Triggiani Massimo, Granata Francescopaolo, Giannattasio Giorgio, Marone Gianni
Division of Clinical Immunology and Allergy, Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.
J Allergy Clin Immunol. 2005 Nov;116(5):1000-6. doi: 10.1016/j.jaci.2005.08.011. Epub 2005 Oct 3.
Secretory phospholipases A(2) (sPLA(2)s) are molecules released in plasma and biologic fluids of patients with systemic inflammatory, autoimmune, and allergic diseases. Several sPLA(2) isoforms are expressed and released by such human inflammatory cells as neutrophils, eosinophils, basophils, T cells, monocytes, macrophages, and mast cells. Certain sPLA(2)s release arachidonic acid, thereby providing the substrate for the biosynthesis of proinflammatory eicosanoids. However, there are other mechanisms by which sPLA(2)s might participate in the synthesis of lipid mediators. Interestingly, sPLA(2)s activate inflammatory cells through mechanisms unrelated to their enzymatic activity. Several sPLA(2)s induce degranulation of mast cells and eosinophils and activate exocytosis in macrophages. Furthermore, sPLA(2)s promote cytokine and chemokine production from macrophages, neutrophils, eosinophils, monocytes, and endothelial cells. Some of these effects are mediated by the binding of sPLA(2)s to specific receptors expressed on effector cells. Thus sPLA(2)s might play important roles in the initiation and amplification of the inflammatory reaction. Selective inhibitors of sPLA(2)s and specific antagonists of sPLA(2) receptors might prove useful in the treatment of allergic and autoimmune diseases, such as bronchial asthma and rheumatoid arthritis.
分泌型磷脂酶A2(sPLA2)是在患有全身性炎症、自身免疫性疾病和过敏性疾病的患者的血浆和生物体液中释放的分子。几种sPLA2亚型由中性粒细胞、嗜酸性粒细胞、嗜碱性粒细胞、T细胞、单核细胞、巨噬细胞和肥大细胞等人炎症细胞表达并释放。某些sPLA2释放花生四烯酸,从而为促炎类二十烷酸的生物合成提供底物。然而,sPLA2可能通过其他机制参与脂质介质的合成。有趣的是,sPLA2通过与其酶活性无关的机制激活炎症细胞。几种sPLA2诱导肥大细胞和嗜酸性粒细胞脱颗粒,并激活巨噬细胞的胞吐作用。此外,sPLA2促进巨噬细胞、中性粒细胞、嗜酸性粒细胞、单核细胞和内皮细胞产生细胞因子和趋化因子。其中一些作用是由sPLA2与效应细胞上表达的特异性受体结合介导的。因此,sPLA2可能在炎症反应的启动和放大中发挥重要作用。sPLA2的选择性抑制剂和sPLA2受体的特异性拮抗剂可能被证明对治疗过敏性和自身免疫性疾病有用,如支气管哮喘和类风湿性关节炎。