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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Endothelial protein C receptor-dependent inhibition of migration of human lymphocytes by protein C involves epidermal growth factor receptor.
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Endothelial protein C receptor-dependent inhibition of migration of human lymphocytes by protein C involves epidermal growth factor receptor.

机译:内皮细胞对蛋白C受体的内皮细胞C受体迁移的抑制作用涉及表皮生长因子受体。

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摘要

The protein C pathway is an important regulator of the blood coagulation system. Protein C may also play a role in inflammatory and immunomodulatory processes. Whether protein C or activated protein C affects lymphocyte migration and possible mechanisms involved was tested. Lymphocyte migration was studied by micropore filter assays. Lymphocytes that were pretreated with protein C (Ceprotin) or activated protein C (Xigris) significantly reduced their migration toward IL-8, RANTES, MCP-1, and substance P, but not toward sphingosine-1-phosphate. The inhibitory effects of protein C or activated protein C were reversed by Abs against endothelial protein C receptor and epidermal growth factor receptor. Evidence for the synthesis of endothelial protein C receptor by lymphocytes is shown by demonstration of receptor mRNA expression and detection of endothelial protein C receptor immunoreactivity on the cells' surface. Data suggest that an endothelial protein C receptor is expressed by lymphocytes whose activation with protein C or activated protein C arrests directed migration. Exposure of lymphocytes to protein C or activated protein C stimulates phosphorylation of Tyr845 of epidermal growth factor receptor, which may be relevant for cytoprotective effects of the protein C pathway.
机译:蛋白C途径是血液凝固系统的重要调节剂。蛋白C在炎症和免疫调节过程中也可能起作用。蛋白C或活化的蛋白C是否影响淋巴细胞迁移,并测试了可能的机制。通过微孔滤器测定研究了淋巴细胞的迁移。用蛋白C(Ceprotin)或活化蛋白C(Xigris)预处理的淋巴细胞可显着减少其向IL-8,RANTES,MCP-1和P物质的迁移,但不会向1-磷酸鞘氨醇迁移。 Abs逆转了蛋白C或活化蛋白C对内皮蛋白C受体和表皮生长因子受体的抑制作用。通过证明受体mRNA的表达和在细胞表面检测内皮蛋白C受体的免疫反应性,可以证明淋巴细胞合成了内皮蛋白C受体的证据。数据表明内皮蛋白C受体是由淋巴细胞表达的,淋巴细胞被蛋白C激活或激活的蛋白C阻止了定向迁移。淋巴细胞暴露于蛋白C或活化的蛋白C会刺激表皮生长因子受体的Tyr845磷酸化,这可能与蛋白C途径的细胞保护作用有关。

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