Invasion Assay
 
Materials:
 
Falcon 24 well tissue
culture plate
Falcon Cell Culture Insert:
8μm pore size, 24 well format 
                                           Cat# 3097
Matrigel (Diluted in
DMEM/F12)
5% Glutaraldehyde in 1XPBS
0.5% Toluidine Blue in 2% Na2CO3
 
 Preparation
of Boyden Chamber:
 
 - Using sterile forceps remove cell wall inserts
     from their packaging and pit them into wells of a 24 wells plate.
- Wash inserts 2 times with 300μl DMEM/F12 
(Be
careful not to stab at the membrane)
    - Add 20μl of 1:6 diluted Matrigel (2-3 mg/ml 
      protein) to the center of each cell well inserts. Gently spread the Matrigel 
      across the entire surface of the membrane.
- Place coated inserts in incubator to allow the
     Matrigel to solidify for 20-30 min.
Preparation
of Cells for Assay:
 
 - Treat and grow cells according to experimental
     condition. It may be desirable to synchronize cells to the same growth
     state.
- Trypsinizing 
     and count of cells 
- Remove trypsin and resuspend with fresh medium.
- Plate 1X105 cells in 200 μl
     of defined medium into upper chamber.
- Add 300 μl of medium lower chamber.
- Culture for approximately 20 hours.
The
time varies for different cell lines and may be up to 48 hours for less
invasive cells.
 
Fixation
and Staining:
  
 - After culture, aspirate medium from lower
     chamber
- Add 0.5 ml of 5% Glutaraldehyde in 1XPBS,
     incubate for 10 min. @ R.T
- Aspirate Glutaraldehyde solution, wash each well
     3 times with D.W
- Add 0.5 ml 
     of 0.5 % Toluidine Blue staining solution into the lower chamber,
     incubate for 10-20 min @ R.T
- Aspirate solution from both upper and lower
     chamber, wash lower chamber 3 times with D.W
- Carefully wipe the inner surface of the upper
     chamber using a cotton swab. (Be careful not to press too firmly, the
     membrane may be popped out.) Invaded cells will be in the center of bottom
     of the membrane.
- Count the number of cells with q 20X objective
     of microscope. Count at least 3 fields per membrane.
 
Reference:
 
Andre Lochter, Anavella
Srebrow, Carolyn J. Sympson, Nathan Terracio, Zena Werb, and Mina J. Bissell
(1997)J. Biol. Chem., 272, 5007-5015