Satsu Hideo, Ishimoto Yoko, Nakano Tomoko, Mochizuki Tetsunosuke, Iwanaga Toshihiko, Shimizu Makoto
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Exp Cell Res. 2006 Nov 15;312(19):3909-19. doi: 10.1016/j.yexcr.2006.08.018. Epub 2006 Aug 30.
Intestinal epithelial cells interact with immune cells located in the intestinal epithelium via soluble factors. An in vitro model system using coculture was constructed to analyze the effect of macrophages on intestinal epithelial cells, and human intestinal epithelial-like Caco-2 monolayers and activated macrophage-like THP-1 cells were used in this study. Coculturing with THP-1 cells resulted in an increase of lactate dehydrogenase release from Caco-2 and a decrease in the transepithelial electrical resistance of the monolayers, showing that coculturing with THP-1 induced cell damage to Caco-2 cells. This disruption was significantly suppressed by adding anti-TNF-alpha antibody and etanercept, strongly suggesting that TNF-alpha secreted from THP-1 had caused cell damage to Caco-2 monolayers. The disrupted Caco-2 monolayers showed both apoptotic and necrotic characteristics by morphological and biochemical analyses. TNFRI and NF-kappaB seem to have been involved in this regulation. It is suggested that this phenomenon is similar in some respects to that observed with IBD and that this in vitro coculture system could be a good model for searching for the drugs or food substances that can be used to treat or prevent IBD.
肠道上皮细胞通过可溶性因子与位于肠道上皮中的免疫细胞相互作用。构建了一种使用共培养的体外模型系统来分析巨噬细胞对肠道上皮细胞的影响,本研究中使用了人肠道上皮样Caco-2单层细胞和活化的巨噬细胞样THP-1细胞。与THP-1细胞共培养导致Caco-2细胞中乳酸脱氢酶释放增加,单层细胞的跨上皮电阻降低,表明与THP-1共培养诱导了对Caco-2细胞的损伤。添加抗TNF-α抗体和依那西普可显著抑制这种破坏,强烈提示THP-1分泌的TNF-α对Caco-2单层细胞造成了损伤。通过形态学和生化分析,受损的Caco-2单层细胞表现出凋亡和坏死特征。TNFRI和NF-κB似乎参与了这一调节过程。提示这种现象在某些方面与炎症性肠病(IBD)中观察到的现象相似,并且这种体外共培养系统可能是寻找可用于治疗或预防IBD的药物或食物物质的良好模型。