Critical role of toll-like receptors and nucleotide oligomerisation domain in the regulation of health and disease

被引:108
作者
Mitchell, Jane A. [1 ]
Paul-Clark, Mark J. [1 ]
Clarke, Graham W. [1 ]
McMaster, Shaun K. [1 ]
Cartwright, Neil [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Royal Brompton Hosp, Natl Heart & Lung Inst, Unit Crit Care Med, London SW3 6LY, England
关键词
D O I
10.1677/JOE-07-0067
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pathogens are sensed by pattern recognition receptors (PRRs), which are germ line-encoded receptors, including transmembrane Toll-like receptors (TLRs) and cytosolic nucleotide oligomerisation domain (NOD) proteins, containing leucine-rich repeats (NLRs). Activation of PRRs by specific pathogen-associated molecular patterns (PAMPs) results in genomic responses in host cells involving activation transcription factors and the induction of genes. There are now at least 10 TLRs in humans and 13 in mice, and 2 NLRs (NOD1 and NOD2). TLR signalling is via interactions with adaptor proteins including MyD88 and toll-receptor associated activator of interferon (TRIF). NOD signalling is via the inflarnmasome and involves activation of Rip-like interactive clarp kinase (RICK). Bacterial lipopolysaccharide (LPS) from Gram-negative bacteria is the best-studied PAMP and is activated by or 'sensed' by TLR4. Lipoteichoic acid (LTA) from Gram-positive bacteria is sensed by TLR2. TLR4 and TLR2 have different signalling cascades, although activation of either results in symptoms of sepsis and shock. This review describes the rapidly expanding field of pathogen-sensing receptors and uses LPS and LTA as examples ofhow these pathways parallel and diverge from each other. The role of pathogen-sensing pathways in disease is also discussed.
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页码:323 / 330
页数:8
相关论文
共 75 条
[1]   TLR signaling in the gut in health and disease [J].
Abreu, MT ;
Fukata, M ;
Arditi, M .
JOURNAL OF IMMUNOLOGY, 2005, 174 (08) :4453-4460
[2]  
Ajuebor MN, 1999, J IMMUNOL, V162, P1685
[3]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[4]   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
[5]   ESTABLISHMENT OF DORSAL-VENTRAL POLARITY IN THE DROSOPHILA EMBRYO - THE INDUCTION OF POLARITY BY THE TOLL GENE-PRODUCT [J].
ANDERSON, KV ;
BOKLA, L ;
NUSSLEINVOLHARD, C .
CELL, 1985, 42 (03) :791-798
[6]   A conserved signaling pathway: The Drosophila Toll-Dorsal pathway [J].
Belvin, MP ;
Anderson, KV .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1996, 12 :393-416
[7]   Characterization of the induction of nitric oxide synthase and cyclo-oxygenase in rat aorta in organ culture [J].
BishopBailey, D ;
Larkin, SW ;
Warner, TD ;
Chen, G ;
Mitchell, JA .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (01) :125-133
[8]   Reduced atherosclerosis in MyD88-null mice links elevated serum cholesterol levels to activation of innate immunity signaling pathways [J].
Björkbacka, H ;
Kunjathoor, VV ;
Moore, KJ ;
Koehn, S ;
Ordija, CM ;
Lee, MA ;
Means, T ;
Halmen, K ;
Luster, AD ;
Golenbock, DT ;
Freeman, MW .
NATURE MEDICINE, 2004, 10 (04) :416-421
[9]   The role of toll-like receptors in the immune-adrenal crosstalk [J].
Bornstein, S. R. ;
Ziegler, C. G. ;
Krug, A. W. ;
Kanczkowski, W. ;
Rettori, V. ;
McCann, S. M. ;
Wirth, M. ;
Zacharowski, K. .
NEUROENDOCRINE AND IMMUNE CROSSTALK, 2006, 1088 :307-318
[10]   Impaired adrenal stress response in Toll-like receptor 2-deficient mice [J].
Bornstein, SR ;
Zacharowski, P ;
Schumann, RR ;
Barthel, A ;
Tran, N ;
Papewalis, C ;
Rettori, V ;
McCann, SM ;
Schulze-Osthoff, K ;
Scherbaum, WA ;
Tarnow, J ;
Zacharowski, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (47) :16695-16700