Signal-activated phospholipase regulation of leukocyte chemotaxis

被引:30
作者
Cathcart, Martha K. [1 ,1 ,2 ]
机构
[1] Lerner Res Inst, Dept Mol Med, Cleveland, OH 44195 USA
[2] Cleveland Clin, Lerner Coll Med, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
chronic inflammation; macrophage; lipid mediators; monocyte; HUMAN MONOCYTE CHEMOTAXIS; LOW-DENSITY-LIPOPROTEIN; ENDOTHELIAL-CELLS; EPOXYEICOSATRIENOIC ACIDS; CHEMOATTRACTANT PROTEIN-1; LYSOPHOSPHATIDIC ACID; LIPID OXIDATION; A(2); INHIBITION; PATHWAYS;
D O I
10.1194/jlr.R800096-JLR200
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
Signal-activated phospholipases are a recent focus of the rapidly growing field of lipid signaling. The extent of their impact on the pathways regulating diverse cell functions is beginning to be appreciated. A critical step in inflammation is the attraction of leukocytes to injured or diseased tissue. Chemotaxis of leukocytes, a requisite process for monocyte and neutrophil extravasation from the blood into tissues, is a critical step for initiating and maintaining inflammation in both acute and chronic settings. Recent studies have identified new important and required roles for two signal-activated phospholipases A(2) (PLA(2)) in regulating chemotaxis. The two intracellular phospholipases, cPLA(2)alpha (Group IVA) and iPLA(2)beta (Group VIA), act in parallel to provide distinct lipid mediators at different intracellular sites that are both required for leukocytes to migrate toward the chemokine monocyte chemoattractant protein-1. jlr This review will summarize the separate roles of these phospholipases as well as what is currently known about the influence of two other classes of intracellular signal-activated phospholipases, phospholipase C and phospholipase D, in regulating chemotaxis in eukaryotic cells, but particularly in human monocytes. The contributions of these phospholipases to chemotaxis both in vitro and in vivo will be highlighted.-Cathcart, M. K. Signal-activated phospholipase regulation of leukocyte chemotaxis. J. Lipid Res. 2009. S231-S236.
引用
收藏
页码:S231 / S236
页数:6
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