血小板
内皮
止血
P2Y12
血小板活化
血小板粘附
细胞外基质
药理学
体外
替卡格雷
体内
内皮干细胞
受体拮抗剂
组胺
化学
受体
敌手
免疫学
医学
生物
内科学
生物化学
血小板聚集
阿司匹林
氯吡格雷
生物技术
作者
Alison Banka,Omolola Eniola‐Adefeso
出处
期刊:Platelets
[Informa]
日期:2021-12-20
卷期号:33 (5): 692-699
被引量:5
标识
DOI:10.1080/09537104.2021.1988550
摘要
In vitro flow assays utilizing microfluidic devices are often used to study human platelets as an alternative to the costly animal models of hemostasis and thrombosis that may not accurately represent human platelet behavior in vivo. Here, we present a tunable in vitro model to study platelet behavior in human whole blood flow that includes both an inflamed, damaged endothelium and exposed extracellular matrix. We demonstrate that the model is adaptable across various anticoagulants, shear rates, and proteins for endothelial cell culture without the need for a complicated, custom-designed device. Furthermore, we verified the ability of this 'damaged endothelium' model as a screening method for potential anti-platelet or anti-thrombotic compounds using a P2Y12 receptor antagonist (ticagrelor), a pan-selectin inhibitor (Bimosiamose), and a histamine receptor antagonist (Cimetidine). These compounds significantly decreased platelet adhesion to the damaged endothelium, highlighting that this model can successfully screen anti-platelet compounds that target platelets directly or the endothelium indirectly.
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