human neutrophil staining and preparation of neutrophil assay plate for live cell analysis

Dual-Dye Live Cell Analysis를 사용한 NET 형성 정량화

Neutrophil extracellular traps (NETs) are web-like chromatin structures extruded from neutrophils in response to various inflammatory stimuli. NETs are composed of DNA, histones, and various anti-microbial proteins/peptides, which trap and kill infectious pathogens and invoke inflammatory responses1.
While NETs are beneficial for host defense against pathogens, they have gathered attention as a potential driver of various autoimmune diseases2, thrombosis3, metabolic diseases4, and metastatic growth of cancers5. As such, inhibition of NET formation is a potential therapeutic option for these diseases. However, despite some promising NETs-targeting molecules in development6, there is still no approved therapy that specifically affects this mechanism. This is, at least partially, attributable to the lack of objective, unbiased, reproducible, and high throughput quantification methods for NET formation.
We established and reported a new method utilizing a dual-color live-cell imaging platform7,8. Time-lapse images of neutrophils stained with membrane-permeable nuclear dye and membrane-impermeable DNA dye are analyzed by the software, and the numbers of pre- and post-NET-forming neutrophils are counted at multiple time points. Since the integrity of the plasma membrane is lost during NET formation by the regulation of PKC&#945;-mediated Lamin B and CDK4/6-mediated Lamin A/C disassembly9, NET-forming neutrophils are stained by membrane-impermeable DNA dye while healthy neutrophils are not. This method overcomes the problems of previously reported techniques to quantify NET formation and provides unbiased, high-throughput, reproducible, and accurate NET quantification in an automated manner.

저자 스포트라이트: Quantifying Neutrophil Extracellular Traps in Disease and Drug Screening Using Dual-Color Live-Cell Imaging(이중 색상 생세포 이미징을 사용한 질병 및 약물 스크리닝에서 호중구 세포외 트랩 정량화)

인간 호중구에서 호중구 세포외 트랩 형성을 정량화하기 위한 실시간 고처리량 기법

Our research focuses on neutrophils, which are essential first responders in the immune system and play a significant role in various diseases. Over the past two decades, it has become clear that neutrophils contribute to the development of cancer, autoimmune diseases, and other inflammatory conditions by disrupting immunoregulation. This includes forming neutrophilic extracellular traps, nets, web-like structures that respond to inflammation and could be targeted for therapy in these diseases.However, despite some promising molecules targeting nets, in development there is still no approved therapy that specifically affects this mechanism. This is at least partially attributable to the lack of an objective, unbiased, reproducible, and high-throughput quantification method for net formation. Our protocol employs dual-color live cell imaging to analyze neutrophil behavior using membrane permeable and impermeable dyes for precise net formation tracking.This method distinguishes between net-forming and healthy neutrophils based on membrane integrity and provides clear differentiation of cell death types through morphological changes absorbed in phase contrast imaging. This method overcomes the problems of previously-reported techniques to quantify net formation and provides an efficient, reproducible, and accurate net quantification in an automated manner. This method will help in neutrophil-targeted drug development by giving the ability to screen multiple therapeutic targets against net formation in a high-throughput manner.

Watch this Scientific Journal Video about Human Neutrophil Staining and Preparation of Neutrophil Assay Plate for Live Cell Analysis at JoVE.com

인간 호중구 염색 및 살아있는 세포 분석을 위한 호중구 분석 플레이트 준비

인간 말초 혈액에서 호중구를 분리한 후 1.5밀리리터 원심분리 튜브의 RPMI 1640 배지에 재현탁시킵니다. 1.5 밀리리터의 호중구 현탁액에 1 마이크로리터의 막 투과성 적색 DNA 다이를 첨가하고 어둠 속에서 5분 동안 배양합니다. 호중구 현탁액을 2, 실온에서 5분 동안 500g으로 원심분리합니다.원심분리 후 펠릿 호중구가 들어 있는 튜브를 제거하고 상층액을 흡인합니다. 호중구를 1밀리리터의 RPMI에 재현탁시키고 다시 원심분리합니다. 마지막 세척 후 호중구를 RPMI 1밀리리터에 재현탁시킵니다.소량의 호중구 현탁액을 혈구계에 추가하고 현미경으로 계산합니다. RPMI를 사용하여 호중구 현탁액을 밀리리터당 1.5배의 10에서 5번째 호중구로 희석합니다. 1 내지 100 미리 희석된 막 불투과성 녹색 DNA 염료 4 마이크로리터를 1 밀리리터의 호중구 현탁액에 첨가합니다.웰당 100마이크로리터의 호중구 현탁액을 투명한 조직 배양 처리된 96웰 플레이트에 분주합니다. 억제제가 있거나 없는 자극 시약이 포함된 100마이크로리터의 RPMI를 각 웰에 추가합니다. 플레이트를 5% 이산화탄소 인큐베이터에 있는 살아있는 세포 분석 시스템에 넣습니다.

human-neutrophil-staining-preparation-neutrophil-assay-plate-for-live

Research

JoVE Journal

Immunology and Infection

Human Neutrophil Staining and Preparation of Neutrophil Assay Plate for Live Cell Analysis

107 조회수.  National Institutes of Health (NIH). 인간 말초 혈액에서 호중구를 분리한 후 1.5밀리리터 원심분리 튜브의 RPMI 1640 배지에 재현탁시킵니다. 1.5 밀리리터의 호중구 현탁액에 1 마이크로리터의 막 투과성 적색 DNA 다이를 첨가하고 어둠 속에서 5분 동안 배양합니다. 호중구 현탁액을 2, 실온에서 5분 동안 500g으로 원심분리합니다.원심분리 후 펠릿 호중구가 들어 있는 튜브를 제거하고 상층액을 흡인합니다. 호?...

비디오: 인간 호중구 염색 및 살아있는 세포 분석을 위한 호중구 분석 플레이트 준비

Real-Time High Throughput Technique to Quantify Neutrophil Extracellular Traps Formation in Human Neutrophils

Neutrophils are myeloid-lineage cells that form a crucial part of the innate immune system. The past decade has revealed additional key roles that neutrophils play in the pathogenesis of cancer, autoimmune diseases, and various acute and chronic inflammatory conditions by contributing to the initiation and perpetuation of immune dysregulation through multiple mechanisms, including the formation of neutrophil extracellular traps (NETs), which are structures crucial in antimicrobial defense. Limitations in techniques to quantify NET formation in an unbiased, reproducible, and efficient way have restricted our ability to further understand the role of neutrophils in health and diseases. We describe an automated, real-time, high-throughput method to quantify neutrophils undergoing NET formation using a live cell imaging platform coupled with a membrane permeability-dependent dual-dye approach using two different DNA dyes to image intracellular and extracellular DNA. This methodology is able to help assess neutrophil physiology and test molecules that can target NET formation.

We present an automated high-throughput method to quantify neutrophil extracellular traps (NETs) utilizing the live cell analysis system, coupled with a membrane permeability-dependent dual-dye approach.

Neutrophils are myeloid-lineage cells that form a crucial part of the innate immune system. The past decade has revealed additional key roles that ...

연구

면역학 및 감염병학

After isolating neutrophils from human peripheral blood, resuspend them in RPMI 1640 Medium in a 1.5 milliliter centrifuge tube. Add one microliter of membrane permeable red DNA die to 1.5 milliliters of neutrophil suspension and incubate in the dark for five minutes. Centrifuge the neutrophil suspension at 2, 500g for five minutes at room temperature.After centrifugation, remove the tube containing pelleted neutrophils and aspirate the supernatant. Resuspend the neutrophils in one milliliter of RPMI and centrifuge it again. After the last wash, resuspend the neutrophils in one milliliter of RPMI.Add a small volume of neutrophil suspension to the hemocytometer and count them under a microscope. Dilute the neutrophil suspension to 1.5 times 10 to the fifth neutrophils per milliliter using RPMI. Add four microliters of one to 100 pre-diluted membrane impermeable green DNA dye to the one milliliter of neutrophil suspension.Dispense 100 microliters of neutrophil suspension per well into a clear tissue culture treated 96 well plate. Add 100 microliters of RPMI containing stimulus reagents with or without inhibitor into the respective wells. Place the plate in a live cell analysis system housed in a 5%carbon dioxide incubator.

Scanning Plate Setup and Quantitative Analysis of Neutrophil Extracellular Traps Formation in Human Neutrophils

To begin, start the live cell analysis system software. Press the plus symbol at the top left corner of the screen to initiate the add vessel. Choose Scan on Schedule, then select New to run the scanning program.Select Standard. Then set scan settings as cell-by-cell options to None and image channels to Phase, Green, and Red, with respective acquisition times. Set objective to 20x.From the list, choose the plate and select the vessel location to put the plate on the tray of the imaging system. Select the wells containing samples and decide the number of images to capture per well. This information automatically generates an estimated scan duration for the plate.Click Create Plate Map to input information for each well, such as cell type and compound. Then name the study. On the next screen, select Basic Analyzer as the analysis type and choose Analysis Definition from the dropdown list, which shows previously used analysis definitions.Leave spectral unmixing for both green and red at 0.0. Schedule the scan to occur every 15 to 20 minutes for eight hours. Drag the white and gray bar on top of the screen to set the starting time of the scan.On the next screen, review the scan settings, and press Add to Schedule to start scanning. After scanning, on the View tab, open the vessel for analysis. Press Launch Analysis on the left of the screen and select Create New Analysis Definition.Choose Basic Analyzer and use Phase, Green, Red, and Overlap image channels. Select six to eight representative sample images for training. To configure the analysis definition, set green objects to neutrophils forming neutrophil extracellular traps or NETs, and red objects to the nuclei of all neutrophils.Press Preview Current or Preview All and adjust each parameter to optimize the results. Choose the scan times and wells for analysis. Then provide a label for the analysis definition.Review the summary and launch the analysis. After analysis, double click on the name of the analysis definition to open the analyzed study. Open Layers on the left of the screen and check if each cell is correctly marked.Click Graph Metrics on the left of the screen, then select count per image for green count. Choose the time points and wells to be exported. For select grouping, select Plate Map Replicates to confirm all wells are correctly specified during scanning, and click on Export Data.Similarly, export the data for red count and overlap count. Using the given equation, calculate the percentage of NETs forming cells for each condition and time point. The time course of the NET formation is visualized by plotting the percentage of NET-forming neutrophils at each time point.Adding an AKT inhibitor blocked the NET formation in neutrophils stimulated with PMA or calcium ionophore. Demonstrating the potential molecules targeting NET formation may be tested in a high throughput manner using this methodology.