碳酸钙-2
生物
肿瘤坏死因子α
细胞凋亡
肠上皮
细胞生物学
免疫系统
乳酸脱氢酶
上皮
体外
细胞
巨噬细胞
细胞培养
肠粘膜
分子生物学
免疫学
生物化学
酶
内科学
医学
遗传学
作者
Hideo Satsu,Yoko Ishimoto,Tomoko Nakano,Tetsunosuke Mochizuki,Toshihiko Iwanaga,Makoto Shimizu
标识
DOI:10.1016/j.yexcr.2006.08.018
摘要
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.
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