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活化的血小板通过CD40的连接诱导人脐静脉内皮细胞上组织因子的表达。

Activated platelets induce tissue factor expression on human umbilical vein endothelial cells by ligation of CD40.

作者信息

Slupsky J R, Kalbas M, Willuweit A, Henn V, Kroczek R A, Müller-Berghaus G

机构信息

Haemostasis Research Unit, Max-Planck-Institute for Physiological and Clinical Research, Kerckhoff-Klinik GmbH, Bad Nauheim, Germany.

出版信息

Thromb Haemost. 1998 Dec;80(6):1008-14.

PMID:9869175
Abstract

CD40 is a type I member of the tumour necrosis factor (TNF) receptor superfamily of proteins, and is present on a wide variety of cells including vascular endothelial cells. Ligation of this receptor on endothelial cells is known to increase expression of inflammatory adhesion molecules. We have recently demonstrated that platelets express the ligand of CD40 (CD154) within seconds of exposure to agonist, and interact with endothelial cells to participate directly in the induction of an inflammatory response. Here we show that activated platelets induce tissue factor (TF) expression on endothelial cells in a CD40/CD154-dependent manner, and that the magnitude of this response can equal that induced by TNFe. Moreover, CD40 ligation on endothelial cells downregulates the expression of thrombomodulin. We also show that CD40-mediated TF expression is less sensitive to inhibition with the oxidative radical scavenger pyrrolidine dithiocarbamate than is that mediated by TNFalpha, indicating that CD40 has a distinct signalling pathway. Tissue factor is a cell membrane protein which functions as the main trigger of the extrinsic pathway of blood coagulation, and its expression on endothelial cells is implicated in wound healing and angiogenesis. Since platelets are among the first cells involved in haemostasis following tissue injury, our data showing that ligation of CD40 by CD154 induces a procoagulant phenotype on vascular endothelial cells suggests that platelets may play an important role in the induction of wound healing.

摘要

CD40是肿瘤坏死因子(TNF)受体超家族蛋白中的I型成员,存在于包括血管内皮细胞在内的多种细胞上。已知内皮细胞上该受体的结合会增加炎症黏附分子的表达。我们最近证明,血小板在暴露于激动剂后数秒内就会表达CD40的配体(CD154),并与内皮细胞相互作用,直接参与炎症反应的诱导。在此我们表明,活化的血小板以CD40/CD154依赖的方式诱导内皮细胞上组织因子(TF)的表达,并且这种反应的程度可与TNFα诱导的程度相当。此外,内皮细胞上的CD40结合会下调血栓调节蛋白的表达。我们还表明,CD40介导的TF表达比TNFα介导的对氧化自由基清除剂吡咯烷二硫代氨基甲酸盐的抑制作用更不敏感,这表明CD40具有独特的信号通路。组织因子是一种细胞膜蛋白,作为血液凝固外源性途径的主要触发因子,其在内皮细胞上的表达与伤口愈合和血管生成有关。由于血小板是组织损伤后参与止血的首批细胞之一,我们的数据表明CD154与CD40的结合会在血管内皮细胞上诱导促凝表型,这表明血小板可能在伤口愈合的诱导中起重要作用。

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