15-Deoxy-Δ12,14-prostaglandin J2-Glycerol Ester, a Putative Metabolite of 2-Arachidonyl Glycerol, Activates Peroxisome Proliferator Activated Receptor γ

被引:32
作者
Raman, Priyadarshini [1 ,2 ]
Kaplan, Barbara L. F. [1 ,2 ]
Thompson, Jerry T. [3 ]
Heuvel, John P. Vanden [3 ]
Kaminski, Norbert E. [1 ,2 ]
机构
[1] Michigan State Univ, Dept Pharmacol & Toxicol, E Lansing, MI 48824 USA
[2] Michigan State Univ, Ctr Integrat Toxicol, E Lansing, MI 48824 USA
[3] Penn State Univ, Dept Vet Sci & Biomed Sci, Ctr Mol Toxicol & Carcinogenesis, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
PPAR-GAMMA; GENE-EXPRESSION; FATTY-ACIDS; CYCLOOXYGENASE-2; EXPRESSION; NUCLEAR RECEPTORS; EPITHELIAL-CELLS; T-CELLS; LIGANDS; IDENTIFICATION; INTERLEUKIN-2;
D O I
10.1124/mol.110.070441
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
2-Arachidonyl glycerol (2-AG) is an endogenous arachidonic acid derivative capable of suppressing interleukin (IL)-2 production by activated T cells. 2-AG-mediated IL-2 suppression is dependent on cyclooxygenase-2 (COX-2) metabolism and peroxisome proliferator activated receptor gamma (PPAR gamma) activation. The objective of the present studies was to examine whether 15-deoxy-Delta(12,14)-PGJ(2)-glycerol ester (15d-PGJ(2)-G), a putative metabolite of 2-AG, can mimic the actions of 2-AG on IL-2 regulation through PPAR gamma activation. 15d-PGJ(2)-G bound PPAR gamma-ligand binding domain in a PPAR gamma competitive binding assay. 15d-PGJ(2)-G treatment activated PPAR gamma in a reporter assay, and PPAR gamma activation was attenuated when a PPAR gamma antagonist, 2-chloro-5-nitro-N-4-pyridinylbenzamide (T0070907), was present. 15d-PGJ(2)-G treatment suppressed IL-2 production by activated Jurkat cells, which was partially attenuated when pretreated with T0070907. Moreover, IL-2 suppression was pronounced when 15d-PGJ(2)-G was present 30 min before or after T-cell activation. Concordant with IL-2 suppression, 15d-PGJ(2)-G treatment decreased nuclear factor of activated T cells (NFAT) transcriptional activity in transiently transfected Jurkat cells. It is noteworthy that T0070907 alone markedly increased NFAT reporter activity, suggesting the existence of endogenous PPAR gamma activation and modulation of NFAT. Because COX-2 metabolism of 2-AG is important for IL-2 suppression, the effect of 2-AG on COX-2 and PPAR gamma mRNA expression was investigated. 2-AG treatment decreased the up-regulation of COX-2 mRNA after T-cell activation, which suggests negative feedback limiting COX-2-mediated metabolism of 2-AG. PPAR gamma mRNA expression was increased upon activation, and 2-AG treatment produced a modest decrease in PPAR gamma mRNA expression. Collectively, our findings suggest that 15d-PGJ(2)-G activates PPAR gamma to decrease NFAT transcriptional activity and IL-2 expression in activated T cells.
引用
收藏
页码:201 / 209
页数:9
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