NF-κB elements contribute to junB inducibility by lipopolysaccharide in the murine macrophage cell line RAW264.7

被引:23
作者
Frazier-Jessen, MR
Thompson, CD
Brown, R
Rawat, R
Nordan, RP
Feldman, GM
机构
[1] US FDA, Immunobiol Lab,Ctr Biol Evaluat & Res, Div Monoclonal Antibodies, Off Therapeut Res & Review, Bethesda, MD 20892 USA
[2] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
关键词
lipopolysaccharide; junB; macrophage; nuclear factor kappa B;
D O I
10.1016/S0014-5793(02)02295-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages respond to bacterial lipopolysaccharide (LPS) by activating latent cis-acting factors that initiate transcription of immediate early genes. One such immediate early gene, junB, is induced by LPS in macrophages within 30 min. To identify elements that mediate the induction of junB by LPS, upstream and downstream sequences flanking the junB gene were examined by transient expression in the RAW264.7 murine macrophage cell line using a luciferase reporter gene vector containing the junB minimal promoter. A > 10-fold enhancement was associated with a 222 bp region downstream of the junB promoter in response to LPS. Transient reporter assays demonstrated that multiple nuclear factor (NIT) kappaB sites are required for inducibility of junB by LPS in RAW264.7 cells. Electrophoretic mobility shift assays confirmed binding of LPS-induced nuclear proteins included p50/p65 heterodimers at these NF-kappaB sites. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:203 / 207
页数:5
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