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
相关论文
共 36 条
[21]   Inhibition of monocyte chemotaxis to C-C chemokines by antisense oligonucleotide for cytosolic phospholipase A(2) [J].
Locati, M ;
Lamorte, G ;
Luini, W ;
Introna, M ;
Bernasconi, S ;
Mantovani, A ;
Sozzani, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :6010-6016
[22]   Abnormalities in monocyte recruitment and cytokine expression in monocyte chemoattractant protein 1-deficient mice [J].
Lu, B ;
Rutledge, BJ ;
Gu, L ;
Fiorillo, J ;
Lukacs, NW ;
Kunkel, SL ;
North, R ;
Gerard, C ;
Rollins, BJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (04) :601-608
[23]   Role of the monocyte chemoattractant protein and eotaxin subfamily of chemokines in allergic inflammation [J].
Luster, AD ;
Rothenberg, ME .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 62 (05) :620-633
[24]   Identification of an intracellular receptor for lysophosphatidic acid (LPA):: LPA is a transcellular PPARγ agonist [J].
McIntyre, TM ;
Pontsler, AV ;
Silva, AR ;
St Hilaire, A ;
Xu, Y ;
Hinshaw, JC ;
Zimmerman, GA ;
Hama, K ;
Aoki, J ;
Arai, H ;
Prestwich, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (01) :131-136
[25]   iPLA2β :: front and center in human monocyte chemotaxis to MCP-1 [J].
Mishra, Ravi S. ;
Carnevale, Kevin A. ;
Cathcart, Martha K. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (02) :347-359
[26]   Potentiation of Ca2+ signaling in endothelial cells by 11,12-epoxyeicosatrienoic acid [J].
Mombouli, JV ;
Holzmann, S ;
Kostner, GM ;
Graier, WF .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1999, 33 (05) :779-784
[27]   Bioactive lysophospholipids and their G protein-coupled receptors [J].
Moolenaar, WH .
EXPERIMENTAL CELL RESEARCH, 1999, 253 (01) :230-238
[28]   Stable adhesion and migration of human neutrophils requires phospholipase D-mediated activation of the integrin CD11b/CD18 [J].
Powner, Dale J. ;
Pettitt, Trevor R. ;
Anderson, Rhodri ;
Nash, Gerard B. ;
Wakelam, Michael J. O. .
MOLECULAR IMMUNOLOGY, 2007, 44 (12) :3211-3221
[29]   Characterization of 5,6-and 8,9-epoxyeicosatrienoic acids (5,6-and 8,9-EET) as potent in vivo angiogenic lipids [J].
Pozzi, A ;
Macias-Perez, I ;
Abair, T ;
Wei, SZ ;
Su, Y ;
Zent, R ;
Falck, JR ;
Capdevila, JH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (29) :27138-27146
[30]  
RERICHA EC, 2007, SCI STKE, pPE40