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分泌型磷脂酶A2对人炎症细胞的激活作用。

Activation of human inflammatory cells by secreted phospholipases A2.

作者信息

Triggiani Massimo, Granata Francescopaolo, Frattini Annunziata, Marone Gianni

机构信息

Division of Clinical Immunology and Allergy, Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Via Pansini 5, Italy.

出版信息

Biochim Biophys Acta. 2006 Nov;1761(11):1289-300. doi: 10.1016/j.bbalip.2006.07.003. Epub 2006 Jul 21.

Abstract

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 sPLA(2)s are expressed and released by human inflammatory cells, such as neutrophils, eosinophils, T cells, monocytes, macrophages and mast cells. sPLA(2)s generate arachidonic acid and lysophospholipids thus contributing to the production of bioactive lipid mediators in inflammatory cells. However, sPLA(2)s also activate human inflammatory cells by mechanisms unrelated to their enzymatic activity. Several human and non-human sPLA(2)s 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 sPLA(2) receptors are current being tested for pharmacological treatment of inflammatory and autoimmune diseases.

摘要

分泌型磷脂酶A2(sPLA2)是在患有各种炎症、自身免疫和过敏性疾病患者的血清及生物体液中检测到的酶。sPLA2的不同亚型由人类炎症细胞表达并释放,如中性粒细胞、嗜酸性粒细胞、T细胞、单核细胞、巨噬细胞和肥大细胞。sPLA2生成花生四烯酸和溶血磷脂,从而促进炎症细胞中生物活性脂质介质的产生。然而,sPLA2也通过与其酶活性无关的机制激活人类炎症细胞。几种人类和非人类的sPLA2可诱导肥大细胞、中性粒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,一些(但不是全部)sPLA2亚型可促进巨噬细胞、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。这些效应主要是通过sPLA2与效应细胞上表达的特定膜靶点(硫酸乙酰肝素蛋白聚糖、M型、N型或甘露糖受体)结合介导的。因此,sPLA2可能通过至少两种机制在炎症反应的启动和放大中发挥重要作用:脂质介质的产生和炎症细胞的直接激活。目前正在测试sPLA2酶活性的选择性抑制剂和sPLA2受体的特异性拮抗剂用于炎症和自身免疫性疾病的药物治疗。

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