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5 protocols using rat anti mouse cd3 pe

1

Multicolor Flow Cytometry Immunophenotyping

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Splenocytes were stained with Mouse Anti-Mouse NK 1.1- APC (BD Biosciences, USA), Rat Anti-Mouse CD3-PE (BD Biosciences, USA), Rat Anti-Mouse CD4-PE (BD Biosciences, USA), and Rat Anti-Mouse CD8-APC (BD Biosciences) according to the manufacturer’s instructions. After staining, cells were analyzed by flow cytometry (Novocyte Flow Cytometer, ACEA Biosciences, USA). The positivity of CD8, CD4, and CD3 was determined by comparison with the defined cutoff values obtained with unstained control cells as previously described [18 (link)].
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2

Evaluating T Cell Proliferation in Mice

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T cell proliferation was assessed using a CellTrace CFSE Cell Proliferation Kit (ThermoFisher, USA). Briefly, the lymphocyte cells were isolated from spleen of C57BL/6 mouse, and then the cells were stained with CFSE (5 μM) staining solution diluted in DPBS for 20 min in a 37°C water bath. The CFSE-stained cells were added to RPMI1640 (Corning, USA) media with 10% heat-inactivated fetal bovine serum (FBS; Korea) and 100 U/ml penicillin and streptomycin (Gibco, USA) and then incubated for 5 min. Next, the cells were centrifuged at 300 ×g for 5 min, the supernatants were aspirated, and CFSE-stained cells were plated with a density of 1 × 107 cell per each well in a 6-well bottom plate and incubated for 5 days in 5% CO2 at 37°C. After 5 days, the cells were stained with Rat Anti-Mouse CD3-PE (BD Biosciences, NJ, USA), Rat Anti-Mouse CD4-PE (BD Biosciences, USA), and Rat Anti-Mouse CD8-APC (BD Biosciences). The stained cells were analyzed by flow cytometry (Novocyte Flow Cytometer, ACEA Biosciences, USA).
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Comprehensive Immune Profile Evaluation

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Whole blood was collected by retro-orbital bleeding into EDTA-coated tubes (Fisher Scientific). A complete blood cell count was acquired using a HemaVet950FS and specific lymphocyte subpopulations were assessed by FACS with cell specific markers for B-cells, T-cells, T-helper and T-suppressor cells at 17-weeks using the following antibodies (BD Biosciences): rat anti mouse CD3-PE; rat anti mouse CC45R/B220 PerCP; rat anti mouse CD8a antibody APC; rat anti mouse CD4 antibody Alexa 488. The percentages of cells in blood were determined on BD FACS Calibur (Becton Dickinson) and data were analyzed with FlowJo software (Tree Star, Inc.).
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4

Lymphocyte Subpopulation Analysis by Flow Cytometry

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Lymphocytes were labeled with APC Cy7 rat anti-mouse CD4 (Cat. No. 552051; BD Biosciences, San Diego, CA, USA), PE rat anti-mouse CD3 (555275; BD Biosciences, San Diego, CA, USA), and FITC rat anti-mouse CD25 (553071; BD Biosciences, San Diego, CA, USA) for 15 min at 4 °C. Then, the cells were washed with FACS buffer (PBS with 5% FBS) and fixed with 2% paraformaldehyde. Next, the lymphocytes were permeabilized with ice-cold methanol at room temperature (RT) for 20 min, washed, and labeled with Alexa Fluor rat anti-mouse Foxp3 (560401; BD Biosciences, San Diego, CA, USA). The cells were examined on a BD LSRFortessa cell analyzer (BD Biosciences, San Jose, CA, USA), and the obtained data were analyzed using BD FACSDIVA software version 7.0 (BD Bioscience, San Jose, CA, USA) [44 (link)].
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5

Multicolor Flow Cytometry Analysis of Murine T Cell Subsets

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Lymphocytes were suspended in 200 μL of FACS buffer (PBS with 5% FBS) in FACS tubes. To each tube, a mixture of monoclonal antibodies, including APC Cy7 rat anti-mouse CD4 (552051; BD Biosciences, San Diego, CA, USA), FITC rat anti-mouse CD25 (553071; BD Biosciences, San Diego, CA, USA), PE rat anti-mouse CD3 (555275; BD Biosciences, San Diego, CA, USA), and Alexa Fluor 700 rat anti-mouse CD8a (557959; BD Biosciences, San Diego, CA, USA), was added, and the cells were incubated at 4 °C for 15 min. Then, the cells were washed with FACS buffer and fixed with 2% paraformaldehyde. For intracellular staining, after washing, cells were permeabilized with ice-cold methanol at room temperature for 20 min. After washing, the cells were incubated at 4 °C for 20 min with Alexa Fluor 647 rat anti-mouse FoxP3 (560401; BD Biosciences, San Diego, CA, USA). After washing, the stained cells were analyzed on BD LSR Fortessa Cell Analyzer equipped with DIVA software. Cells were gated as follows: The lymphocyte population was gated on the FSC/SSC channel and was further gated for the CD3+ population, which was then further gated into CD4 and CD8 populations. From the CD3+CD4+ cells, the CD25+ population was taken as a parent for FoxP3 assignment. Each sample was prepared in triplicate, and 50,000 events were collected.
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