Polyunsaturated fatty acid-derived lipid mediators and T cell function

被引:52
作者
Nicolaou, Anna [1 ]
Mauro, Claudio [2 ]
Urquhart, Paula [1 ]
Marelli-Berg, Federica [2 ]
机构
[1] Univ Manchester, Fac Med & Human Sci, Manchester Pharm Sch, Manchester M13 9PT, Lancs, England
[2] Queen Mary Univ London, William Harvey Res Inst, Ctr Biochem Pharmacol, London, England
基金
英国惠康基金;
关键词
T cells; polyunsaturated fatty acids; eicosanoids; prostaglandins; leukotrienes; cyclooxygenase; lipoxygenase; endocannabinoids; LEUKOTRIENE B-4 RECEPTOR; GAMMA-LINOLENIC ACID; HELPER TYPE-2 CELLS; DIETARY FISH-OIL; DENDRITIC CELLS; PROSTAGLANDIN D-2; CYTOKINE PRODUCTION; TH2; CELLS; EICOSAPENTAENOIC ACID; ARACHIDONIC-ACID;
D O I
10.3389/fimmu.2014.00075
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fatty acids are involved in T cell biology both as nutrients important for energy production as well as signaling molecules. In particular, polyunsaturated fatty acids are known to exhibit a range of immunomodulatory properties that progress through T cell mediated events, although the molecular mechanisms of these actions have not yet been fully elucidated. Some of these immune activities are linked to polyunsaturated fatty acid-induced alteration of the composition of cellular membranes and the consequent changes in signaling pathways linked to membrane raft-associated proteins. However, significant aspects of the polyunsaturated fatty acid bioactivities are mediated through their transformation to specific lipid mediators, products of cyclooxygenase, lipoxygenase, or cytochrome P450 enzymatic reactions. Resulting bioactive metabolites including prostaglandins, leukotrienes, and endocannabinoids are produced by and/or act upon T leukocytes through cell surface receptors and have been shown to alter T cell activation and differentiation, proliferation, cytokine production, motility, and homing events. Detailed appreciation of the mode of action of these lipids presents opportunities for the design and development of therapeutic strategies aimed at regulating T cell function.
引用
收藏
页码:1 / 15
页数:15
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