Spurgeon Benjamin E J, Frelinger Andrew L
Center for Platelet Research Studies, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.
Cytometry A. 2023 Dec;103(12):935-940. doi: 10.1002/cyto.a.24797. Epub 2023 Oct 3.
Using spectral flow cytometry, we developed a 16-color panel for analysis of platelet phenotype and function in human whole blood. The panel contains markers of clinical relevance and follows an optimized protocol for the high-parameter phenotyping of (phosphatidylserine positive) procoagulant platelets. Inclusion of established markers, such as CD62P and PAC-1, allows the subsetting of classic (proinflammatory and proaggregatory) phenotypes, while addition of novel markers, such as TLR9, allows the resolution of platelets with nonclassic functions. Multiple inducible (C3b, CD63, CD107a, CD154, and TLT-1) and constitutive (CD29, CD31, CD32, CD36, CD42a, CD61, and GPVI) markers are also measurable, and we demonstrate the use of automatic gating for platelet analysis. The panel is widely applicable to research and clinical settings and can be readily modified, should users wish to tailor the panel to more specific needs.
我们使用光谱流式细胞术开发了一个16色面板,用于分析人全血中血小板的表型和功能。该面板包含具有临床相关性的标志物,并遵循针对(磷脂酰丝氨酸阳性)促凝血血小板进行高参数表型分析的优化方案。纳入已确立的标志物,如CD62P和PAC-1,可对经典的(促炎和促聚集)表型进行亚群分析,而添加新型标志物,如TLR9,则可区分具有非经典功能的血小板。多种诱导性(C3b、CD63、CD107a、CD154和TLT-1)和组成性(CD29、CD31、CD32、CD36、CD42a、CD61和GPVI)标志物也可测量,并且我们展示了自动设门在血小板分析中的应用。该面板广泛适用于研究和临床环境,并且如果用户希望根据更具体的需求定制面板,它可以很容易地进行修改。