Toll-Like Receptor-Gut Microbiota Interactions: Perturb at Your Own Risk!

被引:118
作者
Carvalho, Frederic A. [1 ,2 ]
Aitken, Jesse D. [3 ]
Vijay-Kumar, Matam [3 ]
Gewirtz, Andrew T. [3 ]
机构
[1] Univ Auvergne, Clermont Univ, Clin Douleur, F-63000 Clermont Ferrand, France
[2] INSERM, U766, F-63001 Clermont Ferrand, France
[3] Georgia State Univ, Ctr Inflammat Immun & Infect, Dept Biol, Atlanta, GA 30303 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 74 | 2012年 / 74卷
关键词
inflammatory bowel disease; cancer; metabolic syndrome; MyD88; intestinal homeostasis; INTESTINAL MICROBIOTA; INNATE IMMUNITY; CROHNS-DISEASE; SEROVAR TYPHIMURIUM; ULCERATIVE-COLITIS; COMMENSAL BACTERIA; ADAPTIVE IMMUNITY; COLORECTAL-CANCER; EPITHELIAL-CELLS; MURINE MODEL;
D O I
10.1146/annurev-physiol-020911-153330
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The well-being of the intestine and its host requires that this organ execute its complex function amid colonization by a large and diverse microbial community referred to as the gut microbiota. A myriad of interacting mechanisms of mucosal immunity permit the gut to corral the microbiota in such a way as to maximize the benefits and to minimize the danger of living in close proximity to this large microbial biomass. Toll-like receptors and Nod-like receptors, collectively referred to as pattern recognition receptors (PRRs), recognize a variety of microbial components and, hence, play a central role in governing the interface between host and microbiota. This review examines mechanisms by which PRR-microbiota interactions are regulated so as to allow activation of host defense when necessary while preventing excessive inflammation, which can have a myriad of negative consequences for the host. Analysis of published studies performed in human subjects and a variety of murine disease models reveals the central theme that PRRs play a key role in maintaining a healthful stable relationship between the intestine and its microbiota. In contrast, although select genetic ablations of PRR signaling may protect against some chronic diseases, the overriding theme of studies performed to date is that perturbations of PRR-microbiota interactions are more likely to promote disease states associated with inflammation.
引用
收藏
页码:177 / 198
页数:22
相关论文
共 123 条
[1]  
ABRAMS GD, 1963, LAB INVEST, V12, P355
[2]   Lactic acid permeabilizes gram-negative bacteria by disrupting the outer membrane [J].
Alakomi, HL ;
Skyttä, E ;
Saarela, M ;
Mattila-Sandholm, T ;
Latva-Kala, K ;
Helander, IM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (05) :2001-2005
[3]   The NLRP3 inflammasome functions as a negative regulator of tumorigenesis during colitis-associated cancer [J].
Allen, Irving C. ;
TeKippe, Erin McElvania ;
Woodford, Rita-Marie T. ;
Uronis, Joshua M. ;
Holl, Eda K. ;
Rogers, Arlin B. ;
Herfarth, Hans H. ;
Jobin, Christian ;
Ting, Jenny P. -Y. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2010, 207 (05) :1045-1056
[4]   Pathogenic and Protective Roles of MyD88 in Leukocytes and Epithelial Cells in Mouse Models of Inflammatory Bowel Disease [J].
Asquith, Mark J. ;
Boulard, Olivier ;
Powrie, Fiona ;
Maloy, Kevin J. .
GASTROENTEROLOGY, 2010, 139 (02) :519-529
[5]   Mucosal Lipocalin 2 Has Pro-Inflammatory and Iron-Sequestering Effects in Response to Bacterial Enterobactin [J].
Bachman, Michael A. ;
Miller, Virginia L. ;
Weiser, Jeffrey N. .
PLOS PATHOGENS, 2009, 5 (10)
[6]   CEACAM6 acts as a receptor for adherent-invasive E. coli, supporting ileal mucosa colonization in Crohn disease [J].
Barnich, Nicolas ;
Carvalho, Frederic A. ;
Glasser, Anne-Lise ;
Darcha, Claude ;
Jantscheff, Peter ;
Allez, Matthieu ;
Peeters, Harald ;
Bommelaer, Gilles ;
Desreumaux, Pierre ;
Colombel, Jean-Frederic ;
Darfeuille-Michaud, Arlette .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (06) :1566-1574
[7]   Colitis induced in mice with dextran sulfate sodium (DSS) is mediated by the NLRP3 inflammasome [J].
Bauer, Christian ;
Duewell, Peter ;
Mayer, Christine ;
Lehr, Hans Anton ;
Fitzgerald, Katherine A. ;
Dauer, Marc ;
Tschopp, Jurg ;
Endres, Stefan ;
Latz, Eicke ;
Schnurr, Max .
GUT, 2010, 59 (09) :1192-1199
[8]   Muc2 Protects against Lethal Infectious Colitis by Disassociating Pathogenic and Commensal Bacteria from the Colonic Mucosa [J].
Bergstrom, Kirk S. B. ;
Kissoon-Singh, Vanessa ;
Gibson, Deanna L. ;
Ma, Caixia ;
Montero, Marinieve ;
Sham, Ho Pan ;
Ryz, Natasha ;
Huang, Tina ;
Velcich, Anna ;
Finlay, B. Brett ;
Chadee, Kris ;
Vallance, Bruce A. .
PLOS PATHOGENS, 2010, 6 (05)
[9]   Endotoxin tolerance: new mechanisms, molecules and clinical significance [J].
Biswas, Subhra K. ;
Lopez-Collazo, Eduardo .
TRENDS IN IMMUNOLOGY, 2009, 30 (10) :475-487
[10]   Myd88-dependent positioning of Ptgs2-expressing stromal cells maintains colonic epithelial proliferation during injury [J].
Brown, Sarah L. ;
Riehl, Terrence E. ;
Walker, Monica R. ;
Geske, Michael J. ;
Doherty, Jason M. ;
Stenson, William F. ;
Stappenbeck, Thaddeus S. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (01) :258-269