Specialized pro-resolving lipid mediators in the inflammatory response: An update

被引:347
作者
Bannenberg, Gerard [3 ]
Serhan, Charles N. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Ctr Expt Therapeut & Reperfus Injury, Dept Anesthesiol Perioperat & Pain Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Harvard Inst Med 829, Boston, MA 02115 USA
[3] CSIC, Dept Plant Mol Genet, Ctr Nacl Biotecnol, Madrid, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2010年 / 1801卷 / 12期
基金
美国国家卫生研究院;
关键词
Anti-inflammatory; Apoptosis; Aspirin; Inflammation; Leukocyte; Lipid mediator; Protectin; Resolution; Resolvin; POLYUNSATURATED FATTY-ACIDS; TRIGGERED 15-EPI-LIPOXIN A(4); LIPOXIN A(4); DOCOSAHEXAENOIC ACID; ANTIINFLAMMATORY ACTIONS; HUMAN-NEUTROPHILS; LEUKOTRIENE B-4; APOPTOTIC NEUTROPHILS; VASCULAR-PERMEABILITY; ARACHIDONIC-ACID;
D O I
10.1016/j.bbalip.2010.08.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new genus of specialized pro-resolving mediators (SPM) which include several families of distinct local mediators (lipoxins, resolvins, protectins, and maresins) are actively involved in the clearance and regulation of inflammatory exudates to permit restoration of tissue homeostasis. Classic lipid mediators that are temporally regulated are formed from arachidonic acid, and novel local mediators were uncovered that are biosynthesized from omega-3 poly-unsaturated fatty acids, such as eicosapentaenoic acid, docosapentaenoic acid and docosahexaenoic acid. The biosynthetic pathways for resolvins are constituted by fatty acid lipoxygenases and cyclooxygenase-2 via transcellular interactions established by innate immune effector cells which migrate from the vasculature to inflamed tissue sites. SPM provide local control over the execution of an inflammatory response towards resolution, and include recently recognized actions of SPM such as tissue protection and host defense. The structural families of the SPM do not resemble classic eicosanoids (PC or LT) and are novel structures that function uniquely via pro-resolving cellular and molecular targets. The extravasation of inflammatory cells expressing SPM biosynthetic routes are matched by the temporal provision of essential fatty acids from circulation needed as substrate for the formation of SPM. The present review provides an update and overview of the biosynthetic pathways and actions of SPM, and examines resolution as an integrated component of the inflammatory response and its return to homeostasis via biochemically active resolution mechanisms. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1260 / 1273
页数:14
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