Name: visualizing macrophage extracellular traps using confocal microscopy
Uploaded: 2017-10-19T14:00:00.000+00:00
Duration: 9 min 14 s
Description: Watch this Scientific Journal Video about Visualizing Macrophage Extracellular Traps Using Confocal Microscopy at JoVE.com

This work was funded by grants from Monash University, the National Health and Medical Research Council, and the Monash Lung and Sleep Institute. The authors would like to thank the staff of Clinical Immunology at Monash Health, Judy Callaghan, Alex Fulcher, Kirstin Elgass, and Camden Lo of Monash Micro Imaging (MMI) for help with the confocal microscopy imaging, and the authors acknowledge the MMI facilities of Monash University. The authors acknowledge the facilities, and scientific and technical assistance of the Monash Histology Platform.

This protocol follows experiments approved in: (1) humans by the Ethics Committee of Monash Medical Centre, and (2) animals by the Ethics Committee of the University of Melbourne.
1. Bronchoalveolar Lavage (BAL) Macrophages
<ol>
	<li>Use BAL to obtain lung macrophages in: (1) human subjects by bronchoscopy6, and (2) mice by using intra-tracheal aspiration13. 
	NOTE: Acquisition of the macrophages generally causes some activation of these cells. Macrophages are obtained from patients who require a bronchoscopy to investigate a potential medical problem and not all subjects may be suitable for analysis of METs (this will need to be determined for each individual project).
	<ol>
		<li>Take the BAL solution and spin down (500 x g for 10 min) to form a pellet, wash twice with culture medium (Roswell Park Memorial Institute Medium (RPMI) with 5% fetal calf serum and 1% L-glutamine) at room temperature, and then dilute cells in 4 mL of culture medium.</li>
		<li>If necessary, request a formal differential count; most of the cells (generally &#62;80%) will be macrophages6. 
		NOTE: This will generally be performed by a clinical histology service using the morphologic appearance of the different cells types6.</li>
		<li>Perform a viable macrophage cell count on the BAL solution using Trypan blue exclusion and a hemocytometer. 
		NOTE: BAL solution is obtained from humans and mice as mentioned in step 1.1.</li>
		<li>Add 1 - 4 x 105 macrophages to 24-well plates on coverslips in 500 &#181;L of culture medium per well and leave overnight at 37&#176;C; the cells will adhere to the coverslips. For human samples, add antibiotics (e.g., penicillin and streptomycin, 104 U/mL) to prevent bacterial contamination.</li>
	</ol>
	</li>
</ol>
2. Immunofluorescence Labeling/Microscopy of BAL Macrophages
NOTE: Cells are adhered onto coverslips as mentioned above.
<ol>
	<li>Remove the culture medium and wash the cells once with phosphate buffered saline (PBS). Fix cells in 2% paraformaldehyde/periodate/lysine (PLP) fixative for 10 min.</li>
	<li>Wash cells briefly in PBS, and then permeabilize in 0.2% Tween 20 in PBS for 20 min.</li>
	<li>Block cells with 10% chicken sera in 5% bovine serum albumin (BSA) diluted in PBS for 30 min.</li>
	<li>Incubate with primary and isotype control antibodies for 1 h at room temperature at 1:100 concentrations (more specific details are listed in Table of Materials) at 37 &#176;C. 
	NOTE: For the BAL samples, a specific marker of macrophages is usually not required.</li>
	<li>After the addition of primary antibodies, wash the cells in PBS, and further incubate with the corresponding secondary antibodies for 40 min at room temperature.</li>
	<li>Wash the sections in PBS and mount with DAPI-based mounting medium for visualization using a confocal microscope (as mentioned above) at laser excitations 405, 488, 561 and 647 nm and a 40X, 1.0 NA oil objective.</li>
</ol>
3. Lung Tissue Samples
NOTE: For in vivo studies of lung tissue, study the samples after the relevant exposure (e.g., as described by O&#39;Sullivan et al.7). The exposure that is most relevant for this experiment are infectious microorganisms, particularly bacteria. Mouse strains that could be used for this method are C57BL/6 or BALB/c mice, 10 - 12 weeks old, weight 25 - 30 g, and male.
<ol>
	<li>Euthanize mice, via an intraperitoneal injection of ketamine (400 mg/kg) and xylazine (40 mg/kg). Open the thoracic cavity and expose the lungs and heart using surgical forceps and scissors.
	<ol>
		<li>Infuse warm PBS using a 21-gauge needle into the right ventricle to wash out the blood from the vessels for 30 s, then infuse 10 mL of 2% PLP fixative for 30 s (into the right ventricle).</li>
		<li>Use warm PBS (42 &#176;C) to lavage the open chest cavity. Intubate the trachea with a 21-gauge needle and a piece of 0.8 mm tubing cut to size, and inject 800 &#181;L of pre-warmed (to 42 &#176;C), low-melting point 3% agarose solution.</li>
		<li>Tie off the trachea with braided silk (4.0 USP). Place the thread around the trachea, just below the insertion point of the cannula, and secure it via a simple overhand knot. To solidify the agarose, administer ice-cold PBS around the lungs. Remove the lungs and heart as a block from the thoracic cavity using both scissors and blunt dissection. Remove each lung individually and then fix them for 16 h in 2% PLP or formalin at 4 &#176;C.</li>
		<li>Store the specimens in PBS at 4 &#176;C until tissue sectioning. These methods for obtaining lung tissue have been previously described13.</li>
	</ol>
	</li>
	<li>To prepare the lung tissue samples use the following steps.
	<ol>
		<li>Fix lung tissues (resected in step 3.1) tissue in 10% natural-buffered formalin for 24 h at room temperature. Transfer to 75% ethanol and put in a tissue processor on a 12 h cycle, (2.5 h in 75% EtOH, 3 h in absolute EtOH, 3.5 h in solvent 3B, and for 3 h in paraffin).</li>
		<li>Embed in standard paraffin to create formalin-fixed, paraffin-embedded (FFPE) blocks which are stored at room temperature. 
		NOTE: At this stage, it is generally convenient to cut the lung sections for standard slides.</li>
		<li>Cut the FFPE lung sections at 4 - 5 &#181;m thickness using a microtome and mount on charged, coated slides as previously described by O&#39;Sullivan et al.7</li>
		<li>To mount slides, put 3 drops of mounting medium on 60 mm x 24 mm coverslips (size 1.5), invert the slide on the coverslip and push out excess medium. Hermetically seal with nail polish and store at room temperature.</li>
	</ol>
	</li>
</ol>
4. Preparation/Microscopy of Lung Tissue Samples
<ol>
	<li>To de-wax, rehydrate and pretreat the FFPE lung tissue sample with antigen retrieval solution.
	<ol>
		<li>Oven dry the FFPE slides for 60 min at 60 &#176;C. Then put the slides in xylene solution for 30 min and transfer to 70% ethanol solution for 5 min at room temperature. Rinse in tap water.</li>
		<li>Place in heat-proof plastic wrap and subject to HIER-antigen retrieval in a pressure cooker for 10 min in 10 m/mol/L Tris, 1 mmol/EDTA pH 9.0. Cool for 20 min. Wash twice in tap water for 5 min on a rocker, then once with PBS on rocker.</li>
		<li>Block with 10% chicken serum in 5% BSA/PBS for 30 min at room temperature.</li>
	</ol>
	</li>
	<li>Stain the tissue.
	<ol>
		<li>To define METs in macrophages, add primary antibodies (MMP-9, H3Cit, and F4/80) in 1% BSA/PBS for 16 h at 4 &#176;C at 1/100 dilution (specific details about antibody amounts are listed in Table of Materials). Wash two times with PBS for 5 min on a rocker.</li>
		<li>Achieve fluorescent detection by incubation with corresponding secondary antibodies in 1% BSA/PBS for 40 min at room temperature. Antibodies are: (1) chicken anti-mouse 488 (green), (2) chicken anti-goat 594 (red), and (3) donkey anti-mouse 647 (far red).</li>
		<li>Wash the sections in PBS and mount with DAPI-containing mounting medium for chromatin staining.</li>
	</ol>
	</li>
	<li>Obtain fluorescent images using a confocal laser scanning head attached to an inverted microscope.
	<ol>
		<li>Excite the preparation with 405, 488, 561, and 647 nm lasers. Capture single plane 512 x 512-pixel images by clicking on the line-sequential, leveling button (2 line averaging) using 20X&#160;0.1 NA air and 40X&#160;1.0 NA oil objectives.</li>
		<li>Obtain at least ten fields of view per section for analysis and data for each result (i.e., 10 high-power fields of view (HFOV) for the control, 10 for the stimulated sample, etc., for each mouse). 
		NOTE: To obtain a representative sample of the whole field, a matrix system can be used in which the field is divided into different sections and for each different sample the same matrix is used to select fields of view (e.g., the field can be divided into 9 sections, and from the center and the 4 corners, two HFOV are taken).</li>
	</ol>
	</li>
</ol>
5. Three-dimensional (3-D) Imaging of METs
NOTE: As METs are 3-D structures, by taking multiple z-stack images, which are reconstituted, may give valuable information.
<ol>
	<li>Section the lung specimens from paraffin blocks, at 200 &#181;m using a vibratome at an amplitude set at 1.8 mm and speed of 0.1-0.5 mm/s.</li>
	<li>Block lung tissue with 20% of the respective serum (10% fetal calf serum and 10% chicken serum) and then permeabilize in PBS supplemented and 3.75% Triton-X 100 for 7 h at room temperature under gentle agitation.</li>
	<li>Stain the sections for 16 h at 4 &#176;C with the relevant primary antibodies (MMP-9, H3Cit, and F4/80) in 200 &#181;L volumes in microcentrifuge tubes (antibody concentrations are listed in Table of Materials).</li>
	<li>Wash the sections in PBS, 3 times for 10 min before incubating with relevant secondary antibodies at room temperature for 1 h.</li>
	<li>Stain the lung sections for DAPI (1:5,000) in solution for 20 min, before adding the cover slips to the microscope slides in PBS.</li>
	<li>Obtain fluorescence images using an inverted confocal microscope (40x 1.3 NA) equipped with 405 nm, 440 nm, 473 nm, 543 nm, and 635 nm lasers.</li>
	<li>Record 3-D z-stacks of 0.54 &#181;m thickness with optimal z-sectioning for the 40x 1.3 NA oil objective. 
	NOTE: The software used will vary depending on the individual microscope. An example of how the software can be used for one microscope is provided in Supplementary File 1.</li>
</ol>
6. Image Analysis
NOTE: The analysis of samples requires the use of specific imaging analysis software and examples are listed in Table of Materials. While the analysis of results will depend on the specific program used, the listed points below are important.
<ol>
	<li>Analysis of BAL samples
	<ol>
		<li>Define the number of macrophages by selecting the blue channel for DAPI and assigning a minimum size for the cells (e.g., &#62; 18 &#181;m in diameter). Using the relevant software, measure the total number of macrophages per field.</li>
		<li>Count the number of cells that have the features of a MET by the presence of extracellular chromatin detected by DAPI with co-expression of other markers (e.g., MMP12, PAD2, and H3Cit). 
		NOTE: The number of markers that can be analyzed depends on the number of lasers available, but ideally in addition to DAPI, at least two other markers should be included. Other less specific parameters for MET expression (e.g., number of cells with extracellular chromatin and an enlarged nucleus) can be used.</li>
		<li>To compare the MET expression in BAL samples (between the control, smoke, and smoke/DNase treated groups), analyze a minimum of 100 BAL macrophages per sample.</li>
		<li>To measure secondary antibody and isotype control levels of fluorescence; measure a minimum of 100 cells in each sample for their fluorescence. Measure the average level of background fluorescence for each marker (e.g., H3Cit) using standard software.</li>
		<li>To define MET expression, count the cells with the typical phenotype (e.g., extracellular chromatin with co-expression of H3Cit and MMP9) and for each MET, measure the level of fluorescence of markers (e.g., H3Cit and MMP9). Exclude cells producing METs if their staining was not above background and isotype control.</li>
		<li>For human BAL samples, analyze a minimum of 100 cells for each sample for the percentage of macrophages that make METs. For murine samples, as the cells are smaller and METs are harder to define, analyze a larger number of cells for each sample (e.g., 200 macrophages).</li>
	</ol>
	</li>
	<li>Analysis of lung tissue samples
	<ol>
		<li>To determine the presence of METs in lung tissue, use specific macrophage marker such as F4/80.</li>
		<li>Define the presence of METs in lung tissue by using the co-localization of F4/80 in cells that express extracellular chromatin with other parameters as listed in section 6.1.</li>
		<li>Determine the levels of background fluorescence in samples with secondary antibody and the isotype controls. Exclude METs from analysis that are not above background.</li>
	</ol>
	</li>
</ol>

<ol>
	<li>Brinkmann, V., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neutrophil+extracellular+traps+kill+bacteria.">Neutrophil extracellular traps kill bacteria.</a> Science. 303 (5663), 1532-1535 (2004).</li><li>Brinkmann, V., Zychlinsky, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neutrophil+extracellular+traps:+is+immunity+the+second+function+of+chromatin?.">Neutrophil extracellular traps: is immunity the second function of chromatin?.</a> J Cell Biol. 198 (5), 773-783 (2012).</li><li>Jorch, S. 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D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inhibition+of+PAD4+activity+is+sufficient+to+disrupt+mouse+and+human+NET+formation.">Inhibition of PAD4 activity is sufficient to disrupt mouse and human NET formation.</a> Nat Chem Biol. 11 (3), 189-191 (2015).</li><li>Ruwanpura, S. M., McLeod, L., Dousha, L. F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Therapeutic+Targeting+of+the+IL-6+Trans-Signaling/Mechanistic+Target+of+Rapamycin+Complex+1+Axis+in+Pulmonary+Emphysema.">Therapeutic Targeting of the IL-6 Trans-Signaling/Mechanistic Target of Rapamycin Complex 1 Axis in Pulmonary Emphysema.</a> Am J Respir Crit Care Med. 194 (12), 1494-1505 (2016).</li><li>Brinkmann, V., Laube, B., Abu Abed, U., Goosmann, C., Zychlinsky, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neutrophil+extracellular+traps:+how+to+generate+and+visualize+them.">Neutrophil extracellular traps: how to generate and visualize them.</a> Journal of visualized experiments : JoVE. (36), (2010).</li><li>Chow, O. A., von Kockritz-Blickwede, M., Bright, A. 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The authors have no disclosures to make in relation to this work.

The method described in this review is based on that used for defining the presence of NETs14. Macrophages are by far the dominant cell type in BAL samples and this method of collection is particularly suited for studying METs. If red blood cells are present in the BAL, these cells should be lysed by using ammonium chloride. The BAL procedure will generally activate the macrophages and therefore it is expected that there will be METs present in un-stimulated samples. The BAL macrophages are usually very adherent. The BAL macrophages will generally not need a specific marker as these cells are the dominant cell type and can also be distinguished by their morphology. Usually in a BAL, greater than 80% of the cells are macrophages (and neutrophils are less than 5%), and after multiple washes, generally only the adherent leukocytes (i.e., the macrophages) remain6. If there is doubt about the ability to distinguish macrophages from neutrophils in humans, a neutrophil marker such as neutrophil elastase may be used. In lung tissue, a specific macrophage marker (e.g., F4/80) is required as macrophages are difficult to distinguish from other cell types. Macrophages have auto-fluorescence so the use of background and isotype controls is important; this is particularly the case with stimulated samples.
The best way to define the presence of METs remains to be determined. Specific pathways/processes, which are common to both neutrophils and macrophages are: (1) granular proteases, (2) citrullination of histones, and (3) PAD. PAD4 is more specific for neutrophils, whilst PAD2 is more prominent in monocytes/macrophages. The use of F4/80 is a well-accepted marker for murine macrophages, but human macrophages do not have such well-defined markers and this may pose issues when assessing human lung tissue for MET expression. Analyzing MET expression in lung tissue may be more difficult as there are many other cell types and the METs tend to be pushed onto the alveolar walls. When analyzing tissue sections, METs are best visualized when they are flat in cross-section; if the METs are in a different plane it may be difficult to determine if a MET is present. This issue can be addressed to some extent by making z-stacks to enable deeper tissue (3-D) planes for examining METs and the potential to visualize the METs in different aspects.
There is not a well-accepted method for defining the presence of METs in lung samples. The described methods are based on those used for visualizing NETs. Chow et al. described that the mitogen PMA induced METs in a macrophage cell line, as assessed by the presence of extracellular chromatin15. A subsequent study demonstrated that Mycobacterium tuberculosis induced METs in vitro, as defined by the presence of extracellular chromatin and H3Cit16. We have shown in vivo in a model of glomerulonephritis, that METs are present in the kidney as defined by co-localized chromatin, histone, and myeloperoxidase7. Finally, we have demonstrated the presence of METs in vitro in human lung macrophage by the combination of extracellular chromatin and MMP126. Our method can be used by other investigators to research this important facet of the inflammatory response.
It is likely that METs will be recognized to have a major role in chronic inflammatory disease. The processes that lead to NETosis are still not well-defined. The study of METs may provide significant insights into the mechanisms of trap formation. The development of protocols with more markers and functional studies of METs will further define the role of METs in disease.
There are critical steps that we have identified in this protocol. The human BAL samples are likely to have secondary bacterial contamination and the use of antibiotics in culture medium is important for limiting contamination. The primary and secondary antibodies can vary in their fluorescence, even with the same manufacturer. Finally, the analysis of lung tissue samples is more complex than BAL samples and requires time to develop a standardized approach.

Neutrophil extracellular traps (NETs), were first described by Brinkmann et al.1 They are predominantly produced in response to infection (especially to bacteria) and have an important role in host defense1,2. They have also been described to occur in response to non-infectious disease, including vasculitis and systemic lupus erythematosus (SLE); and to the mitogen phorbol 12-myrisate 13-acetate (PMA)2,3. It has recently been recognized that other cell types may also produce extracellular traps, including macrophages. Macrophage extracellular traps (METs) are not yet a well-defined entity in the literature4,5. We have recently established methods to detect the presence of METs both in vitro and in vivo6,7. In this article, the measurement of METs using confocal microscopy will be described.
Key features of NETosis which distinguish it from other cellular pathways (such as apoptosis8) are the extrusion of chromatin in conjunction with: (1) citrullination of histones (H3Cit)9, (2) co-expression of granule proteases10, and (3) involvement of peptidyl arginine deiminase (PAD) 411,12. Macrophages also express H3Cit, granule proteases, and PAD, and these features can be used to define the presence of METs.
METs may have a particularly important role in the lung, as the macrophage is the dominant cell present in the alveoli and airways of the lung and has the initial role in directing the cellular immune response to infection/inflammation. In addition, while much of the lung is empty space (e.g., within the alveoli), the METs are potentially able to expand into the space available, in contrast to solid organs.
The most widely used method to define the presence of NETs is by confocal microscopy. There is not yet a clearly defined way to measure METs. The technique for the measurement of NETs has been adapted to measure the presence of METs in this protocol. The main requirements for this method are access to confocal microscopy and appropriate imaging software for analysis.

<table><tbody><tr><td>&lt;strong&gt;Human samples: Primary antibodies&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Rabbit anti-human H3Cit (Citrulline R26)</td><td>Abcam</td><td>AB5103</td><td>10 ug/ml</td></tr><tr><td>Rabbit anti-human MMP12</td><td>Novus Biological</td><td>NB110-57214</td><td>1:100 concentration not quantifiable</td></tr><tr><td>Mouse anti-human MMP9</td><td>Novus Biological</td><td>AB119906</td><td>1:200 ascites, no concentration given</td></tr><tr><td>Rabbit anti-human PADI2/PAD2</td><td>Abcam</td><td>AB16478</td><td>7 ug/ml</td></tr><tr><td>Mouse anti-human PADI4/PAD4</td><td>Abcam</td><td>AB128086</td><td>10.1 ug/ml</td></tr><tr><td>Sheep anti-human NE</td><td>LifeSpan Bioscience</td><td>LS-B4244</td><td>25 ug/ml</td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Mouse samples: Primary antibodies&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Goat anti-mouse MMP9</td><td>Abcam</td><td>AF909</td><td>10 ug/ml</td></tr><tr><td>Rabbit anti-mouse H3Cit (Citrulline R26)</td><td>Abcam</td><td>AB5103</td><td>10 ug/ml</td></tr><tr><td>Rat anti-mouse F4/80</td><td>In-house (hybridoma)</td><td>In house</td><td>20 ug/ml</td></tr><tr><td>Sheep anti-human Anti-HNE /NE</td><td>Sapphire Bioscience</td><td>LS-B4244</td><td>25 ug/ml</td></tr><tr><td>Mouse anti-human &amp;shy;&amp;shy;&amp;shy;&amp;shy;PADI4/PAD4</td><td>Abcam</td><td>AB128086</td><td>10.1 ug/ml</td></tr><tr><td>Super-frost plus slides</td><td>Menzel</td><td>S41104A</td><td></td></tr><tr><td>Dapi-prolong gold</td><td>Molecular probes</td><td>P36931</td><td></td></tr><tr><td>Triton-X 100</td><td>Sigma-Aldrich</td><td>85111</td><td></td></tr><tr><td>Ammonium chloride</td><td>Sigma-Aldrich</td><td>E9434</td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Secondary antibodies&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Chicken anti-rabbit AF 488/</td><td>Life technologies</td><td>A-21441</td><td></td></tr><tr><td>Chicken anti-rabbit AF 594</td><td>Life technologies</td><td>A-21442</td><td></td></tr><tr><td>Chicken anti-goat AF 594</td><td>Life technologies</td><td>a-21468</td><td></td></tr><tr><td>Chicken anti-mouse AF488</td><td>Life technologies</td><td>A-21200</td><td></td></tr><tr><td>Donkey anti-sheep AF 594</td><td>Life technologies</td><td>A-11018</td><td></td></tr><tr><td>Chicken anti-mouse AF 647</td><td>Life technologies</td><td>A-21463</td><td></td></tr><tr><td>Donkey anti-sheep AF 594</td><td>Life technologies</td><td>A-11016</td><td></td></tr><tr><td>Isotype control</td><td></td><td></td><td></td></tr><tr><td>Rabbit IgG</td><td>In house</td><td></td><td></td></tr><tr><td>Rabbit IgG</td><td>In house</td><td></td><td></td></tr><tr><td>Mouse IgG1</td><td>BD Bioscience</td><td>550878</td><td></td></tr><tr><td>Rabbit IgG</td><td>In house</td><td></td><td></td></tr><tr><td>Mouse IgG2a</td><td>BioLegend</td><td>400201</td><td></td></tr><tr><td>Sheep IgG</td><td>In house</td><td></td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Software Programs&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Imaris</td><td>Bitplane</td><td></td><td></td></tr><tr><td>Image J</td><td>NIH</td><td></td><td></td></tr><tr><td>To average intensity of fluorphores a standard office application like Microsoft Excel can be used</td><td></td><td></td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Microscopes&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>C1 Confocal scanning microscope</td><td>Nikon</td><td></td><td></td></tr><tr><td>FV1200 Confocal scanning microscope</td><td>Olympus</td><td></td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Tissue sources&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Human BAL samples from the bronchoscopy suite at Monash Medical Centre</td><td></td><td></td><td></td></tr><tr><td>Mouse BAL samples and lung tissue from the Department of Pharmacology, University of Melbourne.</td><td></td><td></td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Media&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>RPMI</td><td>Sigma-Aldrich</td><td>r8758</td><td></td></tr><tr><td>Fetal calf serum</td><td>Sigma-Aldrich</td><td>F0926</td><td></td></tr><tr><td>L-glutamine</td><td>Sigma-Aldrich</td><td>G7513</td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Other reagents&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Sudan black</td><td>Sigma-Aldrich</td><td>199664</td><td></td></tr><tr><td>paraformaldehyde/periodate/lysine (PLP) fixative</td><td>Sigma-Aldrich</td><td>27387</td><td></td></tr><tr><td>Xylene</td><td>Sigma-Aldrich</td><td>214736</td><td></td></tr><tr><td>Ketamine</td><td>Sigma-Aldrich</td><td>K2753</td><td></td></tr><tr><td>Natural formalin</td><td>Sigma-Aldrich</td><td>42904</td><td></td></tr><tr><td>Paraffin</td><td>Sigma-Aldrich</td><td>327204</td><td></td></tr><tr><td>Agarose</td><td>Sigma-Aldrich</td><td>A2576</td><td></td></tr><tr><td>Solvent 3B</td><td>Hi-Chem</td><td>2026</td><td></td></tr><tr><td>Coverslips 12 ml</td><td>Sigma-Aldrich</td><td>S1815</td><td></td></tr><tr><td>Coverslips 60 x 24 ml</td><td>Sigma-Aldrich</td><td>C6875</td><td></td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Mice&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>c57 black 6</td><td>Monash animal research platform (MARP)</td><td></td><td></td></tr><tr><td>BALB/c</td><td>MARP</td><td></td><td></td></tr></tbody></table>

visualizing macrophage extracellular traps using confocal microscopy

A primary method used to define the presence of neutrophil extracellular traps (NETs) is confocal microscopy. We have modified established confocal microscopy methods to visualize macrophage extracellular traps (METs). These extracellular traps are defined by the presence of extracellular chromatin with co-expression of other components such as granule proteases, citrullinated histones, and peptidyl arginase deiminase (PAD). The expression of METs is generally measured after exposure to a stimulus and compared to un-stimulated samples. Samples are also included for background and isotype control. Cells are analyzed using well-defined image analysis software. Confocal microscopy may be used to define the presence of METs both in vitro and in vivo in lung tissue.

METs may be visualized from BAL samples, in lung tissue and in thicker lung sections with 3-D images. An example of METs visualized in a BAL sample is shown in Figure 1. The morphology of the METs will vary according to their stage of maturation. The first detectable feature on microscopy is the movement of the nucleus to the edge of the cell. This is followed by extracellular chromatin with other co-expressed mediators, such as H3Cit and granule proteases. In the earlier stages, the cell still has a roughly spherical shape with the extracellular trap expressed. At later stages, the MET formation is characterized by elongation of the body of the cell.
Lung tissue METs are shown in Figure 2. As the lungs are inflated with fluid to define the lung architecture, the METs will generally be pushed against the alveolar walls. The morphology of the METs will also vary depending on which plane the tissue was cut in. The standard sections used for lung tissue samples are 4-5 &#181;m in thickness. Thicker tissue sections enable multiple images to be taken and the METs can then be viewed in 3-D. The antibodies will only penetrate so far into the lung tissue and a section thickness of 25-50 &#181;m is optimal. An example of a 3-D image is shown in Figure 3 and in Video 1.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/56459/56459fig1.jpg" /> 
Figure 1: BAL METs. Human BAL METs formed after stimulation at different stages of development. METs were characterized by extracellular chromatin with co-expression of H3Cit and MMP9. Staining for (A) chromatin, (B) H3Cit, (C) MMP9, and (D) the merged image. Panel inserts are isotype controls. Scale bars = 10 &#181;m (15 &#181;m for isotype). An earlier stage MET is shown in the top right corner and has a roughly spherical shape. A more mature MET is shown in the middle of the field. Images were taken using a laser scanning confocal microscope and a 40x 1.0 NA oil objective. <a href="https://cloudflare.jove.com/files/ftp_upload/56459/56459fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/56459/56459fig2.jpg" /> 
Figure 2: Lung tissue METs. Murine METs in lung tissue after stimulation. The METs have been characterized by extracellular chromatin with co-expression of H3Cit, MMP9, and F4/80 (as a macrophage marker). Panel (A) shows a typical high-power field of view used to measure the number of METs; Panels (B-F) show the dashed square area under higher magnification. Staining for (B) chromatin, (C) H3Cit, (D) MMP9, (E) F4/80, and (F) the merged image. Insert panel is the isotype control. Scale bars = 20 &#181;m (20 &#181;m for isotype). METs are generally pushed against the alveolar walls. Images were taken using a laser scanning confocal microscope and a 40x 1.3 NA oil objective. <a href="https://cloudflare.jove.com/files/ftp_upload/56459/56459fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/56459/56459fig3.jpg" /> 
Figure 3: Three-dimensional view of lung section. Mouse lung tissue was fixed and cut into 25-35 &#181;m thick sections. Tissue was labeled with markers for METs and imaged with sections at 1 &#181;m thickness. Images were combined with a z-stack to create a 3-dimensional picture of a MET. Images were taken using a laser scanning confocal microscope and a 40x 1.3 NA oil objective. <a href="https://cloudflare.jove.com/files/ftp_upload/56459/56459fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Video 1" src="/files/ftp_upload/56459/56459video1.jpg" /> 
Video 1: Three-dimensional view of lung section. Video corresponds to samples presented in Figure 3. Axis ticks = 5 &#181;m. <a href="http://cloudflare.jove.com/files/ftp_upload/56459/Mets_1.avi" target="_blank">Please click here to view this video. (Right-click to download.)</a>

Watch this Scientific Journal Video about Visualizing Macrophage Extracellular Traps Using Confocal Microscopy at JoVE.com

Visualizing Macrophage Extracellular Traps Using Confocal Microscopy

Macrophage extracellular traps are a newly described entity. This article will concentrate on confocal microscopy methods and how they are visualized in vitro and in vivo from lung samples.

A primary method used to define the presence of neutrophil extracellular traps (NETs) is confocal microscopy. We have modified established confocal ...

visualizing-macrophage-extracellular-traps-using-confocal-microscopy

Nanyang Technological University

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Immunology and Infection

10.1K Views.  Monash Medical Centre. Macrophage extracellular traps are a newly described entity. This article will concentrate on confocal microscopy methods and how they are visualized in vitro and in vivo from lung samples.

Video: Visualizing Macrophage Extracellular Traps Using Confocal Microscopy

Neutrophil Extracellular Traps: How to Generate and Visualize Them

Neutrophil granulocytes are the most abundant group of leukocytes in the peripheral blood. As professional phagocytes, they engulf bacteria and kill them intracellularly when their antimicrobial granules fuse with the phagosome. We found that neutrophils have an additional way of killing microorganisms: upon activation, they release granule proteins and chromatin that together form extracellular fibers that bind pathogens. These novel structures, or Neutrophil Extracellular Traps (NETs), degrade virulence factors and kill bacteria1, fungi2 and parasites3. The structural backbone of NETs is DNA, and they are quickly degraded in the presence of DNases. Thus, bacteria expressing DNases are more virulent4. Using correlative microscopy combining TEM, SEM, immunofluorescence and live cell imaging techniques, we could show that upon stimulation, the nuclei of neutrophils lose their shape and the eu- and heterochromatin homogenize. Later, the nuclear envelope and the granule membranes disintegrate allowing the mixing of NET components. Finally, the NETs are released as the cell membrane breaks. This cell death program (NETosis) is distinct from apoptosis and necrosis and depends on the generation of Reactive Oxygen Species by NADPH oxidase5. 
Neutrophil extracellular traps are abundant at sites of acute inflammation. NETs appear to be a form of innate immune response that bind microorganisms, prevent them from spreading, and ensure a high local concentration of antimicrobial agents to degrade virulence factors and kill pathogens thus allowing neutrophils to fulfill their antimicrobial function even beyond their life span. There is increasing evidence, however, that NETs are also involved in diseases that range from auto-immune syndromes to infertility6.
We describe methods to isolate Neutrophil Granulocytes from peripheral human blood7 and stimulate them to form NETs. Also we include protocols to visualize the NETs in light and electron microscopy.

Neutrophil Extracellular Traps (NETs) are an important innate immune mechanism to fight pathogenic bacteria, fungi and parasites. Here we describe methods to isolate neutrophil granulocytes from human blood and to activate them to form NETs. We present preparation techniques to visualize NETs in light and electron microscopy.

Neutrophil granulocytes are the most abundant group of leukocytes in the peripheral blood. As professional phagocytes, they engulf bacteria and kill them ...

Use of an Optical Trap for Study of Host-Pathogen Interactions for Dynamic Live Cell Imaging

Dynamic live cell imaging allows direct visualization of real-time interactions between cells of the immune system1, 2; however, the lack of spatial and temporal control between the phagocytic cell and microbe has rendered focused observations into the initial interactions of host response to pathogens difficult. Historically, intercellular contact events such as phagocytosis3 have been imaged by mixing two cell types, and then continuously scanning the field-of-view to find serendipitous intercellular contacts at the appropriate stage of interaction. The stochastic nature of these events renders this process tedious, and it is difficult to observe early or fleeting events in cell-cell contact by this approach. This method requires finding cell pairs that are on the verge of contact, and observing them until they consummate their contact, or do not. To address these limitations, we use optical trapping as a non-invasive, non-destructive, but fast and effective method to position cells in culture.
Optical traps, or optical tweezers, are increasingly utilized in biological research to capture and physically manipulate cells and other micron-sized particles in three dimensions4. Radiation pressure was first observed and applied to optical tweezer systems in 19705, 6, and was first used to control biological specimens in 19877. Since then, optical tweezers have matured into a technology to probe a variety of biological phenomena8-13.
We describe a method14 that advances live cell imaging by integrating an optical trap with spinning disk confocal microscopy with temperature and humidity control to provide exquisite spatial and temporal control of pathogenic organisms in a physiological environment to facilitate interactions with host cells, as determined by the operator. Live, pathogenic organisms like Candida albicans and Aspergillus fumigatus, which can cause potentially lethal, invasive infections in immunocompromised individuals15, 16 (e.g. AIDS, chemotherapy, and organ transplantation patients), were optically trapped using non-destructive laser intensities and moved adjacent to macrophages, which can phagocytose the pathogen. High resolution, transmitted light and fluorescence-based movies established the ability to observe early events of phagocytosis in living cells. To demonstrate the broad applicability in immunology, primary T-cells were also trapped and manipulated to form synapses with anti-CD3 coated microspheres in vivo, and time-lapse imaging of synapse formation was also obtained. By providing a method to exert fine spatial control of live pathogens with respect to immune cells, cellular interactions can be captured by fluorescence microscopy with minimal perturbation to cells and can yield powerful insight into early responses of innate and adaptive immunity.

A method is described to individually select, manipulate, and image live pathogens using an optical trap coupled to a spinning disk microscope. The optical trap provides spatial and temporal control of organisms and places them adjacent to host cells. Fluorescence microscopy captures dynamic intercellular interactions with minimal perturbation to cells.

Dynamic live cell imaging allows direct visualization of real-time interactions between cells of the immune system1, 2; however, the lack of spatial and ...

In Vitro Stimulation and Visualization of Extracellular Trap Release in Differentiated Human Monocyte-derived Macrophages

The release of extracellular traps (ETs) by neutrophils has been identified as a contributing factor to the development of diseases related to chronic inflammation. Neutrophil ETs (NETs) consist of a mesh of DNA, histone proteins, and various granule proteins (i.e., myeloperoxidase, elastase, and cathepsin G). Other immune cells, including macrophages, can also produce ETs; however, to what extent this occurs in vivo and whether macrophage extracellular traps (METs) play a role in pathological mechanisms has not been examined in detail. To better understand the role of METs in inflammatory pathologies, a protocol was developed for visualizing MET release from primary human macrophages in vitro, which can also be exploited in immunofluorescence experiments. This allows further characterization of these structures and their comparison to ETs released from neutrophils. Human monocyte-derived macrophages (HMDM) produce METs upon exposure to different inflammatory stimuli following differentiation to the M1 pro-inflammatory phenotype. The release of METs can be visualized by microscopy using a green fluorescent nucleic acid stain that is impermeant to live cells (e.g., SYTOX green). Use of freshly isolated primary macrophages, such as HMDM, is advantageous in modeling in vivo inflammatory events that are relevant to potential clinical applications. This protocol can also be used to study MET release from human monocyte cell lines (e.g., THP-1) following differentiation into macrophages with phorbol myristate acetate or other macrophage cell lines (e.g., the murine macrophage-like J774A.1 cells).

Presented here is a protocol to detect macrophage extracellular trap (MET) production in live cell culture using microscopy and fluorescence staining. This protocol can be further extended to examine specific MET protein markers by immunofluorescence staining.

The release of extracellular traps (ETs) by neutrophils has been identified as a contributing factor to the development of diseases related to chronic ...

Morphological and Compositional Analysis of Neutrophil Extracellular Traps Induced by Microbial and Chemical Stimuli

Neutrophils function as the first line of cellular defense in an innate immune response by employing diverse mechanisms, such as the formation of neutrophil extracellular traps (NETs). This study analyzes the morphological and compositional changes in NETs induced by microbial and chemical stimuli using standardized in vitro methodologies for NET induction and characterization with human cells. The procedures described here allow the analysis of NET morphology (lytic or non-lytic) and composition (DNA-protein structures and enzymatic activity), and the effect of soluble factors or cellular contact on such characteristics. Additionally, the techniques described here could be modified to evaluate the effect of exogenous soluble factors or cellular contact on NET composition.
The applied techniques include the purification of polymorphonuclear cells from human peripheral blood using a double density gradient (1.079-1.098 g/mL), guaranteeing optimal purity and viability (&#8805; 95%) as demonstrated by Wright's staining, trypan blue exclusion, and flow cytometry, including FSC versus SSC analysis and 7AAD staining. NET formation is induced with microbial (Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans) and chemical (phorbol myristate acetate, HOCl) stimuli, and the NETs are characterized by DNA-DAPI staining, immunostaining for the antimicrobial peptide cathelicidin (LL37), and quantification of enzymatic activity (neutrophil elastase, cathepsin G, and myeloperoxidase). The images are acquired through fluorescence microscopy and analyzed with ImageJ.

Presented here is a protocol for the induction and analysis of in vitro neutrophil extracellular traps (NETs). Quantification of DNA, cathelicidin (LL37), and enzyme activity yielded data that show the variability in the composition and morphology of NETs induced by microbial and chemical stimuli under similar controlled conditions.

Neutrophils function as the first line of cellular defense in an innate immune response by employing diverse mechanisms, such as the formation of ...

Immunofluorescence Labelling of Human and Murine Neutrophil Extracellular Traps in Paraffin-Embedded Tissue

Neutrophil granulocytes, also called polymorphonuclear leukocytes (PMN) due to their lobulated nucleus, are the most abundant type of leukocytes. They mature in the bone marrow and are released into the peripheral blood, where they circulate for about 6&#8722;8 h; however, in tissue, they can survive for days. By diapedesis through the endothelium, they leave the blood stream, enter tissues, and migrate towards the site of an infection following chemotactic gradients.&#160;Neutrophils can combat invading microorganisms by phagocytosis,&#160;degranulation, and generation of neutrophil extracellular traps (NETs). This protocol will help to detect NETs in paraffin-embedded tissue. NETs are the result of a process called NETosis, which leads to the release of nuclear, granular, and cytoplasmic components either from living (vital NETosis) or dying (suicidal NETosis) neutrophils. In vitro, NETs form cloud-like structures, which occupy a space several times larger than that of the cells from which they descended. The backbone of NETs is chromatin, to which a selection of proteins and peptides originating from granules and cytoplasm are bound. Thereby, a high local concentration of toxic compounds is maintained so that NETs can capture and inactivate a variety of pathogens including bacteria, fungi, viruses, and parasites, while diffusion of the highly active NET components leading to damage in neighboring tissue is limited. Nevertheless, in recent years it has become apparent that NETs, if generated in abundance or cleared insufficiently, do have pathological potential ranging from autoimmune diseases to cancer. Thus, detection of NETs in tissue samples may have diagnostic significance, and the detection of NETs in diseased tissue can influence the treatment of patients. Since paraffin-embedded tissue samples are the standard specimen used for pathological analysis, it was sought to establish a protocol for fluorescent staining of NET components in paraffin-embedded tissue using commercially available antibodies.

Neutrophil extracellular traps (NETs) are three-dimensional structures generated by stimulated neutrophil granulocytes. It has become clear in recent years that NETs are involved in a wide variety of diseases. Detection of NETs in tissue may have diagnostic relevance, so standardized protocols for labelling NET components are required.

Neutrophil granulocytes, also called polymorphonuclear leukocytes (PMN) due to their lobulated nucleus, are the most abundant type of leukocytes. They ...

Medicine

Staining and Imaging to Visualize Neutrophil Extracellular Traps

Immunofluorescence Imaging of Neutrophil Extracellular Traps in Human and Mouse Tissues

Neutrophil extracellular traps (NETs) are released by neutrophils as a response to bacterial infection or traumatic tissue damage but also play a role in autoimmune diseases and sterile inflammation. They are web-like structures composed of double-stranded DNA filaments, histones, and antimicrobial proteins. Once released, NETs can trap and kill extracellular pathogens in blood and tissue. Furthermore, NETs participate in homeostatic regulation by stimulating platelet adhesion and coagulation. However, the dysregulated production of NETs has also been associated with various diseases, including sepsis or autoimmune disorders, which makes them a promising target for therapeutic intervention. Apart from electron microscopy, visualizing NETs using immunofluorescence imaging is currently one of the only known methods to demonstrate NET interactions in tissue. Therefore, various staining methods to visualize NETs have been utilized. In the literature, different staining protocols are described, and we identified four key components showing high variability between protocols: (1) the types of antibodies used, (2) the usage of autofluorescence-reducing agents, (3) antigen retrieval methods, and (4) permeabilization. Therefore, in vitro immunofluorescence staining protocols were systemically adapted and improved in this work to make them applicable for different species (mouse, human) and tissues (skin, intestine, lung, liver, heart, spinal disc). After fixation and paraffin-embedding, 3 &#181;m thick sections were mounted onto slides. These samples were stained with primary antibodies for myeloperoxidase (MPO), citrullinated histone H3 (H3cit), and neutrophil elastase (NE) according to a modified staining protocol. The slides were stained with secondary antibodies and examined using a widefield fluorescence microscope. The results were analyzed according to an evaluation sheet, and differences were recorded semi-quantitatively.
Here, we present an optimized NET staining protocol suitable for different tissues. We used a novel primary antibody to stain for H3cit and reduced non-specific staining with an autofluorescence-reducing agent. Furthermore, we demonstrated that NET staining requires a constant high temperature and careful handling of samples.

Author Spotlight: Neutrophil Extracellular Traps Imaging in Human and Mouse Tissues 

Neutrophil extracellular traps (NETs) are associated with various diseases, and immunofluorescence is often used for their visualization. However, there are various staining protocols, and, in many cases, only one type of tissue is examined. Here, we establish a generally applicable protocol for staining NETs in mouse and human tissue.

Neutrophil extracellular traps (NETs) are released by neutrophils as a response to bacterial infection or traumatic tissue damage but also play a role in ...

In Vitro Stimulation and Visualization of Macrophage Extracellular Traps

Source: Zhang, Y., et al. <a href="https://app.jove.com/v/60541">In Vitro Stimulation and Visualization of Extracellular Trap Release in Differentiated Human Monocyte-derived Macrophages.</a> J. Vis. Exp. (2019).
This video demonstrates in vitro stimulation of macrophage extracellular traps (METs) in human monocyte-derive macrophages using different inflammatory stimuli such as TNF-alpha, PMA, and HOCL. The video also demonstrates the method of SYTOX dye staining of METs for visualization.

1. Polarization of HMDM

	Under sterile conditions, prepare the M1 priming media by adding interferon &#947; (IFN&#947;; 20 ng/mL) and lipopolysaccharide ...

JoVE Encyclopedia of Experiments

Immunology

Immunodiagnostics

Imaging and Visualization Techniques

Characterization of Macrophage Extracellular Traps in Mouse Lung Tissue Samples

Source: Sharma, R., et al. <a href="https://app.jove.com/v/56459">Visualizing Macrophage Extracellular Traps Using Confocal Microscopy.</a> J. Vis. Exp. (2017)
In this video, we describe a protocol for the immunostaining and confocal microscopy-based visualization of macrophage extracellular traps (METs) in murine lung tissue. Tissue-resident macrophages are characterized by the expression of the macrophage-specific F4/80 surface glycoprotein marker, while METs are visualized by labeling the MET markers matrix metalloproteinase 9, citrullinated histone H3, and extracellular chromatin.

Source: Sharma, R., et al. Visualizing Macrophage Extracellular Traps Using Confocal Microscopy. J. Vis. Exp. (2017)
In this video, we describe a protocol ...

Immune Systems and Components

Assays and Functional Profiling

Visualization of Extracellular Traps in Macrophages from Human Bronchoalveolar Lavage Fluids

Source: Sharma, R. et al., <a href="https://app.jove.com/v/56459">Visualizing Macrophage Extracellular Traps Using Confocal Microscopy.</a> J. Vis. Exp. (2017)
This video demonstrates the immunolabeling of macrophage extracellular traps, METs, in bronchoalveolar macrophages from bronchoalveolar lavage fluid, and their visualization using a confocal microscope.

All procedures involving sample collection have been performed in accordance with the institute&#39;s IRB guidelines.
1. Bronchoalveolar Lavage (BAL) ...

Immunopathology

Assay and Analysis

Induction and Visualization of Neutrophil Extracellular Traps in Pre-Labeled Neutrophils

Source: Arends, E. J. et al., <a href="https://app.jove.com/v/59150">A High-throughput Assay to Assess and Quantify Neutrophil Extracellular Trap Formation.</a>&#160;J. Vis. Exp.&#160;(2019)
This video demonstrates the induction and visualization of neutrophil extracellular traps or NETs in pre-labeled neutrophils using patient serum containing anti-neutrophil cytoplasmic antibodies. Furthermore, using an impermeable DNA dye and fluorescence microscopy enables the visualization of NETs.

All procedures involving human participants have been performed in compliance with the institutional, national, and international guidelines for human ...