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Bacterial peptidoglycan induces CD14-dependent activation of transcription factors CREB/ATF and AP-1.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 1999 May 14; Vol. 274 (20), pp. 14012-20. - Publication Year :
- 1999
-
Abstract
- Peptidoglycan (PGN), the major cell wall component of Gram-positive bacteria, induces secretion of cytokines in macrophages through CD14, the pattern recognition receptor that binds lipopolysaccharide and other microbial products. To begin to elucidate the mechanisms that regulate the transcription of cytokine genes, we wanted to determine which transcription factors are activated by PGN in mouse RAW264.7 and human THP-1 macrophage cells. Our results demonstrated that: (i) PGN induced phosphorylation of the transcription factors ATF-1 and CREB; (ii) ATF-1 and CREB bound DNA as a dimer and induced transcriptional activation of a CRE reporter plasmid, which was inhibited by dominant negative CREB and ATF-1; (iii) PGN induced phosphorylation of c-Jun, protein synthesis of JunB and c-Fos, and transcriptional activation of the AP-1 reporter plasmid, which was inhibited by dominant negative c-Fos; and (iv) PGN-induced activation of CREB/ATF and AP-1 was mediated through CD14. This is the first study to demonstrate activation of CREB/ATF and AP-1 transcription factors by PGN or by any other component of Gram-positive bacteria.
- Subjects :
- Activating Transcription Factor 1
Animals
Cell Line
Consensus Sequence
Cyclic AMP Response Element-Binding Protein
Humans
Lipopolysaccharides pharmacology
Lysostaphin pharmacology
Macrophages drug effects
Macrophages metabolism
Mice
Monocytes drug effects
Monocytes metabolism
Muramidase metabolism
Phosphorylation
Proto-Oncogene Proteins c-fos metabolism
Proto-Oncogene Proteins c-jun metabolism
Salmonella
Transcription Factors metabolism
DNA-Binding Proteins
Lipopolysaccharide Receptors metabolism
Peptidoglycan metabolism
Transcription Factor AP-1 metabolism
Transcriptional Activation
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 274
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 10318814
- Full Text :
- https://doi.org/10.1074/jbc.274.20.14012