Role of transcriptional factors Sp1, c-Rel, and c-Jun in LPS-induced C/EBPδ gene expression of mouse macrophages

被引:27
作者
Liu, Y. -W. [1 ]
Chen, C. -C. [1 ]
Wang, J. -M. [2 ,3 ]
Chang, W. -C. [3 ,4 ]
Huang, Y. -C. [1 ]
Chung, S. -Y. [1 ]
Chen, B. -K. [2 ,3 ]
Hung, J. -J. [2 ,3 ]
机构
[1] Natl Chiayi Univ, Coll Life Sci, Grant Inst Biomed & Biopharmaceut Sci, Chiayi 600, Taiwan
[2] Natl Cheng Kung Univ, Inst Biosignal Transduct, Tainan 701, Taiwan
[3] Natl Cheng Kung Univ, Coll Biosci & Biotechnol, Ctr Gene Regulat & Signal Transduct, Tainan 701, Taiwan
[4] Natl Cheng Kung Univ, Coll Med, Dept Pharmacol, Tainan 701, Taiwan
关键词
monocytes/macrophages; transcription factors C/EBP delta; Sp1; c-Rel; c-Jun; NF-kappa B; MAPK; LPS;
D O I
10.1007/s00018-007-7375-5
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
Transcription factor C/EBPs are involved in the regulation of various cellular responses. Here, it was suggested that C/EBP delta gene was activated by lipopolysaccharide (LPS) through transcription factors Sp1, c-Rel, and c-Jun. Assay of the luciferase reporter vectors containing a 5'-deletion of the C/EBP delta gene promoter indicated that a LPS-responsive element was positioned between -345 and -35 bp of mouse C/EBP delta gene promoter. Transcription factors Sp1, c-Rel, and c-Jun bound to this region were identified using both in vivo chromatin immunoprecipitation and in vitro DNA-protein binding assays. LPS enhanced the proteins and DNA binding capacities of c-Rel and c-Jun, and the downstream Sp1 site was essential for LPS-induced C/EBP delta gene. Treatment of cells with ERK/JNK/p38 inhibitors or NF-kappa B inhibitor inhibited the LPS-induced C/EBP delta gene expression by inhibiting c-Jun, c-Rel, and p300 binding to DNA. Our findings provide a better understanding of LPS-induced C/EBP delta gene expression.
引用
收藏
页码:3282 / 3294
页数:13
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