Optimized Fibrin Gel Bead Assay for the Study of Angiogenesis
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PREPARING CELLS
- Bring up HUVEC and fibroblasts in M199/10% FBS/Pen-Strep (1:100) 1-2 days before beading.
- Switch medium to EGM-2 (Clonetics) the day before beading for HUVEC and the day before embedding for fibroblasts.
- A concentration of ~ 400 HUVEC per bead is needed.
- 20,000 fibroblasts per well is needed.
COATING THE BEADS WITH HUVEC - DAY -1
- Trypsinize HUVEC.
- Allow beads to settle (DO NOT CENTRIFUGE!). Aspirate the supernatant and wash the beads briefly in 1 mL of warm EGM-2 medium.
- Mix 2500 beads w/ 1X106 HUVEC in 1.5 mL of warm EGM-2 medium in a FACS tube. Place it vertically in the incubator. (This will be enough for ~10 wells. Scale up if needed)
- Incubate for 4 hours at 37°C, shaking the tube every 20 min. (Good coating is crucial for sprouting.)
- After 4 hours, transfer the coated beads to a T25 flask in 5mL of EGM-2 and leave O/N.
EMBEDDING COATED BEADS IN FIBRIN GEL - DAY 0
- Prepare the 2.0 mg/mL fibrinogen solution (See recipe section).
- Add 0.15 Units/mL of aprotinin to the fibrinogen solution.
- Transfer coated beads to a 15mL conical tube and let beads settle. Resuspend beads in 1mL of EGM-2 and transfer to a 1.5mL centrifuge tube.
- Wash the beads 3X with 1mL of EGM-2 by pipeting up and down SLOWLY.
- Count beads on a coverslip and resuspend in fibrinogen solution at a concentration of ~500 beads/mL.
- Add 0.625 Units/mL of thrombin to each well.
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Add 0.5 mL of the fibrinogen/bead suspension to each well of a 24-well plate.
Change the pipette tip for each well !!!
- Mix the thrombin and the fibrinogen by going up and down gently with the pipette tip ~ 4 to 5 times. Be careful not to make large bubbles.
- Leave the plate for 5 min in the hood, then place it in the 37°C-incubator for 10-15 min to generate a clot.
- While waiting for the clot, trypsinize fibroblasts.
- Add 1 mL of EGM-2 per well drop wise.
- Seed fibroblasts on top of fibrin gel at a concentration of 20,000 cells per well.
