Lipid Mediators in Inflammation

被引:143
作者
Bennett, Melanie [1 ]
Gilroy, Derek W. [2 ]
机构
[1] Roche Prod Ltd, Shire Pk, Welwyn Garden City AL7 1TW, Herts, England
[2] UCL, Ctr Clin Pharmacol & Therapeut, Div Med, London WC1 E6JJ, England
关键词
NF-KAPPA-B; ASPIRIN-TRIGGERED LIPOXIN; ACTIVATED RECEPTOR-GAMMA; IL-8; GENE-EXPRESSION; INCREASED VASCULAR-PERMEABILITY; PROSTAGLANDIN-LIKE ACTIVITY; SOLUBLE EPOXIDE HYDROLASE; COLONY-STIMULATING FACTOR; PROTEIN-COUPLED RECEPTOR; PULMONARY HOST-DEFENSE;
D O I
10.1128/microbiolspec.MCHD-0035-2016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lipids are potent signaling molecules that regulate a multitude of cellular responses, including cell growth and death and inflammation/infection, via receptor-mediated pathways. Derived from polyunsaturated fatty acids (PUFAs), such as arachidonic acid (AA), eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA), each lipid displays unique properties, thus making their role in inflammation distinct from that of other lipids derived from the same PUFA. This diversity arises from their synthesis, which occurs via discrete enzymatic pathways and because they elicit responses via different receptors. This review will collate the bioactive lipid research to date and summarize the major pathways involved in their biosynthesis and role in inflammation. Specifically, lipids derived from AA (prostanoids, leukotrienes, 5-oxo-6,8,11,14-eicosatetraenoic acid, lipoxins, and epoxyeicosatrienoic acids), EPA (E-series resolvins), and DHA (D-series resolvins, protectins, and maresins) will be discussed herein.
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页数:21
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