Expression and regulation of interleukin-1 receptors in the brain.: Role in cytokines-induced sickness behavior

被引:115
作者
Parnet, P
Kelley, KW
Bluthé, RM
Dantzer, R
机构
[1] Inst Francois Magendie, INRA, Lab Integrat Neurobiol, INSERM,U394, F-33077 Bordeaux, France
[2] Univ Illinois, Dept Anim Sci, Immunophysiol Lab, Edward R Madigan Lab 207, Urbana, IL 61801 USA
关键词
interleukin-1; receptor; brain; sickness behavior;
D O I
10.1016/S0165-5728(02)00022-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sickness behavior refers to the coordinated set of behavior changes that develop in sick individuals during the course of an infection. At the molecular level, these changes are due to the effects of proinflammatory cytokines as interleukin-1 on the brain. The purpose of this article is not to review the entire field of cytokines and behavior, but rather to address the role of interleukin-1 receptors (IL-1Rs,) in sickness behavior. We briefly describe the notion of sickness behavior and present the distribution of IL-1Rs in the central nervous system of the human, mouse and rat. We then bring arguments in favor of the functionality of the various subtypes of receptors and evaluate the nature of the signaling pathways activated by brain IL-1Rs to initiate central modifications leading to symptoms of sickness. Finally, modulation of IL-1 action on its receptor by various opposing factors including glucocorticoids and anti-inflammatory cytokines is discussed. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:5 / 14
页数:10
相关论文
共 75 条
[31]   MOLECULAR-CLONING AND CHARACTERIZATION OF A 2ND SUBUNIT OF THE INTERLEUKIN-1 RECEPTOR COMPLEX [J].
GREENFEDER, SA ;
NUNES, P ;
KWEE, L ;
LABOW, M ;
CHIZZONITE, PA ;
JU, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (23) :13757-13765
[32]   BIOLOGICAL BASIS OF THE BEHAVIOR OF SICK ANIMALS [J].
HART, BL .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1988, 12 (02) :123-137
[33]  
Herkenham M, 1998, J COMP NEUROL, V400, P175, DOI 10.1002/(SICI)1096-9861(19981019)400:2<175::AID-CNE2>3.0.CO
[34]  
2-6
[35]   Interleukin-1β system (ligand, receptor type I, receptor accessory protein and receptor antagonist), TNF-α, TGF-β1 and neuropeptide Y mRNAs in specific brain regions during bacterial LPS-induced anorexia [J].
Ilyin, SE ;
Gayle, D ;
Flynn, MC ;
Plata-Salamán, CR .
BRAIN RESEARCH BULLETIN, 1998, 45 (05) :507-515
[36]   Temporal and spatial relationships between lipopolysaccharide-induced expression of fos, interleukin-1β and inducible nitric oxide synthase in rat brain [J].
Konsman, JP ;
Kelley, K ;
Dantzer, R .
NEUROSCIENCE, 1999, 89 (02) :535-548
[37]   Nuclear factor-κB inhibitor peptide inhibits spontaneous and interleukin-1β-induced sleep [J].
Kubota, T ;
Kushikata, T ;
Fang, JD ;
Krueger, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 279 (02) :R404-R413
[38]   An essential role of interleukin-1β in mediating NF-κB activity and COX-2 transcription in cells of the blood-brain barrier in response to a systemic and localized inflammation but not during endotoxemia [J].
Laflamme, N ;
Lacroix, S ;
Rivest, S .
JOURNAL OF NEUROSCIENCE, 1999, 19 (24) :10923-10930
[39]   Toll-like receptor 4: the missing link of the cerebral innate immune response triggered by circulating gram-negative bacterial cell wall components [J].
Laflamme, N ;
Rivest, S .
FASEB JOURNAL, 2001, 15 (01) :155-163
[40]  
Lang D, 1998, J IMMUNOL, V161, P6871