Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
University of Cincinnati College of Medicine, Cincinnati, Ohio.
Curr Protoc. 2023 Feb;3(2):e668. doi: 10.1002/cpz1.668.
Platelets play a critical role in hemostasis and thrombosis; therefore, in vitro assays that measure platelet reactivity are fundamental tools to gain insight into these physiologic processes, to diagnose platelet disorders, and to develop antithrombotic therapies. However, conventional platelet assays such as aggregometry, the clinical gold standard for assessing platelet function, are low throughput and require specialized equipment. Since platelets have a finite life span ex vivo, processes to miniaturize and multiplex assays allow a much broader overview of platelet function in significantly less time than conventional assays. Several groups have developed simplified, high-throughput approaches to quantify platelet activation with standard laboratory equipment to lower the barrier of entry to study platelet biology. This article describes a panel of optimized and validated high-throughput microplate assays to comprehensively assess platelet functionality, independently or in combination, to increase throughput and reduce costs. Specifically, following stimulation of platelets, a plate reader can be used to measure light transmission aggregation via absorbance; dense-granule secretion based on ATP-dependent luminescence generation; and cytosolic calcium levels with a cell-permeant, fluorescent Ca -sensitive dye. Additionally, platelets are an easily accessible component of the blood that share signaling pathways with other cells, making them ideal for high-throughput drug screens. The highly adaptable and complementary assays presented in this article can be used to decipher the molecular mechanism underlying platelet activation or to identify novel inhibitors. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Microtiter plate-based light transmission aggregometry Basic Protocol 2: Measuring dense-granule secretion in high-throughput microplate assays Basic Protocol 3: Microtiter plate-based calcium mobilization Support Protocol: Platelet isolation and enumeration.
血小板在止血和血栓形成中起着关键作用;因此,测量血小板反应性的体外检测是深入了解这些生理过程、诊断血小板疾病和开发抗血栓治疗的基本工具。然而,传统的血小板检测方法,如聚集测定法,是评估血小板功能的临床金标准,但其通量较低,需要专门的设备。由于血小板在体外的寿命有限,因此将检测方法小型化和多重化的过程可以在比传统检测方法显著更短的时间内,更广泛地了解血小板功能。已经有几个小组开发了简化、高通量的方法来定量血小板激活,使用标准实验室设备降低研究血小板生物学的门槛。本文描述了一组优化和验证的高通量微板检测方法,可综合评估血小板功能,独立或组合使用,以提高通量并降低成本。具体来说,在血小板被刺激后,可以使用平板读数仪通过吸光度测量透光性聚集;基于 ATP 依赖性发光产生的致密颗粒分泌;以及使用细胞通透性的荧光 Ca2+敏感染料测量细胞内钙离子水平。此外,血小板是血液中易于获得的成分,与其他细胞共享信号通路,使其成为高通量药物筛选的理想选择。本文介绍的高度适应性和互补的检测方法可用于解析血小板激活的分子机制或识别新的抑制剂。© 2023 作者。Wiley 期刊出版公司出版的《当代协议》 Basic Protocol 1:微滴定板光传输聚集测定法 Basic Protocol 2:高通量微板测定法测定致密颗粒分泌 Basic Protocol 3:微滴定板钙动员测定法 支持方案:血小板分离和计数。