势垒函数
分泌物
生物
免疫系统
丁酸盐
肿瘤坏死因子α
微生物学
白细胞介素
促炎细胞因子
白细胞介素8
肠上皮
细胞因子
戊酸盐
体外
上皮
炎症
免疫学
生物化学
细胞生物学
发酵
遗传学
作者
Marleen H.M.C. van Nuenen,Rianne A.F. de Ligt,Robert Doornbos,Janneke C. J. Van Der Woude,Ernst J. Kuipers,Koen Venema
出处
期刊:Fems Immunology and Medical Microbiology
[Oxford University Press]
日期:2005-08-01
卷期号:45 (2): 183-189
被引量:43
标识
DOI:10.1016/j.femsim.2005.03.010
摘要
Microbial metabolites may influence the metabolic integrity of intestinal epithelial cells and induce mucosal immune responses. Therefore, we investigated the effects of the microbial metabolites butyrate, iso-valerate, and ammonium on Caco-2 cells and macrophages. Barrier functioning was determined by measuring transepithelial electrical resistance and basolateral recoveries of metabolites. The barrier function of Caco-2 cells remained intact after exposures. Basolateral recoveries ranged from 6.2% to 15.2%. Tumour necrosis factor-alpha and interleukin-10 were measured to determine immune reactions. The Caco-2 cells did not secrete both cytokines. Physiological concentrations of butyrate and iso-valerate stimulated the secretion of tumour necrosis factor-alpha and suppressed the secretion of interleukin-10 by macrophages that are not protected by an epithelial barrier. In contrast, ammonium concentrations as high as those produced by microbiotas of IBD patients suppressed the release of both cytokines when the barrier function is impaired.
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