首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Pre-analytical and analytical variables affecting the measurement of plasma-derived microparticle tissue factor activity
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Pre-analytical and analytical variables affecting the measurement of plasma-derived microparticle tissue factor activity

机译:分析前和分析变量会影响血浆来源的微粒组织因子活性的测量

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Introduction: Elevated levels of tissue factor positive (TF +) microparticles (MPs) are observed in plasma from a variety of patients with an increased risk of thrombosis. We and others have described the measurement of TF activity in MPs isolated from plasma. The aim of this study was to investigate the effects of pre-analytical and analytical variables on TF activity of MPs isolated from blood of healthy volunteers either untreated or treated ex vivo with bacterial lipopolysaccharide. Materials and methods: We evaluated the following parameters: use of different centrifugation speeds to isolate the MPs; comparison of TF activity of MPs isolated from platelet poor plasma versus platelet free plasma; effect of freeze/thaw on MP TF activity; and comparison of the MP TF activity assay with the measurement of TF protein by ELISA or flow cytometry. Results: MPs prepared from platelet poor plasma by centrifugation at 20,000 × g or 100,000 × g for 15 minutes had similar levels of TF activity. However, significantly less TF activity was found in MPs isolated from platelet free plasma compared with platelet poor plasma. Interestingly, freeze/thawing of the plasma showed donor to donor variation in MP TF activity, with a moderate increase in some individuals. Conclusion: TF + MPs can be quantitatively isolated from platelet poor or platelet free plasma by centrifugation at 20,000 × g for 15 minutes. Measurement of MP TF activity in plasma may be used to detect a prothrombotic state in patients with various diseases.
机译:简介:在各种血栓形成风险增加的患者的血浆中,发现组织因子阳性(TF +)微粒(MPs)的水平升高。我们和其他人描述了从血浆中分离出的MP中TF活性的测量方法。这项研究的目的是研究分析前和分析变量对从健康志愿者血液中分离得到的MP的TF活性的影响,这些健康志愿者未经细菌多糖处理或离体处理。材料和方法:我们评估了以下参数:使用不同的离心速度分离MP。从贫血小板血浆与无血小板血浆分离的MP的TF活性比较;冻融对MP TF活性的影响; MP TF活性测定与通过ELISA或流式细胞仪测定TF蛋白的比较。结果:通过在20,000×g或100,000×g下离心15分钟从贫血小板血浆中制备的MP的TF活性水平相似。但是,与无血小板血浆相比,从无血小板血浆中分离出的MP中发现的TF活性明显较低。有趣的是,血浆的冷冻/解冻显示出MP TF活性的供体间变化,某些个体有中等程度的增加。结论:通过以20,000×g离心15分钟,可从贫血小板或无血小板血浆中定量分离TF + MPs。血浆MP TF活性的测量可用于检测患有各种疾病的患者的血栓前状态。

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