Feistritzer Clemens, Sturn Daniel H, Kaneider Nicole C, Djanani Angela, Wiedermann Christian J
Division of General Internal Medicine, Department of Internal Medicine, University of Innsbruck, Innsbruck, Austria.
J Allergy Clin Immunol. 2003 Aug;112(2):375-81. doi: 10.1067/mai.2003.1609.
Eosinophil infiltration is a characteristic feature of allergic inflammation. Allergic responses are associated with local activation of the coagulation pathway and accumulation of fibrin.
We tested whether protein C and activated protein C (APC), which are endogenous anti-inflammatory coagulation inhibitors, affect eosinophil function.
Eosinophils were from venous blood of healthy donors. Cell migration and apoptosis were studied by using micropore filter assays and fluorometry, respectively. Receptor expression was investigated by means of RT-PCR and SDS-PAGE of immunoprecipitated protein.
Protein C and APC had no significant chemotactic effects on eosinophils. Eosinophils pretreated with protein C or APC showed significantly reduced migration toward chemoattractants. No effect of either protein C preparation was seen in eosinophil apoptosis assays. The inhibiting effect on migration was reversed by an antibody against the endothelial protein C receptor (EPCR). Synthesis of EPCR by eosinophils is suggested by demonstration of receptor mRNA expression and detection of metabolically labeled receptor protein.
Data suggest that an EPCR is expressed by eosinophils whose activation with protein C or APC arrests directed migration. Protein C-affected eosinophil chemotaxis is a novel thrombin-independent component of the protein C pathway.
嗜酸性粒细胞浸润是变应性炎症的一个特征性表现。变应性反应与凝血途径的局部激活及纤维蛋白的积聚有关。
我们检测了作为内源性抗炎性凝血抑制剂的蛋白C和活化蛋白C(APC)是否影响嗜酸性粒细胞功能。
嗜酸性粒细胞取自健康供者的静脉血。分别采用微孔滤膜试验和荧光测定法研究细胞迁移和凋亡。通过RT-PCR和免疫沉淀蛋白的SDS-PAGE研究受体表达。
蛋白C和APC对嗜酸性粒细胞无明显趋化作用。用蛋白C或APC预处理的嗜酸性粒细胞对趋化因子的迁移明显减少。在嗜酸性粒细胞凋亡试验中未观察到任何一种蛋白C制剂的作用。抗内皮细胞蛋白C受体(EPCR)抗体可逆转对迁移的抑制作用。嗜酸性粒细胞中EPCR的合成通过受体mRNA表达的证实及代谢标记受体蛋白的检测得以提示。
数据表明嗜酸性粒细胞表达EPCR,蛋白C或APC对其激活可阻止定向迁移。蛋白C影响的嗜酸性粒细胞趋化性是蛋白C途径中一个新的不依赖凝血酶的成分。