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C646 modulates inflammatory response and antibacterial activity of macrophage.
- Source :
-
International immunopharmacology [Int Immunopharmacol] 2019 Sep; Vol. 74, pp. 105736. Date of Electronic Publication: 2019 Jul 11. - Publication Year :
- 2019
-
Abstract
- C646 is a newly discovered competitive p300/CREB-binding protein-specific inhibitor. Previous studies have shown its potential antitumor activity, but the immunomodulatory function of C646 remains largely unknown. In this study, we investigated the effects of C646 in cytokine expression and antibacterial activity in mouse macrophages. Results showed that C646 significantly reduced LPS-induced pro-inflammatory cytokines, which relied on suppression of JNK, ERK1/2, and NF-κB p65 signaling pathways. In addition, the inhibitory effects were not associated with modulating the expression of CD14/TLR4/MD2 complex or antagonizing its binding ability to LPS. Furthermore, C646 also down-regulated the levels of FcγR III/II and CR3 on macrophage, impaired the phagocytic ability against E. coli, and blocked phagosome-lysosome fusion. Consistent with this, C646 inhibited macrophage-associated bactericidal ability. Collectively, these data indicated that C646 exhibited potent immunomodulatory effects on macrophage both in the production of pro-inflammatory cytokines and bacterial phagocytosis.<br /> (Copyright © 2019 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Antigens, Bacterial immunology
Cells, Cultured
Complement C3 metabolism
Immunomodulation
Lipopolysaccharides immunology
Macrophages immunology
Male
Mice
Mice, Inbred C57BL
NF-kappa B metabolism
Nitrobenzenes
Phagocytosis drug effects
Pyrazolones
Signal Transduction
Benzoates pharmacology
Escherichia coli physiology
Escherichia coli Infections drug therapy
Inflammation drug therapy
Macrophages drug effects
Pyrazoles pharmacology
p300-CBP Transcription Factors antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1705
- Volume :
- 74
- Database :
- MEDLINE
- Journal :
- International immunopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 31302452
- Full Text :
- https://doi.org/10.1016/j.intimp.2019.105736