Immunologic regulation of toll-like receptors in gut epithelium

被引:34
作者
Abreu, MT [1 ]
机构
[1] Cedars Sinai Med Ctr, Ctr Inflammatory Bowel Dis, Burns & Allen Res Inst, Dept Med,Div Gastroenterol, Los Angeles, CA 90048 USA
关键词
innate immunity; NF-kappa B; lipopolysaccharide; toll-like receptors; inflammatory bowel disease; NOD1; NOD2;
D O I
10.1097/00001574-200311000-00008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review In response to the presence of pathogens in the environment, the innate immune system has evolved to provide a rapid defense against microbes. This response involves the recognition of molecular patterns present in diverse microbes by a series of receptors termed toll-like receptors. The focus of this article is the regulation of toll-like receptor signaling in the intestinal epithelium. The intestinal epithelium is continually exposed to a high concentration of diverse bacteria. In spite of the density of commensal bacteria, the normal intestine is not inflamed. Idiopathic inflammatory bowel disease in humans and animals is characterized by aberrant host-microbial interactions. Recent findings Several studies demonstrate that intestinal epithelial cells are poorly responsive to microbial products. The reason for this hyporesponsiveness is decreased or polarized expression of toll-like receptor molecules. Inflammatory cytokines upregulate expression of toll-like receptors. Summary The intestinal epithelium has evolved under the pressure of the microbiota to mute a response to commensal bacteria while maintaining the ability to respond to pathogens. In inflammatory bowel disease, the loss of tolerance to the normal flora may be due in part to inappropriate toll-like receptor signaling.
引用
收藏
页码:559 / 564
页数:6
相关论文
共 54 条
[1]   TLR4 and MD-2 expression is regulated by immune-mediated signals in human intestinal epithelial cells [J].
Abreu, MT ;
Arnold, ET ;
Thomas, LS ;
Gonsky, R ;
Zhou, YH ;
Hu, B ;
Arditi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20431-20437
[2]   Decreased expression of toll-like receptor-4 and MD-2 correlates with intestinal epithelial cell protection against dysregulated proinflammatory gene expression in response to bacterial lipopolysaccharide [J].
Abreu, MT ;
Vora, P ;
Faure, E ;
Thomas, LS ;
Arnold, ET ;
Arditi, M .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1609-1616
[3]   Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease [J].
Abreu, MT ;
Taylor, KD ;
Lin, YC ;
Hang, T ;
Gaiennie, J ;
Landers, CJ ;
Vasiliauskas, EA ;
Kam, LY ;
Rojany, M ;
Papadakis, KA ;
Rotter, JI ;
Targan, SR ;
Yang, HY .
GASTROENTEROLOGY, 2002, 123 (03) :679-688
[4]   Bacterial DNA evokes epithelial IL-8 production by a MAPK-dependent, NFκB-independent pathway [J].
Akhtar, M ;
Watson, JL ;
Nazli, A ;
McKay, DM .
FASEB JOURNAL, 2003, 17 (08) :1319-+
[5]   Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[6]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[7]   Role of EHEC O157:H7 virulence factors in the activation of intestinal epithelial cell NF-κB and MAP kinase pathways and the upregulated expression of interleukin 8 [J].
Berin, MC ;
Darfeuille-Michaud, A ;
Egan, LJ ;
Miyamoto, Y ;
Kagnoff, MF .
CELLULAR MICROBIOLOGY, 2002, 4 (10) :635-647
[8]   Card15 gene overexpression in mononuclear and epithelial cells of the inflamed Crohn's disease colon [J].
Berrebi, D ;
Maudinas, R ;
Hugot, JP ;
Chamaillard, M ;
Chareyre, F ;
De Lagausie, P ;
Yang, C ;
Desreumaux, P ;
Giovannini, M ;
Cézard, JP ;
Zouali, H ;
Emilie, D ;
Peuchmaur, M .
GUT, 2003, 52 (06) :840-846
[9]   Regulatory T cells selectively express toll-like receptors and are activated by lipopolysaccharide [J].
Caramalho, I ;
Lopes-Carvalho, T ;
Ostler, D ;
Zelenay, S ;
Haury, M ;
Demengeot, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (04) :403-411
[10]   Differential alteration in intestinal epithelial cell expression of Toll-like receptor 3 (TLR3) and TLR4 in inflammatory bowel disease [J].
Cario, E ;
Podolsky, DK .
INFECTION AND IMMUNITY, 2000, 68 (12) :7010-7017