Role of Toll Like Receptors in Irritable Bowel Syndrome: Differential Mucosal Immune Activation According to the Disease Subtype

被引:104
作者
Belmonte, Liliana [1 ,2 ,3 ]
Youmba, Stephanie Beutheu [1 ,2 ]
Bertiaux-Vandaele, Nathalie [4 ]
Antonietti, Michel [4 ]
Lecleire, Stephane [1 ,2 ,4 ]
Zalar, Alberto [4 ]
Gourcerol, Guillaume [1 ,2 ,5 ]
Leroi, Anne-Marie [1 ,2 ,5 ]
Dechelotte, Pierre [1 ,2 ,6 ]
Coeffier, Moise [1 ,2 ,6 ]
Ducrotte, Philippe [1 ,2 ,4 ]
机构
[1] Univ Rouen, INSERM, U1073, Rouen, France
[2] Univ Rouen, Inst Res & Innovat Biomed, Rouen, France
[3] Natl Acad Med Buenos Aires, Consejo Nacl Invest Cient & Tecn, Immunol Lab, IIHema, Buenos Aires, DF, Argentina
[4] Rouen Univ Hosp, Dept Gastroenterol, Rouen, France
[5] Rouen Univ Hosp, Dept Physiol, Rouen, France
[6] Rouen Univ Hosp, Nutr Unit, Rouen, France
关键词
INTESTINAL PERMEABILITY; EXPRESSION; TLR4; GUT; RECOGNITION; ASSOCIATION; GLUTAMINE; GAMMA;
D O I
10.1371/journal.pone.0042777
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: The irritable bowel syndrome (IBS) is a functional gastrointestinal disorder whose pathogenesis is not completely understood. Its high prevalence and the considerable effects on quality of life make IBS a disease with high social cost. Recent studies suggest that low grade mucosal immune activation, increased intestinal permeability and the altered host-microbiota interactions that modulate innate immune response, contribute to the pathophysiology of IBS. However, the understanding of the precise molecular pathophysiology remains largely unknown. Methodology and Findings: In this study our objective was to evaluate the TLR expression as a key player in the innate immune response, in the colonic mucosa of IBS patients classified into the three main subtypes (with constipation, with diarrhea or mixed). TLR2 and TLR4 mRNA expression was assessed by real time RT-PCR while TLRs protein expression in intestinal epithelial cells was specifically assessed by flow cytometry and immunofluorescence. Mucosal inflammatory cytokine production was investigated by the multiplex technology. Here we report that the IBS-Mixed subgroup displayed a significant up-regulation of TLR2 and TLR4 in the colonic mucosa. Furthermore, these expressions were localized in the epithelial cells, opening new perspectives for a potential role of epithelial cells in host-immune interactions in IBS. In addition, the increased TLR expression in IBS-M patients elicited intracellular signaling pathways resulting in increased expression of the mucosal proinflammatory cytokines IL-8 and IL1 beta. Conclusions: Our results provide the first evidence of differential expression of TLR in IBS patients according to the disease subtype. These results offer further support that microflora plays a central role in the complex pathophysiology of IBS providing novel pharmacological targets for this chronic gastrointestinal disorder according to bowel habits.
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页数:10
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