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癌症微泡在体外诱导内皮细胞中组织因子相关的促凝活性。

Cancer microvesicles induce tissue factor-related procoagulant activity in endothelial cells in vitro.

作者信息

Adesanya Mufuliat Adeola, Maraveyas Anthony, Madden Leigh A

机构信息

aHull York Medical School, University of Hull, Hull; University of York, York bSchool of Life Sciences, University of Hull, Hull, UK.

出版信息

Blood Coagul Fibrinolysis. 2017 Jul;28(5):365-372. doi: 10.1097/MBC.0000000000000607.

Abstract

: Microvesicles associated with tissue factor (TF) may play a role in cancer-related venous thromboembolism; however, not much is known about their interaction with the tumour stroma, especially the endothelium or any procoagulant changes seen because of this interaction. Using a head and neck squamous cell carcinoma line (UMSCC81B) and human umbilical vein endothelial cells (HUVECs), this study explored the interaction of cancer microvesicles released into cell culture media with endothelial cells in vitro, and assessed the procoagulant activity resulting from this interaction. Cell-free media containing UMSCC81B cancer microvesicles supported coagulation in a concentration-dependent manner, suggesting TF and microvesicle presence, this media was then added to HUVECs and flow cytometry analysis showed a subpopulation of HUVECs that had acquired a significantly high expression of TF, which was dependent upon the concentration of UMSCC81B media containing microvesicles present and confocal microscopy confirmed HUVECs associated with labelled microvesicles. The range of TF-positive HUVECs was determined to be 0, 4.2(±1.4), 12.5(±3.72), and 45.9(±18.7)% for microvesicle-positive media concentration of 0, 25, 50, and 100%, respectively, which resulted in decreasing prothrombin values of more than 600 (no clot), 126.4, 65.8, and 47.8 s. Our results demonstrate that procoagulant microvesicles shed by UMSCC81B induced a procoagulant effect in HUVECs through increased clotting activity and cell membrane surface expression of TF.

摘要

与组织因子(TF)相关的微泡可能在癌症相关的静脉血栓栓塞中起作用;然而,关于它们与肿瘤基质的相互作用,尤其是与内皮细胞的相互作用,或者由于这种相互作用而出现的任何促凝变化,我们了解得并不多。本研究使用头颈部鳞状细胞癌系(UMSCC81B)和人脐静脉内皮细胞(HUVECs),探讨了释放到细胞培养基中的癌症微泡与内皮细胞在体外的相互作用,并评估了这种相互作用产生的促凝活性。含有UMSCC81B癌症微泡的无细胞培养基以浓度依赖的方式支持凝血,表明存在TF和微泡,然后将该培养基添加到HUVECs中,流式细胞术分析显示有一部分HUVECs获得了显著高表达的TF,这取决于存在的含有微泡的UMSCC81B培养基的浓度,共聚焦显微镜证实了HUVECs与标记的微泡相关。对于微泡阳性培养基浓度分别为0、25、50和100%,TF阳性HUVECs的范围分别确定为0、4.2(±1.4)、12.5(±3.72)和45.9(±18.7)%,这导致凝血酶原值分别下降超过600(无凝块)、126.4、65.8和47.8秒。我们的结果表明,UMSCC81B释放的促凝微泡通过增加凝血活性和TF的细胞膜表面表达,在HUVECs中诱导了促凝作用。

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