Induction of Epithelial-mesenchymal Transition in MDCK II Cells

Materials and Reagents

1. Sterile Cell Culture Dish, 100 × 20 mm (Sarstedt, catalog number: 83.3902 )

2. Serological pipettes: 5 ml (Sarstedt, catalog number: 86.1253.001 ), 10 ml (Sarstedt, catalog number: 86.1254.001 ), 50 ml (Sarstedt, catalog number: 86.1256.001 )

3. Tube 15 ml (Sarstedt, catalog number: 62.554.502 )

4. Tube 50 ml (Sarstedt, catalog number: 62.547.254 )

5. 1.5 ml microtubes (Sarstedt, catalog number: 72.690.301 )

6. Culture chambers: Lumox 8-well specimen slide detachable (Sarstedt, catalog number: 94.6150.801)

   Note: The procedure also works with Falcon^TM Chambered Cell Culture Slides, 8 wells, (Corning, catalog number: 354118).

7. Laboratory bottle, borosilicate 3.3 glass, 50 ml (VWR, catalog number: 215-3261 )

8. Laboratory bottle, borosilicate 3.3 glass, 1,000 ml (VWR, catalog number: 215-1595 )

9. Aluminium foil

10. ART^TM Barrier Specialty Pipette Tips: 10 µl (Thermo Scientific, catalog number: 2140 ), 200 µl (Thermo Scientific, catalog number: 2770 ), 1,000 µl (Thermo Scientific, catalog number: 2279 )

11. Microscope slide holder

12. Cover slips Menzel Glaser 24 × 60 mm (ThermoFisher Scientific, catalog number: E-4137 )

13. Parafilm

14. MDCK II cell line (Merck/Sigma-Aldrich, catalog number: ECACC 00062107 )

15. Eagle's Minimum Essential Medium (EMEM), 500 ml (ATCC, catalog number: 30-2003 )

16. Fetal bovine serum (FBS), 500 ml (Gibco, catalog number: 10270-106)

    Note: FBS does not require heat inactivation.

17. Dulbecco's phosphate-buffered saline (DPBS) 1×, no calcium, no magnesium, 500 ml (Gibco, catalog number: 14190-094 )

18. Trypsin-EDTA (0.25%), phenol red, 100 ml (Gibco, catalog number: 25200056 )

19. Recombinant Human HGF (HEK293 derived), 25 μg (Peprotech, catalog number: 100-39H )

20. Goat normal serum, 10 ml (Agrisera, catalog number: AS10 1548 )

21. Saponin, 10 g (Sigma-Aldrich, catalog number: S4521 )

22. Paraformaldehyde (PFA), 1 kg (Sigma-Aldrich, catalog number: 16005 )

23. Sodium chloride (NaCl), 1 kg (VWR Chemicals, catalog number: 27810.295 )

24. Potassium chloride (KCl), reagent grade, Reag. Ph Eur, 1 kg (Scharlau, catalog number: PO02001000 )

25. di-Sodium hydrogen phosphate dihydrate (Na₂HPO₄·2H₂O), 1 kg (Scharlau, catalog number: SO03391000 )

26. Potassium dihydrogen phosphate (KH₂PO₄), 1 kg (Merck, catalog number: 1048731000 )

27. VECTASHIELD^® Antifade Mounting Medium with DAPI, 10 ml (Vector Laboratories, catalog number: H-1200 )

28. Nail polish

29. Sodium hydroxide (NaOH), 1 kg (Merck, catalog number: 1064691000 )

30. Primary antibodies (Table 1)

    
    

    Table 1. Primary antibodies
    

    
    

31. Secondary antibodies (Table 2)

    
    

    Table 2. Secondary antibodies
    

    
    

32. Complete medium for MDCK II cells (see Recipes)

33. PBS 10× (see Recipes)

34. PBS 1× (see Recipes)

35. Blocking buffer (see Recipes)

36. Washing buffer (see Recipes)

37. 3% PFA (see Recipes)

38. 5% saponin (see Recipes)

Equipment

1. Counting chamber, type Burker (Hirschmann, catalog number: 8100201 )

2. Fume hood

3. Eppendorf^® Research^® plus pipette, 3-pack: 0.5-10 µl, 10-100 µl, 100-1,000 µl (Sigma-Aldrich, catalog number: Z683884 )

4. Integra Pipetboy 2 (VWR, catalog number: 612-0927 )

5. Heating and magnetic stirrer RH basic 2 (Dulova, catalog number: QSA337 )

6. Centrifuge VWR Compact Star CS4

7. 37 °C, 5% CO₂ cell culture incubator

8. Standard phase contrast microscope

9. Confocal microscope Zeiss 710

Software

1. ImageJ (https://imagej.nih.gov/ij/download.html)

Procedure

1. Starting MDCK II cell culture

   1. Prepare the complete medium for MDCK II cells (see Recipes).

   2. Thaw a vial with frozen MDCK II cells.

   3. Transfer the cells into a 15 ml Falcon tube containing the complete medium.

   4. Centrifuge the cells for 5 min at 1,500 rpm (214 × g).

   5. Discard the supernatant.

   6. Add 10 ml of complete medium. Pipette up and down.

   7. Transfer the cells into a cell culture dish.

   8. Culture cells at 37 °C, 5% CO₂ in cell culture incubator.

      
      

2. MDCK II cell passage

   1. Pre-warm complete medium and trypsin.

   2. Remove medium from the cells.

   3. Wash with 10 ml of DPBS.

   4. Add 2 ml of trypsin.

   5. Incubate cells for 5 min at 37 °C.

   6. Check under the microscope if cells are detached.

      Note: If cells are not detached, continue incubation for 2-5 min at 37 °C.

   7. Add 10 ml of complete medium.

   8. Pipette up and down.

   9. Transfer the cell suspension into a 15 ml tube.

   10. Centrifuge the cells for 5 min at 1,500 rpm (214 × g).

   11. Discard the supernatant.

   12. Seed the cells in a new cell culture dish. Use split ratio of 1:5.

   13. Culture cells at 37 °C.

       
       

3. Induction of EMT

   Day 0

   1. Seed 16,000 cells/well in an 8-well chamber slide.

      Note: For the induction of EMT in MDCK II cells, the cells were passaged less than 10 times.

   2. Incubate cells overnight.

      
      

   Day 1

   1. Prepare HGF stock 100 μg/ml and make aliquots:

      1. Spin down the vial with lyophilized HGF.

      2. Add 250 μl of sterile BSA 1 mg/ml (in PBS) to the vial with HGF.

      3. Mix by pipetting.

      4. Spin down.

      5. Make aliquots. Use sterile 1.5 ml tubes.

      6. Store the aliquots at -80 °C.

   2. Dilute the HGF stock with complete medium to final concentration 20 ng/ml. Mix by vortexing.

   3. Remove medium from the cells, that were seeded in the 8-well chamber slide.

   4. Add 0.5 ml of DPBS per well.

   5. Remove DPBS.

   6. Add complete medium containing HGF, use 0.5 ml medium per well.

      Note: For the control, treat cells with complete medium without HGF.

   7. Incubate the cells for 24 h at 37 °C.

      
      

4. Immunofluorescent staining and imaging

   Day 2

   1. Thaw:

      3% PFA (see Recipes)

      Goat serum

      5% saponin (see Recipes)

   2. Prepare:

      Washing Buffer (see Recipes)

      Blocking Buffer (see Recipes)

   3. Remove culture medium.

   4. Fix the cultures in 3% PFA for 10-15 min. Use 0.5 ml of PFA/well.

      Note: All immunostaining steps are performed at room temperature, except where otherwise provided.

   5. Wash the cultures with PBS 1× (see Recipes). Use 0.5 ml of PBS 1×/well.

   6. Add 0.5 ml of Blocking Buffer/well. Incubate for 1 h at room temperature.

   7. Incubate the cultures with primary antibodies (Table 1), overnight, at 4 °C. Cover the cultures with parafilm.

      1. Dilute anti-ZO-1 antibody at a ratio 1:200.

      2. Dilute anti-vimentin antibody at a ratio 1:500.

      3. Use Washing Buffer for dilution of antibodies.

      4. Use minimum 200 μl antibody solution/well.

         
         

   Day 3

   8. Remove antibody solution.

   9. Wash with PBS 1×. Use 0.5 ml of PBS 1×/well.

   10. Incubate the cultures with fluorescent secondary antibodies (Table 2) for 1 h.

       1. Dilute secondary antibodies at a ratio 1:500.

       2. Use Washing Buffer for dilution of antibodies.

       3. Use minimum 200 μl antibody solution/well.

       4. Cover the cultures with aluminium foil to protect from the light.

   11. Wash with PBS 1×. Use 0.5 ml of PBS 1x/well.

   12. Discard PBS 1×.

   13. Remove media chamber. Use removing device.

   14. Mounting

       1. Put few drops of mounting medium on a coverslip slide.

       2. Put the coverslip slide on the top of the slide containing the cultures. Avoid bubbles.

   15. Seal the mounted slide with nail polish.

   16. Store the slides in a microscope slide folder at 4 °C. Protect from light.

       
       

   Day 4

   Take images of the stained cells with a confocal microscope (Figure 1).

Data analysis

Confocal microscope images are analyzed with ImageJ software. In addition to phenotypical characterization by immunofluorescence, EMT-induced MDCK cells can be analyzed by western blotting, evaluation of cell roundness as well as measurement of the cell distance to the first and the second neighbor cell, as described by Farrell et al. (2014).

Figure 1. Phenotypical characterization of EMT in MDCK II cells. A. Experimental schedule: MDCK II cells were treated with hepatocyte growth factor (HGF) for 24 h, fixed and then stained for EMT markers. B. Immunostaining for vimentin and tight junction protein-1 (zonula occludens-1, ZO-1). DAPI was used for nuclear counterstaining. Objective 20×. Scale bar, 50 μm.

Notes

For successful and reproducible results, we recommend:

1. To strictly follow the manufacturer’s guidelines on HGF storage and to avoid repeated HGF freeze-thaw cycles.

2. That MDCK II cells should be weekly observed under the microscope to monitor the stability of phenotype.

3. That MDCK II cultures should never be overgrown (avoid > 80% confluency).

4. That cell culture media should be exchanged regularly (avoid acidic medium, that can be identified by color change from pink into yellow, as it can induce EMT).

Recipes

1. Complete medium for MDCK II cells

   450 ml Eagle's Minimum Essential Medium (EMEM)

   50 ml fetal bovine serum (FBS)

2. PBS 10×

   80 g NaCl

   2.2 g KCl

   14.2 g Na₂HPO₄·2H₂O

   2 g KH₂PO₄

   Adjust final volume to 1 L with distilled water

3. PBS 1×

   100 ml PBS 10×

   900 ml distilled water

4. Blocking buffer

   500 μl goat serum

   100 μl 5% saponin

   Adjust final volume to 10 ml with PBS 1×

   Store short-term at 4 °C

5. Washing buffer

   500 μl goat serum

   500 μl 5% saponin

   Adjust final volume to 50 ml with PBS 1×

   Store short-term at 4 °C

6. 3% PFA

   1.5 g PFA

   12.5 μl NaOH 6 M

   Adjust final volume to 50 ml with PBS 1×

   1. Combine all components in a glass bottle in a fume hood

   2. Add magnetic stirring bar

   3. Dissolve the PFA by stirring the solution on a magnetic stirrer at 56 °C in the fume hood

   4. Store aliquots at -20 °C

   5. Avoid freeze-thaw cycles

7. 5% saponin

   2.5 g saponin

   Adjust final volume to 50 ml with distilled water

   Make aliquots and store at -20 °C

Acknowledgments

The protocol was adapted from Farrell et al. (2014). This work was supported by the Swedish Cancer Society (Cancerfonden, CAN2017/735). We acknowledge the Biochemical Imaging Center at Umeå University. We thank Wai-Lok Yau for critical reading of the manuscript.

Competing interests

The authors declare no conflicts of interest.

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