Front Immunol. 2013 Jun 04;4:130. doi: 10.3389/fimmu.2013.00130. eCollection 2013.
Proinflammatory and immunoregulatory roles of eicosanoids in T cells.
Frontiers in immunology
Anna Mari Lone, Kjetil Taskén
Affiliations
Affiliations
- Centre for Molecular Medicine Norway, Nordic EMBL Partnership, University of Oslo and Oslo University Hospital , Oslo , Norway ; Biotechnology Centre, University of Oslo , Oslo , Norway ; K.G. Jebsen Inflammation Research Centre, University of Oslo , Oslo , Norway.
PMID: 23760108
PMCID: PMC3671288 DOI: 10.3389/fimmu.2013.00130
Abstract
Eicosanoids are inflammatory mediators primarily generated by hydrolysis of membrane phospholipids by phospholipase A2 to ω-3 and ω-6 C20 fatty acids that next are converted to leukotrienes (LTs), prostaglandins (PGs), prostacyclins (PCs), and thromboxanes (TXAs). The rate-limiting and tightly regulated lipoxygenases control synthesis of LTs while the equally well-controlled cyclooxygenases 1 and 2 generate prostanoids, including PGs, PCs, and TXAs. While many of the classical signs of inflammation such as redness, swelling, pain, and heat are caused by eicosanoid species with vasoactive, pyretic, and pain-inducing effects locally, some eicosanoids also regulate T cell functions. Here, we will review eicosanoid production in T cell subsets and the inflammatory and immunoregulatory functions of LTs, PGs, PCs, and TXAs in T cells.
Keywords: cAMP; cyclooxygenase 2; immunoregulation effect; inflammation; inflammation mediators; leukotrienes; prostaglandins; regulatory T cells
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