Source:http://linkedlifedata.com/resource/pubmed/id/17273900
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0017337,
umls-concept:C0024432,
umls-concept:C0025914,
umls-concept:C0026809,
umls-concept:C0030958,
umls-concept:C0033684,
umls-concept:C0040649,
umls-concept:C0185117,
umls-concept:C0439097,
umls-concept:C1547348,
umls-concept:C1705241,
umls-concept:C2349975,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
2007-6-1
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pubmed:abstractText |
Peptidoglycan-activated gene expression is mediated through various transcription factors including CCAAT/enhancer-binding protein delta (C/EBPdelta). The purpose of the present study is to elucidate the mechanism of PGN-activated C/EBPdelta gene. PGN stimulated C/EBPdelta protein and mRNA expression in mouse macrophages RAW 264.7 cells. Analysis of C/EBPdelta promoter activity by luciferase reporter assay indicated that PGN-induced C/EBPdelta gene activation is partially mediated by the -345 to +24 bp of C/EBPdelta gene promoter. The in vitro protein-DNA binding assay showed that Sp1, c-Rel and c-Jun are the major protein binding to this PGN-response element of C/EBPdelta promoter, and the binding of c-Rel and c-Jun is increased after PGN treatment. All of these binding activities were abolished when Sp1-, NF-kappaB/APRE-, CRE-sites were mutated. Furthermore, analysis of this promoter region by site-directed mutants constructed in luciferase reporter vector indicated that two Sp1-sites, one NF-kappaB/APRE-site and one CRE-site are prominent for PGN-induced gene expression. In addition, when Sp1, c-Rel or c-Jun transcription factors were overexpressed in cells, all of them enhanced C/EBPdelta promoter activity. In summary, we suggest that Sp1, c-Rel and c-Jun transcription factors play important roles in activation of C/EBPdelta gene promoter under the stimulation of PGN. Given the importance of C/EBPdelta in inflammatory disease, these results reveal a clue as a potential therapeutic target for suppression of C/EBPdelta expression under PGN stimulation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCAAT-Enhancer-Binding Protein-delta,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptidoglycan,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1021-7770
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
407-18
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17273900-Animals,
pubmed-meshheading:17273900-CCAAT-Enhancer-Binding Protein-delta,
pubmed-meshheading:17273900-DNA-Binding Proteins,
pubmed-meshheading:17273900-Gene Expression Regulation,
pubmed-meshheading:17273900-Macrophages,
pubmed-meshheading:17273900-Mice,
pubmed-meshheading:17273900-Peptidoglycan,
pubmed-meshheading:17273900-Promoter Regions, Genetic,
pubmed-meshheading:17273900-Transcription, Genetic,
pubmed-meshheading:17273900-Transcription Factors,
pubmed-meshheading:17273900-Transcriptional Activation,
pubmed-meshheading:17273900-Up-Regulation
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pubmed:year |
2007
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pubmed:articleTitle |
Peptidoglycan enhances transcriptional expression of CCAAT/enhancer-binding protein delta gene in mouse macrophages.
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pubmed:affiliation |
Graduate Institute of Biopharmaceutics, College of Life Sciences, National Chiayi University, Chiayi, 600, Taiwan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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