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CXCL16/CXCR6 介导的人外周血单核细胞黏附至炎症内皮细胞。

CXCL16/CXCR6-mediated adhesion of human peripheral blood mononuclear cells to inflamed endothelium.

机构信息

Department of Clinical Pharmacology, University Hospital Frankfurt, Theodor-Stern-Kai 7, 60509 Frankfurt, Germany.

Department of Clinical Pharmacology, University Hospital Frankfurt, Theodor-Stern-Kai 7, 60509 Frankfurt, Germany.

出版信息

Cytokine. 2019 Oct;122:154081. doi: 10.1016/j.cyto.2017.06.008. Epub 2017 Jun 21.

Abstract

The endothelial chemokine CXC motif ligand 16 (CXCL16) is involved in the recruitment and firm adhesion of CXCR6 cells to the atherosclerosis-prone aortic vessel wall. Recently we showed that CXCR6 platelets from flowing blood attach to CXCL16 expressed by activated endothelium on the luminal side of the blood vessel. With this study we supplement these findings with the observation that platelets bound to the inflamed endothelium are presenting CXCR6 to CXCL16-positive peripheral blood mononuclear cells (PBMCs) and, thus, are mediating an increased adhesion of PBMCs to the arterial wall. Furthermore we identified endothelial CXCL16 as an important adhesion molecule promoting the firm adhesion of CXCR6-positive PBMCs to inflamed endothelium. Our results demonstrate that endothelial CXCL16 as well as platelet CXCR6 are acting as potent PBMC-adhesion ligands, inducing PBMC-adhesion to the atherosclerosis-prone vessel wall and thus promoting the progression of atherosclerosis.

摘要

内皮趋化因子 CXC 基元配体 16(CXCL16)参与募集和 CXCR6 细胞在动脉粥样硬化倾向的主动脉血管壁上的牢固黏附。最近我们发现,从血流中捕获的 CXCR6 血小板附着于血管腔侧激活的内皮细胞表达的 CXCL16。通过这项研究,我们补充了以下观察结果:与炎症内皮结合的血小板将 CXCR6 呈现给 CXCL16 阳性的外周血单核细胞(PBMC),从而介导 PBMC 与动脉壁的黏附增加。此外,我们鉴定出内皮 CXCL16 是一种重要的黏附分子,促进 CXCR6 阳性 PBMC 与炎症内皮的牢固黏附。我们的研究结果表明,内皮 CXCL16 以及血小板 CXCR6 均作为有效的 PBMC 黏附配体,诱导 PBMC 黏附于易发生动脉粥样硬化的血管壁,从而促进动脉粥样硬化的进展。

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