Materials and Reagents

10 cm plate (TPP Techno Plastic Products, catalog number: 93100 )
6-well plate (TPP Techno Plastic Products, catalog number: 92006 )
10 ml pipettes (Bioswisstec, catalog number: 515210 )
5 ml pipettes (Bioswisstec, catalog number: 515205 )
15 ml Falcon tube (Greiner Bio One International, catalog number: 188271 )
Glass Pasteur pipette (HUBERLAB, catalog number: 1.1127.01 )
Mouse embryonic stem cells (E14TG2a mESC line obtained from ATCC: ES-E14TG2a) (ATCC, catalog number: CRL-1821 )
Phosphate-buffered saline (PBS) 1x (Thermo Fisher Scientific, Gibco^TM, catalog number: 10010015 )
Trypsin-EDTA 0.05% (Thermo Fisher Scientific, Gibco^TM, catalog number: 25300054 )
Alkaline phosphatase Kit (Sigma-Aldrich, catalog number: 86R-1KT )
ddH₂O (Sigma-Aldrich, catalog number: 99053 )
Note: This product has been discontinued.
Gelatin (Sigma-Aldrich, catalog number: G1890 )
Dulbecco’s modified Eagle medium (DMEM) high glucose (Sigma-Aldrich, catalog number: D6429 )
Fetal bovine serum (FBS) (Thermo Fisher Scientific, Gibco^TM, catalog number: 10270106 )
Leukemia inhibitory factor (LIF) 10 millions unit/ml (Merck, catalog number: ESG1107 )
2-Mercaptoethanol (βM) 50 mM (Thermo Fisher Scientific, Gibco^TM, catalog number: 31350010 )
Mixture of penicillin and streptomycin (PS) (Sigma-Aldrich, catalog number: P0781 )
N2B27 (Takara Bio, catalog number: Y40002 )
MAPK/ERK inhibitor 0.4 μM (PD03) (Stemolecule PD0325901) (STEMCELL Technologies, catalog number: 72184 )
GSK3β inhibitor 3 μM (Chiron) (Stemolecule CHIR99021) (STEMCELL Technologies, catalog number: 72054 )
Acetone (Merck, catalog number: 1.00014.1000 )
Formaldehyde 37% (Sigma-Aldrich, catalog number: 47608-1L-F )
0.2% gelatin solution (see Recipes)
MES medium (see Recipes)
MEF medium (see Recipes)
2i + LIF medium (see Recipes)
Fixative solution (see Recipes)
Substrate solution (see Recipes)

Equipment

Heracall^TM 150i incubator (37 °C and 8% CO₂) (Thermo Fischer Scientific, Thermo Scientific^TM, model: Heracall^TM 150i )
Centrifuge (Eppendorf, model: 5810 )
Tissue culture hood (FASTER, model: Safe FAST Premium 209, catalog number: F00024900000 )
Millipore Scepter^TM 2.0 cell counter (EMD Millipore, model: Scepter^TM 2.0, catalog number: PHCC00000 ) (or any cell counter)
Inverted microscope (Nikon Instruments, model: Eclipse TS100 )

Software

ImageJ software 1.48v
Adobe Photoshop CS6
GraphPad Prism 6.0a software

Procedure

Maintenance of mESCs
1. mESCs are routinely cultured on 10 cm dish pre-coated with 0.2% gelatin (see Recipes) in 10 ml of MES medium (see Recipes), in an 8% CO₂ incubator at 37 °C (Figure1A).
2. Medium is changed every other day.
  Note: Special attention should be taken to avoid confluency (> 70%) of mESCs (Figure 1B) in maintenance cultures as it might result in detrimental differentiation of the cells.
  
  Figure 1. Typical morphologies of mESCs. Feeder-free undifferentiated mESCs are shown at low 20-30% (A) and high 60-70% (B) density. Healthy, emergent mESCs grow as tightly formed, refractile colonies throughout passages (A). Over confluency (> 70%) of mESCs (B) creates flat colony morphology and potential differentiation.
Exit from pluripotency assay
1. Coat a 6-well plate with 0.2% gelatin (500 μl per well) and verify that the gelatin is well distributed. Place the plate in the incubator.
2. Remove the media from a 50% confluent mESCs 10 cm dish. Wash once with 4 ml of 1x PBS. Add 2 ml of trypsin-EDTA to the cells and verify that the trypsin is well distributed. Place the cells back in the incubator for 5 min. Verify under the microscope that the mESC colonies are detached from the dish.
3. Add 4 ml of MEF media (see Recipes) to the dish to inactivate the trypsin. Use a 5 ml pipette gently up and down to achieve single cells and move them in a 15 ml Falcon tube.
  Note: Try to achieve a single cell suspension and be careful to avoid too many bubbles.
4. Count the cell density using a cell counter or equivalent method.
5. Centrifuge 2 x 10⁴ cells in a new tube at 190 x g for 5 min.
  Note: All centrifugations are carried at room temperature.
6. Carefully resuspend the cell pellet using 2 ml of 2i + LIF media (see Recipes).
7. Plate the 2 x 10⁴ mESCs in 2 ml of 2i + LIF medium in the 6-well pre-coated plate with 0.2% gelatin. Medium is changed every other day.
  Notes:
  1. Do not forget to remove the gelatin before plating the cells.
  2. The day on which the culture is started is designated as Day 0.
8. After 3 days, aspirate the 2i + LIF media without perturbing the mESC colonies (Day 3) and add N2B27 media (without LIF nor inhibitors) for 4 days (permissive media). Medium is changed every other day.
9. At Day 7, remove the N2B27 (permissive media) media without perturbing the mESC colonies and reintroduce 2i + LIF media for 3 additional days. Medium is changed every other day.
10. On Day 10 alkaline phosphatase staining can be performed (Figure 2).
  
  Figure 2. Alkaline phosphatase (AP) staining after exit from pluripotency assay. A. Whole 6-well after AP staining of wildtype mESCs; B. Wildtype mESCs are colorless and/or differentiated; C. Whole 6-well after AP staining of Dgcr8_KO mESCs; D. Dgcr8_KO mESCs cannot exit pluripotency and appear purple and undifferentiated; E. Number of positive clonal AP staining of cells after exit from pluripotency assay.
Alkaline phosphatase staining
1. Aspirate the 2i medium with a Pasteur pipette.
2. Wash once the cells with 1 ml of 1x PBS per well.
  Note: Be careful not to wash off the colonies from the plate.
3. Fix the cells carefully for 45 sec with 0.5 ml fixative solution (see Recipes).
  Note: Prolonged fixation can destroy alkaline phosphatase activity.
4. Wash the cells twice with 0.5 ml ddH₂O.
  Note: Be careful not to wash out the colonies from the plate.
5. Add 0.5 ml substrate solution (see Recipes) for 15 min at room temperature in the dark (either drawer or aluminum foil).
6. Wash with 0.5 ml ddH₂O.
7. Let the plate air dry overnight in a drawer.
Clonal alkaline phosphatase positive number quantification
1. Entire 6-well plates used for alkaline phosphatase staining are scanned with a printer/scanner machine to capture the total plate area in a single image (Figures 2A and 2C). More detailed images are also acquired with the microscope to better observe the morphology and alkaline phosphatase staining intensity in the different cell lines (Figures 2B and 2D).
2. Scanned PDF images are converted into TIFF images with Adobe Photoshop CS6.
3. Images are processed using ImageJ software 1.48v as follows:
  1. Number of alkaline phosphatase positive colonies is calculated on threshold intensity of inverted regions that are user–selected (full well–identical areas between conditions)
  2. Using the Analyze Particles tool (default parameters, ImageJ) the total number of alkaline phosphatase colonies is counted.
  3. Total number of alkaline phosphatase positive colonies is depicted in a graph as a clonal assay (Figure 2E).

Data analysis

Number of clonal AP positive colonies is expressed as ± SEM. Statistical differences can be measured by Student’s t-test. A value of P < 0.05 is considered significant. Data analysis can be performed using GraphPad Prism 6.0a software. AP staining must be performed in triplicate. The original research papers containing the aforementioned protocol are Cirera-Salinas et al., 2017 and Bodak et al., 2017.

Notes

The aforementioned protocol has been designed for RNAi mutant mESCs with strong proliferative defects. If other mouse ESC lines are used, we recommend to first adapting the cell lines to the 2i media. The adaption time varies from 3 days for good adherent cell lines, to 5-7 days if the cells have difficulties to attach to the plate. If the mESC line did not attach well, treat the plate with 0.2% gelatin for 24 h in the incubator before to plate them. Morphology of the cells is a good indicative for the adaptation as the cells become very round when adapted to the 2i media. Usually mESCs need 2 days in permissive media to exit from pluripotency. Finally, independently of the cell line used, 3 days in 2i media are necessary before staining with alkaline phosphatase.

Recipes

0.2% gelatin
Dilute 1 g of gelatin from porcine skin with 500 ml of ddH₂O, mix well and then autoclave solution
MES medium
MEF medium
2i + LIF medium
Fixative solution (15 ml)
12.25 ml acetone
3.92 ml citrate (provided 25 mM solution from the Sigma-Aldrich kit)
1.5 ml 37% formaldehyde
Substrate solution (3 ml)
2.81 ml ddH₂O
62.5 µl nitrite (provided by the Sigma-Aldrich kit)
62.5 µl FRV (provided by the Sigma-Aldrich kit)
62.5 µl of Naphthol (provided by the Sigma-Aldrich kit)
Note: The order of the substrates nitrite (1st), FRV (2nd) and Naphthol (3^rd) is important. Liquid has to be yellow before adding it to the cells.

Acknowledgments

This protocol was originally published as part of Cirera-Salinas et al. (2017). The authors wish to thank M. Bodak for fruitful discussions. D. C-S is supported by a Post-doctoral fellowship from the Peter and Traudl Foundation.

References

Betschinger, J., Nichols, J., Dietmann, S., Corrin, P. D., Paddison, P. J. and Smith, A. (2013). Exit from pluripotency is gated by intracellular redistribution of the bHLH transcription factor Tfe3. Cell 153(2): 335-347.
Bodak, M., Cirera-Salinas, D., Yu, J., Ngondo, R. P. and Ciaudo, C. (2017). Dicer, a new regulator of pluripotency exit and LINE-1 elements in mouse embryonic stem cells. FEBS Open Bio 7(2): 204-220.
Cirera-Salinas, D., Yu, J., Bodak, M., Ngondo, R. P., Herbert, K. M. and Ciaudo C. (2017). Non-canonical function of DGCR8 controls mESCs exit from pluripotency. J Cell Biol.
Ying, Q. L., Stavridis, M., Griffiths, D., Li, M. and Smith, A. (2003). Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture. Nat Biotechnol 21(2): 183-186.
Ying, Q. L., Wray, W., Nichols, J., Battle-Morera, L., Doble, B., Woodgett, J., Cohen, P. and Smith, A. (2008). The ground state of embryonic stem cell self-renewal. Nature 453(7194): 519-23.