PBMC isolation
Michael Morgan
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Abstract
Isolation of PBMCs from fresh whole human blood in Lithium Heparin blood tubes.
Steps
Lymphocyte separation
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Start with everything at room temperature:
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Add 15 mL Ficoll-Paque Plus to each SepMate tube by pipetting directly into centre of plastic separator (try not to introduce a lot of air beneath the separator)
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Pool anti-coagulated blood tubes (3 x 9 mL Li Hep tubes) – should come to 27ml
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Dilute 1:1 in PBS + 2% FBS (now have ~54 mL diluted blood)
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Layer blood on top of Ficoll-Paque Plus by gently pipetting down the side of the SepMate tube (avoid pipetting directly above the small notches as this lets blood through to below the separator)
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Cap tightly and spin at 1200 x g, 10m, RT, accelerator and break on full
Washing
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Cool PBS + 2% FBS in refrigerator and set centrifuge to cool (4C, though 10C should be sufficient)
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Pour interface off SepMate tube into new 50 mL falcon (2 SepMate tubes per falcon – if odd number of tubes, even out the volumes between falcons)
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Top cells up to 45 mL with chilled PBS + 2% FBS, mix well
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Centrifuge 900 x g, 10m in cooled centrifuge
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Meanwhile, centrifuge 5 mL serum tube in the same spin
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Discard supernatant and flick to dislodge pellet
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Resuspend cells in chilled PBS + 2% FBS and pool cells from each individual into 1 tube with 40 mL buffer
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Centrifuge 300 x g, 10m in cooled centrifuge
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Meanwhile, aliquot serum (avoid any red) and store aliquots in freezer (these do not contain any human cells)
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Discard supernatant and flick to dislodge pellet
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Resuspend cells in 25 mL chilled PBS + 2% FBS
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Take 10 uL aliquot and count on haemocytometer
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Centrifuge 300 x g, 10m in cooled centrifuge
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Discard supernatant and pipet off final drips, flick to dislodge pellet
Freezing
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Resuspend cells in chilled 1-1.5 mL FBS + 10% DMSO (if more than 15 million cells, make multiple aliquots) – Freeze in ~5million cell aliquots
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Rapidly move cryovials to Mr Frosty and put in -80C Freezer