PBMC isolation

Michael Morgan

Published: 2022-03-09 DOI: 10.17504/protocols.io.b539q8r6

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Abstract

Isolation of PBMCs from fresh whole human blood in Lithium Heparin blood tubes.

Steps

Lymphocyte separation

1.
  •   Start with everything at room temperature:
    
2.
  •   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)
    
3.
  •   Pool anti-coagulated blood tubes (3 x 9 mL Li Hep tubes) – should come to 27ml
    
4.
  •   Dilute 1:1 in PBS + 2% FBS (now have ~54 mL diluted blood)
    
5.
  •   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)
    
6.
  •   Cap tightly and spin at 1200 x g, 10m, RT, accelerator and break on full 
    

Washing

7.
  •   Cool PBS + 2% FBS in refrigerator and set centrifuge to cool (4C, though 10C should be sufficient)
    
8.
  •   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)
    
9.
  •   Top cells up to 45 mL with chilled PBS + 2% FBS, mix well
    
10.
  •   Centrifuge 900 x g, 10m in cooled centrifuge
    
11.
  •   Meanwhile, centrifuge 5 mL serum tube in the same spin
    
12.
  •   Discard supernatant and flick to dislodge pellet
    
13.
  •   Resuspend cells in chilled PBS + 2% FBS and pool cells from each individual into 1 tube with 40 mL buffer
    
14.
  •   Centrifuge 300 x g, 10m in cooled centrifuge
    
15.
  •   Meanwhile, aliquot serum (avoid any red) and store aliquots in freezer (these do not contain any human cells)
    
16.
  •   Discard supernatant and flick to dislodge pellet
    
17.
  •   Resuspend cells in 25 mL chilled PBS + 2% FBS
    
18.
  •   Take 10 uL aliquot and count on haemocytometer
    
19.
  •   Centrifuge 300 x g, 10m in cooled centrifuge
    
20.
  •   Discard supernatant and pipet off final drips, flick to dislodge pellet  
    

Freezing

21.
  •   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
    
22.
  •   Rapidly move cryovials to Mr Frosty and put in -80C Freezer         
    

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