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15-deoxy-Delta12,14-prostaglandin J2 inhibits glucocorticoid binding and signaling in macrophages through a peroxisome proliferator-activated receptor gamma-independent process.
- Source :
-
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2004 Jun 15; Vol. 172 (12), pp. 7677-83. - Publication Year :
- 2004
-
Abstract
- 15-deoxy-Delta(12,14)-PGJ(2) (15d-PGJ(2)) is involved in the control of inflammatory reaction. We tested the hypothesis that 15d-PGJ(2) would exert this control in part by modulating the sensitivity of inflammatory cells to glucocorticoids. Human U937cells and mouse RAW 264.7 cells were exposed to 15d-PGJ(2), and binding experiments were performed with [(3)H]dexamethasone as a glucocorticoid receptor (GR) ligand. 15d-PGJ(2) caused a transient and concentration-dependent decrease in [(3)H]dexamethasone-specific binding to either cells through a decrease in the number of GR per cell without significant modification of the K(d) value. These changes were related to functional alteration of the GR rather than to a decrease in GR protein. They did not require the engagement of peroxisome proliferator-activated receptor gamma (PPARgamma), because the response to 15d-PGJ(2) was neither mimicked by the PPARgamma agonist ciglitazone nor prevented by the PPARgamma antagonist bisphenol A diglycidyl ether. 15d-PGJ(2) altered GR possibly through the interaction of its cyclopentenone ring with GR cysteine residues because the cyclopentenone ring per se could mimic the effect of 15d-PGJ(2), and modification of GR cysteine residues with methyl methanethiosulfonate suppressed the response to 15d-PGJ(2). Finally, 15d-PGJ(2)-induced decreases in glucocorticoid binding to GR resulted in parallel decreases in the ability of GR to activate the transcription of a glucocorticoid-inducible reporter gene and to reduce the expression of monocyte chemoattractant protein-1. Together these data suggest that 15d-PGJ(2) limits glucocorticoid binding and signaling in monocytes/macrophages through a PPARgamma-independent and cyclopentenone-dependent mechanism. It provides a way in which 15d-PGJ(2) would exert proinflammatory activities in addition to its known anti-inflammatory activities.
- Subjects :
- Animals
Cell Line
Chemokine CCL2 genetics
Cyclopentanes pharmacology
Dexamethasone antagonists & inhibitors
Dexamethasone metabolism
Glucocorticoids metabolism
Humans
Mice
Monocytes metabolism
Prostaglandin D2 analogs & derivatives
Radioligand Assay
Receptors, Glucocorticoid metabolism
Receptors, Glucocorticoid physiology
Transcription, Genetic drug effects
U937 Cells
Glucocorticoids antagonists & inhibitors
Macrophages metabolism
Prostaglandin D2 pharmacology
Receptors, Cytoplasmic and Nuclear
Signal Transduction drug effects
Transcription Factors
Subjects
Details
- Language :
- English
- ISSN :
- 0022-1767
- Volume :
- 172
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of immunology (Baltimore, Md. : 1950)
- Publication Type :
- Academic Journal
- Accession number :
- 15187150
- Full Text :
- https://doi.org/10.4049/jimmunol.172.12.7677