Mediator lipidomics in acute inflammation and resolution

被引:107
作者
Arita, Makoto [1 ,2 ]
机构
[1] Univ Tokyo, Dept Hlth Chem, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
eosinophil; lipid mediator; metabolomics; n-3; PUFA; resolution of inflammation; PRO-RESOLVING MEDIATORS; ANTIINFLAMMATORY ACTIONS; RECEPTORS; OMEGA-3-FATTY-ACIDS; IDENTIFICATION; BIOSYNTHESIS; LEUKOTRIENES; PROTECTIN-D1; ASSIGNMENTS; METABOLISM;
D O I
10.1093/jb/mvs092
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Acute inflammation is an indispensable host response to foreign challenges or tissue injury. In healthy conditions, inflammatory processes are self-limiting and self-resolving, suggesting the existence of endogenous mechanisms for the control of inflammation and resolution. A comprehensive understanding of the cellular and molecular events of a well-orchestrated inflammatory response is required, and recent studies have uncovered the roles of endogenous lipid mediators derived from polyunsaturated fatty acids (i.e. lipoxins, resolvins, protectins) in controlling the resolution of inflammation. This review presents recent advances in understanding the formation and action of these mediators, especially focusing on the LC-MS/MS-based lipidomics approach and the emerging roles of eosinophils and eosinophil-derived lipid mediators in controlling acute inflammation and resolution.
引用
收藏
页码:313 / 319
页数:7
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