Nucleosome remodeling at the IL-12 p40 promoter is a TLR-dependent, Rel-independent event

被引:142
作者
Weinmann, AS
Mitchell, DM
Sanjabi, S
Bradley, MN
Hoffmann, A
Liou, HC
Smale, ST [1 ]
机构
[1] Univ Calif Los Angeles, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
[3] CALTECH, Dept Biol, Pasadena, CA 91125 USA
[4] Cornell Univ, Coll Med, Dept Med, Div Immunol, New York, NY 10021 USA
关键词
D O I
10.1038/83168
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lipopolysaccharide (LPS) induction of the gene encoding interleukin 12 p40 requires remodeling of a promoter-encompassing nucleosome and the Toll-like receptor (TLR)-mediated activation of a c-Re1-containing complex. Analysis of TLR4-mutant mice revealed that remodeling requires TLR signaling. However, Re1 proteins and other proteins required for transcription of an integrated p40 promoter were insufficient for remodeling. c-Re1 was also unnecessary for remodeling, as remodeling was observed in c-Re1(-/-) macrophages, which lack p40 transcripts. These results suggest that remodeling requires TLR signaling pathways that diverge from the c-Re1 activation pathways. The factors that stimulate remodeling may represent, therefore, newly identified targets of TLR signaling and of agents that regulate inflammatory responses and T(H)1 development.
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收藏
页码:51 / 57
页数:7
相关论文
共 31 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   Cell activation and apoptosis by bacterial lipoproteins through toll-like receptor-2 [J].
Aliprantis, AO ;
Yang, RB ;
Mark, MR ;
Suggett, S ;
Devaux, B ;
Radolf, JD ;
Klimpel, GR ;
Godowski, P ;
Zychlinsky, A .
SCIENCE, 1999, 285 (5428) :736-739
[3]   Tlr4: central component of the sole mammalian LPS sensor [J].
Beutler, B .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (01) :20-26
[4]   Host defense mechanisms triggered by microbial lipoproteins through toll-like receptors [J].
Brightbill, HD ;
Libraty, DH ;
Krutzik, SR ;
Yang, RB ;
Belisle, JT ;
Bleharski, JR ;
Maitland, M ;
Norgard, MV ;
Plevy, SE ;
Smale, ST ;
Brennan, PJ ;
Bloom, BR ;
Godowski, PJ ;
Modlin, RL .
SCIENCE, 1999, 285 (5428) :732-736
[5]  
De Maeyer Edward, 1998, P491
[6]  
GORDON S, 1999, FUNDAMENTAL IMMUNOLO, P533
[7]   Activation of the transcription factor MEF2C by the MAP kinase p38 in inflammation [J].
Han, J ;
Jiang, Y ;
Li, Z ;
Kravchenko, VV ;
Ulevitch, RJ .
NATURE, 1997, 386 (6622) :296-299
[8]   Dissecting the regulatory circuitry of a eukaryotic genome [J].
Holstege, FCP ;
Jennings, EG ;
Wyrick, JJ ;
Lee, TI ;
Hengartner, CJ ;
Green, MR ;
Golub, TR ;
Lander, ES ;
Young, RA .
CELL, 1998, 95 (05) :717-728
[9]   Unresponsiveness of MyD88-deficient mice to endotoxin [J].
Kawai, T ;
Adachi, O ;
Ogawa, T ;
Takeda, K ;
Akira, S .
IMMUNITY, 1999, 11 (01) :115-122
[10]   A C/EBPβ isoform recruits the SWI/SNF complex to activate myeloid genes [J].
Kowenz-Leutz, E ;
Leutz, A .
MOLECULAR CELL, 1999, 4 (05) :735-743