Markey Kate A, Gartlan Kate H
Memorial Sloan Kettering Cancer Center, New York, New York.
QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Curr Protoc Immunol. 2019 Jun;125(1):e72. doi: 10.1002/cpim.72. Epub 2019 Mar 6.
This unit describes methods for quantifying phagocytosis and imaging the immunological synapse between T cells and antigen-presenting cells (APCs), with both techniques delivering valuable information about APC function. These aspects of APC biology have traditionally been challenging to quantify, and imaging flow cytometry, which harnesses the high-throughput nature of flow cytometry combined with the capacity of microscopy to deliver spatial localization, facilitates analysis of these APC functions in a fashion that was previously not possible. Imaging flow cytometry allows large numbers of events to be captured and large amounts of fluorescence data to be quantified at the physical location of markers of interest, both on the cell surface and in intracellular compartments, combining key features of traditional flow cytometry and fluorescence microscopy. © 2019 by John Wiley & Sons, Inc.
本单元介绍了定量吞噬作用以及对T细胞与抗原呈递细胞(APC)之间免疫突触进行成像的方法,这两种技术都能提供有关APC功能的有价值信息。APC生物学的这些方面传统上难以定量,而成像流式细胞术利用了流式细胞术的高通量特性以及显微镜提供空间定位的能力,以前所未有的方式促进了对这些APC功能的分析。成像流式细胞术能够在感兴趣标记物的物理位置(包括细胞表面和细胞内区室)捕获大量事件并对大量荧光数据进行定量,结合了传统流式细胞术和荧光显微镜的关键特征。© 2019约翰威立国际出版公司。