Cell Cycle Analysis by DNA Content (Propidium Iodide)
Fixation:
1. Wash cells by centrifugation (e.g. 200 x g, 5 min, 4°C) in protein-free buffer, such as
Phosphate Buffered Saline without Ca+2 or Mg+2 (PBS).
2. (Optional) Repeat step 1.
3. Resuspend at 2 x 106 cells in 1 ml ICE COLD BUFFER. Cell number will effect
staining quality!
Optional: Use pre-coated or silanized polypropylene tubes to minimize sticking.
Pre-coat tubes overnight with 2% Bovine Serum Albumin (BSA) in PBS.
4. Vortex gently, slowly adding the cell suspension dropwise to 9 ml of 70% ethanol in a
15 ml polypropylene centrifuge tube (Falcon? Cat. No. [35]2097).
OR: Vortex gently, slowly adding the cell suspension dropwise to an equal volume of COLD ABSOLUTE ethanol.
Optional: Observe cell preparation with a microcope to verify minimum cell clumping.
5. Store at 4°C to - 40°C for AT LEAST 2 hours, 12 - 24 hours is best. Can be stored for
up to 2 years before staining.
6. Centrifuge cells at 200 x g, 10 min, 4°C.
7. Resuspend pellet in 3 ml COLD PBS and transfer to Falcon? 12 X 75 mm (Cat. No.
[35]2054) polystyrene tubes for staining if other tubes (polypropylene) were used for
the fixation steps above. Falcon? Cat. No. [35]2235 have nylon filter caps and will
remove clumps.
Staining with Propidium Iodide (PI)
1. Wash cells at least once with COLD PBS. Cells may form a diffuse ring-shaped pellet,
so centrifuge longer ( e.g. 200 x g, 10 min, 4°C).
2. Resuspend cells in 300 - 500 μl PI/Triton X-100 staining solution :
To 10 ml of 0. 1 % (v/v) Triton X-100 (Sigma) in PBS add 2 mg DNAse-free RNAse A (Sigma) and 0.40 ml of 500 μg/ml PI (e.g., Roche). Prepare freshly. A stock solution of PI, made by dissolving 1 mg PI in 2 ml water, can be stored several months at 0° to 4°C. (Or buy 500 μg/ml PI from Roche new Catalog # 11348639001, old Cat. No.
1348639)
Note: If the RNAse is not DNAse-free, boil a solution of 2 mg RNAse A in 1 ml
water for 5 min. Aliquot and store at -20°C.
3. Incubate 37°C for 15 minutes or for 30 min at 20°C.
4. Transfer tubes to ice or store at 4°C PROTECTED FROM LIGHT.
5. Acquire data on flow cytometer within 48 hours (but might last up to 2 weeks). May
require nylon mesh filtration (eg, Filcons, BD Cat. No. 340627) to remove cell clumps
or syringing (25 gauge, UCSD Storehouse # 7245) to break up cell clumps. Can
acquire 5-30 samples per hour, depending on cell preparation.
6. MulticycleAV (IBM-PC) or ModFit LT (Macintosh) is used to fit the data to various cell
cycle models. See below for examples
This a screen shot of a typical profile from MulticycleAV:
Click on this figure to see the full screen.
Here's a ModFit LT output example from the same FCS file:
Click on this figure to see the full screen.
References:
1. Shapiro, HM, Practical Flow Cytometry, second edition. New York: Alan R. Liss, Inc;
1988. 353 p.
2. Darzynkiewicz, Z, Nucleic Acid Analysis. In: Robinson, JP, managing editor. Current
Protocols in Cytometry. New York : J Wiley & Sons, Inc; 1997. Chapter 7.