Rebernick Ryan, Fahmy Lauren, Glover Christopher, Bawadekar Mandar, Shim Daeun, Holmes Caitlyn L, Rademacher Nicole, Potluri Hemanth, Bartels Christie M, Shelef Miriam A
1Department of Medicine, University of Wisconsin, Madison, WI USA.
2Department of Pathology & Laboratory Medicine, University of Wisconsin, Madison, WI USA.
Biol Proced Online. 2018 Apr 1;20:7. doi: 10.1186/s12575-018-0072-y. eCollection 2018.
Neutrophil extracellular traps (NETs), extracellular structures composed of decondensed chromatin and antimicrobial molecules, are released in a process called NETosis. NETs, which are part of normal host defense, have also been implicated in multiple human diseases. Unfortunately, methods for quantifying NETs have limitations which constrain the study of NETs in disease. Establishing optimal methods for NET quantification holds the potential to further elucidate the role of NETs in normal and pathologic processes.
To better quantify NETs and NET-like structures, we created DNA Area and NETosis Analysis (DANA), a novel ImageJ/Java based program which provides a simple, semi-automated approach to quantify NET-like structures and DNA area. DANA can analyze many fluorescent microscope images at once and provides data on a per cell, per image, and per sample basis. Using fluorescent microscope images of Sytox-stained human neutrophils, DANA quantified a similar frequency of NET-like structures to the frequency determined by two different individuals counting by eye, and in a fraction of the time. As expected, DANA also detected increased DNA area and frequency of NET-like structures in neutrophils from subjects with rheumatoid arthritis as compared to control subjects. Using images of DAPI-stained murine neutrophils, DANA (installed by an individual with no programming background) gave similar frequencies of NET-like structures as the frequency of NETs determined by two individuals counting by eye. Further, DANA quantified more NETs in stimulated murine neutrophils compared to unstimulated, as expected.
DANA provides a means to quantify DNA decondensation and the frequency of NET-like structures using a variety of different fluorescent markers in a rapid, reliable, simple, high-throughput, and cost-effective manner making it optimal to assess NETosis in a variety of conditions.
中性粒细胞胞外诱捕网(NETs)是由解聚的染色质和抗菌分子组成的细胞外结构,在一种称为NETosis的过程中释放。NETs作为正常宿主防御的一部分,也与多种人类疾病有关。不幸的是,NETs的定量方法存在局限性,这限制了在疾病中对NETs的研究。建立最佳的NET定量方法有可能进一步阐明NETs在正常和病理过程中的作用。
为了更好地定量NETs和NET样结构,我们创建了DNA面积和NETosis分析(DANA),这是一个基于ImageJ/Java的新型程序,它提供了一种简单的半自动方法来定量NET样结构和DNA面积。DANA可以一次分析许多荧光显微镜图像,并提供每个细胞、每个图像和每个样本的数据。使用Sytox染色的人类中性粒细胞的荧光显微镜图像,DANA定量的NET样结构频率与两名不同的人员通过肉眼计数确定的频率相似,而且所用时间仅为其一小部分。正如预期的那样,与对照受试者相比,DANA还检测到类风湿性关节炎患者中性粒细胞中DNA面积增加和NET样结构频率增加。使用DAPI染色的小鼠中性粒细胞图像,DANA(由一名没有编程背景的人员安装)给出的NET样结构频率与两名人员通过肉眼计数确定的NETs频率相似。此外,正如预期的那样,与未刺激的小鼠中性粒细胞相比,DANA在刺激的小鼠中性粒细胞中定量到更多的NETs。
DANA提供了一种手段,能够以快速、可靠、简单、高通量和具有成本效益的方式,使用多种不同的荧光标记物来定量DNA解聚和NET样结构的频率,使其成为在各种条件下评估NETosis的最佳选择。