Combinatorial roles of nuclear receptors in inflammation and immunity

被引:360
作者
Glass, CK
Ogawa, S
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Tokyo, Dept Geriatr Med, Bunkyo Ku, Tokyo 1138655, Japan
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nri1748
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Members of the nuclear-receptor superfamily have well-documented regulatory effects on inflammatory processes. Recent work has highlighted the roles of peroxisome-proliferator-activated receptors (PPARs) and liver X receptors (LXRs) in controlling metabolic and inflammatory programmes of gene expression in macrophages and lymphocytes. Here, we describe recent studies that extend our understanding of how these nuclear receptors, through their interactions with transcription factors and other cell-signalling systems, have important regulatory roles in innate and adaptive immunity. We suggest that by using receptor-specific mechanisms, PPARs and LXRs function in a combinatorial manner with the glucocorticoid receptor to integrate local and systemic responses to inflammation.
引用
收藏
页码:44 / 55
页数:12
相关论文
共 132 条
[1]  
Adcock Ian M., 1996, Biochemical Society Transactions, V24, p267S
[2]   Regulation of cytokine and cytokine receptor expression by glucocorticoids [J].
Almawi, WY ;
Beyhum, HN ;
Rahme, AA ;
Rieder, MJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 60 (05) :563-572
[3]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[4]   A nuclear receptor atlas: Macrophage activation [J].
Barish, GD ;
Downes, M ;
Alaynick, WA ;
Yu, RT ;
Ocampo, CB ;
Bookout, AL ;
Mangelsdorf, DJ ;
Evans, RM .
MOLECULAR ENDOCRINOLOGY, 2005, 19 (10) :2466-2477
[5]   CRYSTAL-STRUCTURE OF THE LIGAND-BINDING DOMAIN OF THE HUMAN NUCLEAR RECEPTOR RXR-ALPHA [J].
BOURGUET, W ;
RUFF, M ;
CHAMBON, P ;
GRONEMEYER, H ;
MORAS, D .
NATURE, 1995, 375 (6530) :377-382
[6]   Molecular basis of agonism and antagonism in the oestrogen receptor [J].
Brzozowski, AM ;
Pike, ACW ;
Dauter, Z ;
Hubbard, RE ;
Bonn, T ;
Engstrom, O ;
Ohman, L ;
Greene, GL ;
Gustafsson, JA ;
Carlquist, M .
NATURE, 1997, 389 (6652) :753-758
[7]   Nuclear hormone receptor antagonism with AP-1 by inhibition of the JNK pathway [J].
Caelles, C ;
González-Sancho, JM ;
Muñoz, A .
GENES & DEVELOPMENT, 1997, 11 (24) :3351-3364
[8]   PPARs in atherosclerosis: the clot thickens [J].
Castrillo, A ;
Tontonoz, P .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (11) :1538-1540
[9]   Liver X receptor-dependent repression of matrix metalloproteinase-9 expression in macrophages [J].
Castrillo, A ;
Joseph, SB ;
Marathe, C ;
Mangelsdorf, DJ ;
Tontonoz, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (12) :10443-10449
[10]   Crosstalk between LXR and Toll-like receptor signaling mediates bacterial and viral antagonism of cholesterol metabolism [J].
Castrillo, A ;
Joseph, SB ;
Vaidya, SA ;
Haberland, M ;
Fogelman, AM ;
Cheng, GH ;
Tontonoz, P .
MOLECULAR CELL, 2003, 12 (04) :805-816