期刊
IMMUNOLOGY LETTERS
卷 191, 期 -, 页码 63-72出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.imlet.2017.09.009
关键词
Prostaglandin E-2; Regulatory T cells; Foxp3; Protein kinase A
类别
资金
- Nature Science Foundation of Hebei Province [H2015206378]
- Education Department of HeBei Province Top Notch Talent Project Fund [BJ2014045]
- Colleges and Universities in HeBei Province Scientific Research Project High Level Talents Fund [GCC2014004]
- National Science Foundation of China [81601876]
Regulatory T cells (Treg cells) belong to a class of immunosuppressive cells that control the pathological changes of autoimmunity and inflammation. Prostaglandin E-2 (PGE(2)) is a potent lipid mediator of immune inflammation including rheumatoid arthritis (RA) that exerts its effects via four subtypes of G-protein-coupled receptors (EP1-4). The ability of PGE(2) to regulate human Treg differentiation has not yet been reported. In the current study, we investigated the effects of PGE(2) on the differentiation of naive T cells from healthy and RA patients into Treg cells and the intracellular signaling involved in this process in vitro. Our data indicate that PGE(2) negatively influenced the percentage of Treg cells and Foxp3 mRNA expression. The regulatory effects of PGE(2) were associated with increased intracellular cAMP levels and PKA activity. EP2 receptors may mediate the inhibitory role of PGE(2), since PGE(2) actions were mimicked by EP2 agonist (Butaprost) and cAMP agonist (Sp-8-CPT-cAMPS) but were reversed by an EP2 antagonist (PF-04418948) and a PICA inhibitor (H-89). PGE(2) negatively modulated the expression of cytotoxic T lymphocyte antigen-4 (CTLA-4) and glucocorticoid-induced tumor necrosis factor receptor-related protein (GITR), as well as the production of interleukin (IL)-10 by Treg cells via EP2 receptors and cAMP/PKA signaling. All these findings indicate that PGE(2) can inhibit Treg differentiation mediated through the EP2-cAMP/PKA signaling pathway, and suggest novel immune-based therapies for use in RA treatment.
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