Live Imaging and Quantification of Neutrophil Extracellular Trap Formation

被引:4
|
作者
Silva, Lakmali Munasinghage [1 ,2 ]
Moutsopoulos, Niki [2 ]
Bugge, Thomas H. [1 ]
Doyle, Andrew [3 ,4 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Proteases & Tissue Remodeling Sect, NIH, Bethesda, MD USA
[2] Natl Inst Dent & Craniofacial Res, Oral Immun & Inflammat Sect, NIH, Bethesda, MD USA
[3] Natl Inst Dent & Craniofacial Res, NIDCR Imaging Core, NIH, Bethesda, MD USA
[4] Natl Inst Dent & Craniofacial Res, Cell Biol Sect, NIH, Bethesda, MD USA
来源
CURRENT PROTOCOLS | 2021年 / 1卷 / 07期
关键词
automated quantification; live imaging; neutrophil extracellular trap;
D O I
10.1002/cpz1.157
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
NeutrophilExtracellular Trap (NET) formation (NETosis) is a unique process that occurs in response to numerous stimuli. To investigate NETosis, we created a method that can be used easily without the need for complex programming abilities and commercial software packages. This article describes a fully automated assay to quantify NETosis using fluorescence live imaging on an automated widefield inverted microscope. Herein, we describe (1) sample preparation, (2) required equipment for automated acquisition, and finally (3) analysis of NETosis using the readily available image analysis software Fiji (ImageJ2). This protocol can be adapted to evaluate NETosis after different stimuli, and can be easily modified to allow high-throughput acquisition and analysis using a multi-well plate format. Published 2021. This article is a U.S. Government work and is in the public domain in the USA. Current Protocols published by Wiley Periodicals LLC.
引用
收藏
页数:21
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