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Inhibition of IL-10-induced STAT3 activation by 15-deoxy-Δ12,14-prostaglandin J<inf>2</inf>

Authors :
Ji, J. D.
Kim, H. J.
Rho, Y. H.
Choi, S. J.
Lee, Y. H.
Cheon, H. J.
Sohn, J.
Song, G. G.
Source :
Rheumatology; August 2005, Vol. 44 Issue: 8 p983-988, 6p
Publication Year :
2005

Abstract

Objectives. 15-Deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2) is a natural ligand that activates the peroxisome proliferator-activated receptor (PPAR)-γ, a member of the nuclear receptor family implicated in the regulation of lipid metabolism and adipocyte differentiation. Recent data have shown that 15d-PGJ2 exerts anti-inflammatory action via inhibition of the interferon γ (IFN-γ)-induced Jak-STAT signalling pathway. The anti-inflammatory effect of IL-10 is mediated via activated STAT3 (signal transducer and activator of transcription 3). In this study, we investigated whether 15d-PGJ2 inhibit IL-10-induced STAT activation.Methods. We used western blotting, flow cytometric analysis and a real-time polymerase chain reaction.Results. 15d-PGJ2 blocked IL-10-induced STAT1 and STAT3 activation in primary human monocytes, macrophages and THP-1 cells. Inhibition was not specific for IL-10, as induction of STAT activation by IFN-γ and IL-6 was also inhibited by 15d-PGJ2. Inhibition of IL-10 signalling was induced within 1 h after pretreatment of 15d-PGJ2. Other PPARγ agonists, such as troglitazone, did not inhibit IL-10 signalling. Treatment with GW9662, a specific PPARγ antagonist, had no effect on 15d-PGJ2-mediated inhibition of IL-10 signalling even at higher concentrations (50 μM), indicating that 15d-PGJ2 affects the IL-10-induced Jak-STAT signalling pathway via an PPARγ-independent mechanism. Actinomycin D had no effect on 15d-PGJ2-mediated inhibition of IL-10 signalling, indicating that inhibition of IL-10 signalling occurs independently of de novo gene expression. Also, inhibitors of extracellular signal-regulated kinase (ERKs) (PD98059), p38 MAPK (mitogen-activated protein kinase) (SB203580) and protein kinase C (PKC) (GF109203X, calphostin C) had no effect on 15d-PGJ2-mediated inhibition of IL-10 signalling. These results show that MAPKs and PKC are not involved in the inhibition of IL-10 signalling.Conclusions. We showed that 15d-PGJ2 non-specifically inhibits STAT signalling of the anti-inflammatory cytokine IL-10 as well as the proinflammatory cytokine IFN-γ. These findings indicate the possibility that 15d-PGJ2 can have adverse effects in the management of diseases in which IL-10 plays a critical role in the suppression of inflammation.

Details

Language :
English
ISSN :
14620324 and 14620332
Volume :
44
Issue :
8
Database :
Supplemental Index
Journal :
Rheumatology
Publication Type :
Periodical
Accession number :
ejs7470002
Full Text :
https://doi.org/10.1093/rheumatology/keh657