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Development of the method for evaluating protective effect of food factors on THP-1-induced damage to human intestinal Caco-2 monolayers

机译:用于评估食物因素对人肠道Caco-2单层损伤的保护作用的方法

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Immune cells located in the intestinal epithelium interact with intestinal epithelial cells via soluble factors. In this study, a new in vitro model using a coculture system was constructed to analyze the interaction between intestinal epithelial cells and macrophage-like cells. Human intestinal epithelial Caco-2 cells were differentiated on semipermeable membranes. Human monocytic THP-1 cells were differentiated to macrophage-like cells and then cocultured on the basolateral side of the Caco-2 cell monolayers. By coculturing for 48 hours, an increased release of lactate dehydrogenase from the Caco-2 cells and a decrease in the transepithelial electrical resistance of the monolayers were observed, suggesting that the coculture with THP-1 induced some disruption of the Caco-2 cells. This disruption was significantly suppressed by adding the anti-TNF-α antibody to the medium, suggesting that TNF-α secreted from THP-1 caused damage to the Caco-2 cells. It is also suggested that this phenomenon is similar to that observed with inflammatory bowel disease (IBD). The effects of food factors on the cells in this coculture system were examined. The disruption of the Caco-2 cell monolayers was significantly reduced by adding caffeine to the medium on the apical side. It is hoped that this coculture system will be a good model for the treatment of IBD.
机译:位于肠上皮的免疫细胞通过可溶性因子与肠上皮细胞相互作用。在该研究中,建立了使用共培养系统的新体外模型,以分析肠上皮细胞和巨噬细胞样细胞之间的相互作用。人肠上皮CaCo-2细胞在半透明膜上分化。人单核细胞THP-1细胞与巨噬细胞样细胞分化,然后在CaCo-2细胞单层的基底外侧携带。通过共培养48小时,观察到从CaCO-2细胞释放乳酸脱氢酶的释放和单层的培养型电阻的降低,表明与THP-1的共络诱导了CACO-2细胞的一些破坏。通过向培养基添加抗TNF-α抗体来显着抑制这种破坏,表明从THP-1分泌的TNF-α导致CACO-2细胞损伤。还建议这种现象类似于炎症性肠病(IBD)观察到的现象。检查了食品因素对该共培养系统中细胞的影响。通过将咖啡因添加到顶端侧的培养基中,显着降低了Caco-2细胞单层的破坏。希望这个共科养殖系统将是治疗IBD的良好模型。

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