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

被引:141
|
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.
引用
收藏
页码:51 / 57
页数:7
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