chemokine (C-X-C motif) ligand 3 (CXCL3), chemokine (C-C motif) ligand 20 (CCL20), chemokine (C-X-C motif) ligand 2 (CXCL2), chemokine (C-X-C motif) ligand 6 (CXCL6), chemokine (C-C motif) ligand 5 (CCL5), chemokine (C-X3-C motif) ligand 1 (CX3CL1) and CXCL2) and cell surface receptors (interferon gamma receptor 1 (IFNGR1), intercellular adhesion molecule-1 (ICAM-1), intercellular adhesion molecule-2 (ICAM-2) and IL-10 receptor alpha (IL10RA)). The present study suggests that milk oligosaccharides contribute to the development and maturation of the intestinal immune response and that bovine milk may be an attractive commercially viable source of oligosaccharides for such applications
机译:人乳寡糖(HMO)已显示直接与免疫细胞相互作用。但是,干预或临床研究需要大量的HMO,但在大多数情况下这些是不可用的。在这方面,牛乳可能是这些独特分子的商业上可行的类似物的极佳来源。在本研究中,我们比较了结肠上皮细胞(HT-29)对整个HMO和牛初乳寡糖(BCO)的转录反应,以确定牛乳中的寡糖是否对基因表达有类似的影响。他们的人类同行。转录数据的基因集富集分析表明,两种处理都可能影响许多相似的生物学过程,包括对刺激,信号传导,运动以及多细胞,发育和免疫系统过程的反应。为了更深入地了解牛奶寡糖的影响,在进行验证研究时,选择对免疫系统相关糖基因表达的影响作为案例研究。当前上下文中的糖原基因是在聚糖和/或糖缀合物的存在下直接或间接调节的基因。 RT-PCR分析显示HMO和BCO影响细胞因子(IL-1 beta,IL-8,集落刺激因子2(粒细胞巨噬细胞)(GM-CSF2),IL-17C和血小板因子4(PF4)的表达),趋化因子(趋化因子(CXC主题)配体1(CXCL1),趋化因子(CXC主题)配体3(CXCL3),趋化因子(CC主题)配体20(CCL20),趋化因子(CXC主题)配体2(CXCL2),趋化因子( CXC基序)配体6(CXCL6),趋化因子(CC基序)配体5(CCL5),趋化因子(C-X3-C基序)配体1(CX3CL1)和CXCL2)和细胞表面受体(干扰素γ受体1(IFNGR1),细胞间粘附分子-1(ICAM-1),细胞间粘附分子2(ICAM-2)和IL-10受体α(IL10RA)。本研究表明,牛奶中的低聚糖有助于肠道免疫反应的发展和成熟,牛乳可能是此类应用中商业上有吸引力的低聚糖来源

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