Activation of human inflammatory cells by secreted phospholipases A2

被引:90
作者
Triggiani, Massimo [1 ]
Granata, Francescopaolo [1 ]
Frattini, Annunziata [1 ]
Marone, Gianni [1 ]
机构
[1] Univ Naples Federico II, Div Clin Immunol & Allergy, CISI, I-80131 Naples, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2006年 / 1761卷 / 11期
关键词
secreted PLA(2); inflammation; cytokine; chemokine; signal transduction;
D O I
10.1016/j.bbalip.2006.07.003
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
Secreted phospholipases A(2) (sPLA(2)s) are enzymes detected in serum and biological fluids of patients with various inflammatory, autoimmune and allergic disorders. Different isoforms of sPLA2s are expressed and released by human inflammatory cells, such as neutrophils, eosinophils, T cells, monocytes, macrophages and mast cells. sPLA(2)c generate arachidonic acid and lysophospholipids thus contributing to the production of bioactive lipid mediators in inflammatory cells. However, sPLA2s also activate human inflammatory cells by mechanisms unrelated to their enzymatic activity. Several human and non-human sPLA(2)c induce degranulation of mast cells, neutrophils and eosinophils and activate exocytosis in macrophages. In addition some, but not all, sPLA(2) isoforms promote cytokine and chemokine production from macrophages, neutrophils, eosinophils, monocytes, and endothelial cells. These effects are primarily mediated by binding of sPLA(2)s to specific membrane targets (heparan sulfate proteoglycans, M-type, N-type or mannose receptors) expressed on effector cells. Thus, sPLA(2)s may play an important role in the initiation and amplification of inflammatory reactions by at least two mechanisms: production of lipid mediators and direct activation of inflammatory cells. Selective inhibitors of sPLA(2)-enzymatic activity and specific antagonists of sPLA2 receptors are current being tested for pharmacological treatment of inflammatory and autoimmune diseases. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1289 / 1300
页数:12
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