A subscription to JoVE is required to view this content. Sign in or start your free trial.
This protocol features a set of neutrophil functional assays to be used as a screening method to cover functions from different signaling pathways. The protocol includes an initial and simple evaluation of cell viability, purity, reactive oxygen species production, real-time migration, phagocytosis, and a preliminary suggestion of neutrophil extracellular traps.
Neutrophils are known as one of the first lines of defense in the innate immune response and can perform many particular cellular functions, such as chemotaxis, reverse migration, phagocytosis, degranulation of cytotoxic enzymes and metabolites, and release of DNA as neutrophil extracellular traps (NETs). Neutrophils not only have tightly regulated signaling themselves, but also participate in the regulation of other components of the immune system. As fresh neutrophils are terminally differentiated, short-lived, and highly variable among individuals, it is important to make the most of the collected samples. Researchers often need to perform screening assays to assess an overview of the many neutrophil functions that may be affected by specific conditions under evaluation. A set of tests following a single isolation process of normal density neutrophils was developed to address this need, seeking a balance between speed, comprehensiveness, cost, and accuracy. The results can be used to reason and guide in-depth follow-up studies. This procedure can be carried out in an average time of 4 h and includes the evaluation of cell viability, reactive oxygen species (ROS) production, real-time migration, and phagocytosis of yeast on glass slides, leaving enough cells for more detailed approaches like omics studies. Moreover, the procedure includes a way to easily observe a preliminary suggestion of NETs after fast panoptic staining observed by light microscopy, with a lack of specific markers, albeit enough to indicate if further efforts in that way would be worthwhile. The diversity of functions tested combines common points among tests, reducing the analysis time and expenses. The procedure was named NeutroFun Screen, and although having limitations, it balances the aforementioned factors. Furthermore, the aim of this work is not a definite test set, but rather a guideline that can easily be adjusted to each lab's resources and demands.
Neutrophils are the most abundant innate immune cells in human blood and are known to play a major part in infection and inflammation, being the first responders to arrive at the site of tissue damage1. In recent years, there has been a growing recognition of the crucial role that neutrophils play in a variety of diseases and in supporting homeostasis2. Neutrophils not only have tightly regulated signaling themselves, but also participate in the regulation of other components of the immune system3,4,5. Therefore, investigating n....
All experiments strictly followed the ethical guidelines set by the institutional review board at the University of Brasilia (process 13364819.0.0000.5558), and samples were identified by codes to ensure donor anonymity. The cells were obtained from normal healthy male donors aged 18-35 years, who signed the informed consent and met the following eligibility criteria: non-smokers/vapers, no chronic health conditions, and no history of inflammatory conditions in the last 14 days.
1. Blood.......
The density-based isolation method used in this study (Figure 1) met the criteria for the proposed experiments. Neutrophil parameters obtained from this method included viability ≥98%, purity ≥94%, and cell yield ≥1.5 x 107, with no activation detectable by the screening tests. Two relevant steps in the isolation of PMNs are anticoagulation and RBC removal. Keeping the anticoagulated blood tube or syringe at a gentle rocking before layering over the density .......
Neutrophils are highly dynamic and responsive cells that are short-lived and cannot yet be cryopreserved19, making investigations into their biology challenging. Therefore, it is essential to follow careful steps to obtain viable, enriched, and resting neutrophils11,20. This study employed a density-based isolation technique that emphasizes gentle and minimal manipulation, as well as the use of low temperatures until the activation step. A.......
The authors acknowledge the following funding agencies: FAPDF, CNPq, CAPES, UnB, FINEP, and FINATEC.
....Name | Company | Catalog Number | Comments |
CIM-Plate 16 | Agilent | 5665825001 | |
CLARIOstar Plate Reader | BMG LABTECH | US Patent Number 9,733,124 Product details: MARS Data Analysis Software | |
Dimethyl sulfoxide | Dinâmica | 1582 | |
DNAse I | Sigma - Aldrich | DN 25 | |
Ethylenediaminetetraacetic acid disodium salt dihydrate | Sigma - Aldrich | E5134 | |
Fast panoptic stain | Laborclin | 620529 | |
Glass slide | Exacta | 7102 | |
Hank’s Balanced Salt Solution with calcium, with magnesium, without phenol red. | Sigma - Aldrich | 55037C | |
Hank’s Balanced Salt Solution without calcium chloride, magnesium sulfate and sodium bicarbonate. | Sigma - Aldrich | H4641 | |
Heparin | Blau | 7896014655229 | |
Laminar flow cabinet | Veco | VLFS-12 | |
Microscope | Zeiss | 415501-0101-002 | Product details: Primostar 1 |
Mixing Block | BIOER | MB-102 | |
Neubauer improved bright-lined | New Optik | 1110000 | |
N-formyl-methionyl-leucyl-phenylalanine | Sigma - Aldrich | F3506 | |
Nitroblue tetrazolium | Neon | CAS 298-83-9 | |
Percoll | Cytiva | 17089101 | separation media |
Phorbol 12-myristate 13-acetate | Sigma - Aldrich | P8139 | |
Phosphate buffered saline tablet | Sigma - Aldrich | P4417 | |
ROTOFIX 32 A | Hettich | 1206 | |
Saccharomyces cerevisiae | Fleischmann | ||
Safranin | Sigma - Aldrich | 50240 | |
Sodium dodecyl sulfate | Cytiva | 17-1313-01 | |
Sonicator | Qsonica | Q125 | |
Trypan blue solution | Vetec | C.I. 23850 | |
Vortex Genie 2 | Scientific Industries, Inc. | 0K-0500-902 | |
xCELLigence Real-Time Cell Analysis (RTCA) DP (dual purpose) | Agilent | 380601050 | Product details: RTCA system composed of detection hardware, cell plates and software |
This article has been published
Video Coming Soon
ABOUT JoVE
Copyright © 2025 MyJoVE Corporation. All rights reserved