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Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells
Eicosanoids are inflammatory mediators primarily generated by hydrolysis of membrane phospholipids by phospholipase A2 to ω-3 and ω-6 C(20) fatty acids that next are converted to leukotrienes (LTs), prostaglandins (PGs), prostacyclins (PCs), and thromboxanes (TXAs). The rate-limiting and tightly reg...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671288/ https://www.ncbi.nlm.nih.gov/pubmed/23760108 http://dx.doi.org/10.3389/fimmu.2013.00130 |
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author | Lone, Anna Mari Taskén, Kjetil |
author_facet | Lone, Anna Mari Taskén, Kjetil |
author_sort | Lone, Anna Mari |
collection | PubMed |
description | Eicosanoids are inflammatory mediators primarily generated by hydrolysis of membrane phospholipids by phospholipase A2 to ω-3 and ω-6 C(20) 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. |
format | Online Article Text |
id | pubmed-3671288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36712882013-06-11 Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells Lone, Anna Mari Taskén, Kjetil Front Immunol Immunology Eicosanoids are inflammatory mediators primarily generated by hydrolysis of membrane phospholipids by phospholipase A2 to ω-3 and ω-6 C(20) 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. Frontiers Media S.A. 2013-06-04 /pmc/articles/PMC3671288/ /pubmed/23760108 http://dx.doi.org/10.3389/fimmu.2013.00130 Text en Copyright © 2013 Lone and Taskén. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Immunology Lone, Anna Mari Taskén, Kjetil Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells |
title | Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells |
title_full | Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells |
title_fullStr | Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells |
title_full_unstemmed | Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells |
title_short | Proinflammatory and Immunoregulatory Roles of Eicosanoids in T Cells |
title_sort | proinflammatory and immunoregulatory roles of eicosanoids in t cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671288/ https://www.ncbi.nlm.nih.gov/pubmed/23760108 http://dx.doi.org/10.3389/fimmu.2013.00130 |
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