Toll-like receptors as sensors of pathogens

被引:101
作者
Hallman, M
Rämet, M
Ezekowitz, RA
机构
[1] Univ Oulu, Dept Pediat, Oulu 90220, Finland
[2] Univ Oulu, Bioctr Oulu, Oulu 90220, Finland
[3] Massachusetts Gen Hosp Children, Lab Dev Immunol, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02114 USA
关键词
D O I
10.1203/00006450-200109000-00004
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Initial recognition of microbes, as they enter the body, is based on germ line-encoded pattern recognition receptors that selectively bind to essential components of pathogens. This allows the body to respond immediately to the microbial invasion before the development of active immunity. The signal-transducing receptors that trigger the acute inflammatory cascade have been elusive until very recently. On the basis of their genetic similarity to the Toll signaling pathway in Drosophila, mammalian Toll-like receptors (TLRs) have been identified. By now, nine transmembrane proteins in the TLR family have been described. Mammalian TLR4 is the signal-transducing receptor activated by the bacterial lipopolysaccharide. The activation of TLR4 leads to DNA binding of the transcription factor NF-kappaB, resulting in activation of the inflammatory cascade. Activation of other TLRs is likely to have similar consequences. TLR2 mediates the host response to Gram-positive bacteria and yeast. TLR1 and TLR6 may participate in the activation of macrophages by Gram-positive bacteria, whereas TLR9 appears to respond to a specific sequence of bacterial DNA. The TLRs that control the onset of an acute inflammatory response are critical antecedents for the development of adaptive acquired immunity. Genetic and developmental variation in the expression of microbial pattern recognition receptors may affect the individual's predisposition to infections in childhood and may contribute to susceptibility to severe neonatal inflammatory diseases, allergies, and autoimmune diseases.
引用
收藏
页码:315 / 321
页数:7
相关论文
共 59 条
[1]   ESTABLISHMENT OF DORSAL-VENTRAL POLARITY IN THE DROSOPHILA EMBRYO - GENETIC-STUDIES ON THE ROLE OF THE TOLL GENE-PRODUCT [J].
ANDERSON, KV ;
JURGENS, G ;
NUSSLEINVOLHARD, C .
CELL, 1985, 42 (03) :779-789
[2]   TLR4 mutations are associated with endotoxin hyporesponsiveness in humans [J].
Arbour, NC ;
Lorenz, E ;
Schutte, BC ;
Zabner, J ;
Kline, JN ;
Jones, M ;
Frees, K ;
Watt, JL ;
Schwartz, DA .
NATURE GENETICS, 2000, 25 (02) :187-+
[3]   Association of familial deficiency of mannose-binding lectin and meningococcal disease [J].
Bax, WA ;
Cluysenaer, OJJ ;
Bartelink, AKM ;
Aerts, PC ;
Ezekowitz, RAB ;
van Dijk, H .
LANCET, 1999, 354 (9184) :1094-1095
[4]   Tlr4: central component of the sole mammalian LPS sensor [J].
Beutler, B .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (01) :20-26
[5]   Intraamniotic interleukin-1 accelerates surfactant protein synthesis in fetal rabbits and improves lung stability after premature birth [J].
Bry, K ;
Lappalainen, U ;
Hallman, M .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2992-2999
[6]   IMMUNODEFICIENCY DISEASES [J].
BUCKLEY, RH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (20) :2797-2806
[7]   Cloning and characterization of two Toll/interleukin-1 receptor-like genes TIL3 and TIL4: Evidence for a multi-gene receptor family in humans [J].
Chaudhary, PM ;
Ferguson, C ;
Nguyen, V ;
Nguyen, O ;
Massa, HF ;
Eby, M ;
Jasmin, A ;
Trask, BJ ;
Hood, L ;
Nelson, PS .
BLOOD, 1998, 91 (11) :4020-4027
[8]   Collectins and pulmonary host defense [J].
Crouch, EC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 19 (02) :177-201
[9]   A cytokine-responsive I kappa B kinase that activates the transcription factor NF-kappa B [J].
DiDonato, JA ;
Hayakawa, M ;
Rothwarf, DM ;
Zandi, E ;
Karin, M .
NATURE, 1997, 388 (6642) :548-554
[10]   Analysis of Tlr4-mediated LPS signal transduction in macrophages by mutational modification of the receptor [J].
Du, X ;
Poltorak, A ;
Silva, M ;
Beutler, B .
BLOOD CELLS MOLECULES AND DISEASES, 1999, 25 (21) :328-338