Basophil activation in unfractionated samples such as PBMC (note basophils are less dense than Ficoll) or whole blood can be measured by changes in the expression of cell surface markers or even intracellular events (e.g. phosphorylation, oxidative burst, calcium flux) by flow cytometry. Separate markers (e.g. as CD123+ HLA-DR-) are used to specifically identify basophils in addition to those used for assessment of activation.
This protocol is specifically for our collaboration with Aleena Banerji in Allergy Associates and Oncology.
- RPMI medium (cellgro, 10-040-CV; store at 4°C in dark)
- IL-3 (R&D) 2 μg/mL (stock aliquots are 10 μg/mL)
- 1 X FACS lysing solution (made from 10X stock with dH2O; store at 4°C; expires in 1 month)
- Staining Buffer (PBS + 2 mM EDTA + 0.5% BSA) (sterile filter, store at 4°C; aliquot in hood; expires in 2 months)
- monoclonal antibodies (e.g. CD63-FITC, CD203c-PE, CD123 PE-Cy5, HLA DR-PE-Cy7)
- stimulant aliquots (pre-made, 30 μL aliquots, distributed by Shreffler Lab; stored at -80°C)
- 5 mL round bottom polypropylene tubes (Falcon)
- 1.5 mL eppendorf tubes
- 15 and 50 mL conical tubes
- pipettes and tips
- serological pipettes (5, 10, 25)
- Platin drug (20X concentration)
- Obtain whole blood specimens collected in sodium heparin tube (green top). Keep at RT until use (within 16 hours).
- Remove pre-made stimulants (fMLP, Drug, Anti-IgE) from freezer and let thaw.
- Place 5 mL RPMI in water bath for ~5-10 minutes.
- Prepare 15 5 mL PP tubes for conditions (A-O):
- A: Unstained
- B: RPMI
- C: IL-3
- D: fMLP
- E: Anti-IgE
- F: Carboplatin 1 (1X)
- G: Carboplatin 2 (0.1X)
- H: Carboplatin 3 (0.01X)
- I: Carboplatin 4 (0.001X)
- J: Carboplatin 5 (0.0001X)
- K: Cisplatin 1 (1X)
- L: Cisplatin 2 (0.1X)
- M: Cisplatin 3 (0.01X)
- N: Cisplatin 4 (0.001X)
- O: Cisplatin 5 (0.0001X)
- Prepare RPMI w/IL-3 as follows:
- Add 4 μL of aliquot IL-3 (10 µL/mL) into 2.0 mL of warm RPMI in 5 mL PP tube. Mix well by inverting or vortex
- Except for "Unstained" and "RPMI" (tubes A and B), prepare all stimulants using RPMI IL-3
- For "A: Unstained" and "B: RPMI," use RPMI (no IL-3)
- For "C: IL-3," use RPMI IL-3 as is.
- For "D: fMLP," add 30 µL of 4 mM stock to 2370 µL RPMI IL-3 (1 part in 80), then add 20 µL of this dilution with 980 µL RPMI (1 part in 50) for final dilution.
- For "E: Anti-IgE," add 30 µL of 200 µL stock to 2670 µL RPMI IL-3 (1 part in 90).
- For "F: Carboplatin 1," add 30 µL of 20X carboplatin to 270 µL RPMI IL-3.
- For remainder of carboplatin series, take 30 µL from previous concentration in series and mix with 270 µL RPMI IL-3.
- For "K: Cisplatin 1," add 30 µL of 20X cisplatin to 270 µL RPMI IL-3.
- For remainder of cisplatin series, take 30 µL from previous concentration in series and mix with 270 µL RPMI IL-3.
- Transfer 250 µL of each stimulant into separate PP tubes, labeled A-O
- Gently mix blood by inverting green top tube.
- Transfer 250 μL of patient blood to each of the eleven PP tubes containing stimulants
- Incubate tubes for 20 minutes in 37°C incubator (5% CO2). Do not shake tubes!
- While incubating, prepare the antibody cocktail and store in 4°C refrigerator until you are ready to use it:
- To 900 uL staining buffer, add 90 μL each of:
- and 12 μL of:
- After the 20 minutes of incubation, remove the samples.
- Put samples on ice.
- Add 110 μL of antibody cocktail to tubes B -> K (DO NOT ADD TO A!).
- Gently mix cell suspension with mAb cocktail by flicking tube with finger or using #3 setting on vortex.
- Incubate for 20 min at 4°C. Protect from light.
- Add 2 mL staining buffer.
- Invert tubes 3X to mix
- Centrifuge for 5 minutes at 300g, RT
- Aspirate supernatant, taking care not to disturb cell pellet.
- Add 3 mL of 1x FACS lysing solution one tube at a time, recap and invert repeatedly until pellet is fully resuspended.
- Place tubes in the dark for 15 minutes or overnight in the refrigerator.
- Top off tube with staining buffer
- Centrifuge for 5 minutes at 800g, RT.
- Decant supernatant (do not double dump).
- Resuspend pellet in 50 μL staining buffer.
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- Who has experience with this protocol?
- Email Wayne Shreffler through OpenWetWare