Transcriptomic response of immune signalling pathways in intestinal epithelial cells exposed to lipopolysaccharides, Gram-negative bacteria or potentially probiotic microbes

被引:19
作者
Audy, J. [1 ,2 ]
Mathieu, O. [1 ]
Belvis, J. [1 ]
Tompkins, T. A. [1 ]
机构
[1] Lallemand Human Nutr, Montreal, PQ H4P 2R2, Canada
[2] Agropur Cooperat, St Hubert, PQ J3Z 1G5, Canada
关键词
microarray; transcriptomic; immunity; MAP kinase; TOLL-LIKE RECEPTORS; ESCHERICHIA-COLI; GENE-EXPRESSION; FUNCTIONAL MODULATION; NISSLE; 1917; LACTOBACILLUS; COMMENSAL; ADHESION; CHEMOKINE; PCR;
D O I
10.3920/BM2012.0027
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In order to understand the appropriate use of potentially probiotic Gram-positive microbes through their introduction in the gut microbiome, it is necessary to understand the influence of individual bacteria on the host-response system at a cellular level. In the present study, we have shown that lipopolysaccharides, flagellated Gram-negative bacteria, potentially probiotic Gram-positive bacteria and yeast interact differently with human intestinal epithelial cells with a custom-designed expression microarray evaluating 17 specific host-response pathways. Only lipopolysaccharides and flagellated Gram-negative bacteria induced inflammatory response, while a subset of Gram-positive microbes had anti-inflammatory potential. The main outcome from the study was the differential regulation of the central mitogen-activated protein kinase signalling pathway by these Gram-positive microbes versus commensal/pathogenic Gram-negative bacteria. The microarray was efficient to highlight the impact of individual bacteria on the response of intestinal epithelial cells, but quantitative real-time polymerase chain reaction validation demonstrated some underestimation for down-regulated genes by the microarray. This immune array will allow us to better understand the mechanisms underlying microbe-induced host immune responses.
引用
收藏
页码:273 / 286
页数:14
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