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趋化因子受体CXCR4和CXCR7在血小板功能中的作用。

Role of chemokine receptors CXCR4 and CXCR7 for platelet function.

作者信息

Chatterjee Madhumita, Rath Dominik, Gawaz Meinrad

机构信息

Innere Medizin III, Kardiologie und Kreislauferkrankungen, Eberhard Karls Universität, 72076 Tübingen, Germany

Innere Medizin III, Kardiologie und Kreislauferkrankungen, Eberhard Karls Universität, 72076 Tübingen, Germany.

出版信息

Biochem Soc Trans. 2015 Aug;43(4):720-6. doi: 10.1042/BST20150113. Epub 2015 Aug 3.

Abstract

Platelet-derived SDF-1α (stromal cell derived factor-α) mediates inflammation, immune defence and repair mechanisms at site of tissue injury. This review summarizes the relative expression of CXC chemokine receptor 4 (CXCR4) and CXCR7 in platelets, their dynamic trafficking in presence of ligands like chemokine C-X-C-motif ligand 11 (CXCL11), CXCL12 and MIF (macrophage migration inhibitory factor); how these receptors differentially mediate the functional and survival response to the chemokines CXCL11, CXCL12 and MIF. We further elaborate and emphasize the prognostic significance of platelet surface expression of CXCR4-CXCR7 in the context of coronary artery disease (CAD). SDF-1α/CXCL12, CXCL11, MIF effects mediated through CXCR4 and CXCR7 may play a regulatory role at the site of vascular and tissue inflammation, immune defence and repair where activated platelets reach as forerunners and function as critical players.

摘要

血小板衍生的基质细胞衍生因子-1α(SDF-1α)介导组织损伤部位的炎症、免疫防御和修复机制。本综述总结了CXC趋化因子受体4(CXCR4)和CXCR7在血小板中的相对表达、它们在趋化因子C-X-C基序配体11(CXCL11)、CXCL12和巨噬细胞迁移抑制因子(MIF)等配体存在时的动态转运;这些受体如何差异地介导对趋化因子CXCL11、CXCL12和MIF的功能和存活反应。我们进一步阐述并强调了在冠状动脉疾病(CAD)背景下血小板表面CXCR4-CXCR7表达的预后意义。通过CXCR4和CXCR7介导的SDF-1α/CXCL12、CXCL11、MIF效应可能在血管和组织炎症、免疫防御及修复部位发挥调节作用,在这些部位,活化的血小板作为先驱者到达并发挥关键作用。

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