Phosphoproteomic Analysis and Organotypic Cultures for the Study of Signaling Pathways

Materials and reagents

Biological materials

For organotypic tissue culture

1. MRC-5 (ATCC, catalog number: CCL-171)

2. N/TERT-1 (James G. Rheinwald, Harvard Institute of Medicine)

   
   

For proteomics

1. Amine (NH2) functional microparticles, MagReSyn^® Amine [ReSyn Biosciences (Pty) Ltd., South Africa]

2. Hydroxyl terminated beads, MagReSyn^® Hydroxyl [ReSyn Biosciences (Pty) Ltd., South Africa]

3. Magnetic microparticles with chelated Ti4 + metal ions for highly specific phosphopeptide enrichment, MagReSyn^® Ti-IMAC HP [ReSyn Biosciences (Pty) Ltd., South Africa]

   
   

Reagents

For organotypic tissue culture

1. Penicillin/streptomycin (Thermo Fisher, Gibco, catalog number: 151401)

2. DMEM (Thermo Fisher, Gibco, catalog number: 41966029)

3. Keratinocyte-SFM (Thermo Fisher, Gibco, catalog number: 17005034)

4. TrypLE (Thermo Fisher, Gibco, catalog number: 12605028)

5. Bovine pituitary extract (BPE) (Thermo Fisher, Gibco, catalog number: 13028014)

6. Fetal calf serum (FCS) (HyClone, catalog number: SH30071.03HI)

7. EGF (Thermo Fisher, Gibco, catalog number: PHG0314)

8. Insulin (Sigma-Aldrich, catalog number: 11070-73-8)

9. Hydrocortisone (Sigma-Aldrich, catalog number: H0888)

10. Triiodothyronine (T3) (Sigma-Aldrich, catalog number: T2752)

11. L-Glutamine (Thermo Fisher, Gibco, catalog number: A2916801)

12. Hams F12 (Thermo Fisher, Gibco, catalog number: 11765-054)

13. Rat tail collagen I (made in own lab [12])

14. Adenine (Sigma-Aldrich, catalog number: A8626)

15. Hydrochloric acid (HCl) (Sigma-Aldrich, catalog number: H1758)

16. Dulbecco’s phosphate buffered saline (PBS) (Sigma-Aldrich, catalog number: D5652)

17. Bovine serum albumin (BSA) (Sigma-Aldrich, catalog number: A7979)

18. Sodium hydroxide (NaOH) (Sigma-Aldrich, catalog number: 655104)

19. Calcium chloride (CaCl₂·2H₂O) (Sigma-Aldrich, catalog number: C7902)

20. Gentamycin sulphate (Sigma-Aldrich, catalog number: G1264)

21. Cholera enterotoxin (Sigma-Aldrich, catalog number: C8180)

22. 10× minimum essential media (10× MEM) (Thermo Fisher, Gibco, catalog number: 11430-030)

23. Sodium bicarbonate (Thermo Fisher, Gibco, catalog number: 15750037)

24. Tissue-Tek^® (SAKURA, catalog number: 4583)

25. Formalin solution neutral buffered, 10% (Sigma-Aldrich, catalog number: HT501128)

26. Sucrose (Sigma-Aldrich, catalog number: S0389)

27. Isopentane (Sigma-Aldrich, catalog number: PHR1661)

    
    

For proteomics

1. Lysis buffer, composed of 2% sodium dodecyl sulfate (SDS), 5 mM tris(2-carboxyethyl)phosphine (TCEP), 5.5 mM chloroacetamide (CAA), and 100 mM Tris pH 8.5; used for cell lysis

2. Acetonitrile (ACN), LC grade (Supelco^TM Analytical, catalog number: 75-05-8), used in various concentrations throughout the protocol, namely 70% for dilution of lysates, 95% for washing proteins, and 40% and 60% for elution on SepPak. ACN is also used for TMT-labeling

3. Ethanol (anhydrous) (Sigma-Aldrich, catalog number: 459836), used in 70% concentration for washing proteins after aggregation

4. 50 mM ammonium bicarbonate (ABC) (Sigma-Aldrich, catalog number: 09830), used for protein digestion and for resuspending TMT-labeled peptides

5. 50% trifluoroacetic acid (TFA), HPLC (Supelco^TM Analytical, catalog number: TX1276), used for acidification of samples post digestion

6. 1 M TEAB, pH 8 (Thermo Scientific^TM, catalog number: 90114), used to achieve a final concentration of 100 mM in TMT-labeling

7. 50% hydroxylamine (Thermo Scientific^TM, catalog number: 90115), used to quench the TMT-labeling reaction

8. 0.1% formic acid (v/v) in water (LC–MS grade) (Thermo Scientific^TM, catalog number: 85170), used for resuspension of each TMT-labeled sample before pooling

9. Loading buffer, composed of 80% ACN, 5% TFA, and 1 M glycolic acid (Sigma-Aldrich, catalog number: 8.04104); used for resuspending peptides for phosphopeptide enrichment

10. 1% ammonia (ammonia solution 25%) (Supelco, catalog number: 105428), used for elution of phosphopeptides

11. 5 mM ABC (buffer A) and 100% ACN (buffer B), used in high pH reversed-phase peptide fractionation

12. Pierce^TM BCA Protein Assay kit (Thermo Scientific^TM, catalog number: 23225)

13. TMTpro^TM 16plex label reagent set (Thermo Scientific^TM, catalog number: A44520)

14. LysC, Lysyl endopeptidase (Fujifilm Wako, catalog number: 129-02541)

15. Trypsin, Sequencing grade modified trypsin (Promega, catalog number: V511X)

16. Sep-Pak C18 1 cc Vac Cartridge (Waters, catalog number: WAT054955)

17. Acquity CSH C18 1.7 μm, 1 mm × 150 mm column (Waters, catalog number: 186006935)

    
    

Solutions

1. Adenine (see Recipes)

2. Cholera enterotoxin (CT) (see Recipes)

3. Hydrocortisone (HC) (see Recipes)

4. Epidermal growth factor (EGF) (see Recipes)

5. Triiodothyronine (T3) (see Recipes)

6. Calcium chloride (CaCl₂) (see Recipes)

7. Insulin (1,000× for 5 µg/mL) (see Recipes)

8. Sodium bicarbonate (71.2 mg/mL milli q water) (see Recipes)

9. Keratinocyte serum free medium (K-SFM) complete (see Recipes)

10. Organotypic culture medium (see Recipes)

11. DMEM 10% FBS (DMEM-10) (see Recipes)

    
    

Recipes

For organotypic tissue culture

1. Adenine

   Prepare 2.4 mg/mL of adenine in HCl (this is a 100× stock):

   1. Dissolve 243 mg of adenine in 100 mL of 0.05 M HCl.

   2. Stir for approximately 1 h at room temperature (RT).

   3. Filter sterilize with 0.2 μm filters.

   4. Divide into 5 mL aliquots.

   5. Store at -20 °C.

      
      

2. Cholera enterotoxin (CT)

   Prepare 10 µM solution of cholera enterotoxin (this is 1,000× stock solution for 100 pM):

   1. Add 1.18 mL of Milli-Q water to a 1 mg vial of cholera enterotoxin to prepare a 10^-5 M solution.

   2. Dilute this in 110 mL of PBS.

   3. Filter sterilize with 0.2 µm filters.

   4. Aliquot 2 mL per cryovial.

   5. Store at -20 °C.

      Note: MW_CT = 84.000 Da

      
      

3. Hydrocortisone (HC)

   Prepare 0.2 mg/mL hydrocortisone (this is a 500× stock for 0.4 µg/mL):

   1. Dissolve a 25 mg vial in 5 mL of 100% ethanol. This solution is 5 mg/mL, which is 12.5× for 0.4 µg/mL. This can be stored at -20 °C indefinitely.

   2. Add 2 mL of this concentrated stock to 48 mL of sterile PBS + 0.1% BSA.

   3. Filter-sterilize with 0.2-µm filters.

   4. Aliquot 2 mL into cryovials.

   5. Store at -20 °C.

      
      

4. Epidermal growth factor (EGF)

   Prepare 10 µg/mL of EGF (this is a 50,000× stock for 0.2 ng/mL):

   1. Dissolve 100 µg of EGF in 10 mL of PBS + 0.1% BSA.

   2. Filter sterilize with 0.2 µm filters.

   3. Aliquot 1 mL into cryovials.

   4. Store at -20 °C.

      
      

5. Triiodothyronine (T3)

   Prepare 20 nM (2 × 10^-8 M) of T3 [this is a 1,000× stock for 20 pM (2 × 10^-11 M)]:

   1. Measure 6.8 mg of T3 and dissolve in 7.5 mL of 0.02N NaOH.

   2. Add 42.5 mL PBS (this is 100,000× for 20 pM T3).

   3. Store at -20 °C in 10 mL aliquots.

   4. To make the 1000× stock, dilute 0.4 mL of the 100,000× 1:100 into 39.6 mL of PBS.

   5. Filter sterilize with 0.2 µm filters.

   6. Divide into 2 mL aliquots.

   7. Store at -20 °C.

      
      

6. Calcium chloride (CaCl₂)

   Prepare using calcium dihydrate CaCl₂·2H₂O (this is a 1,000× stock for 0.3 mM):

   1. Dissolve 4.4 g of CaCl₂·2H₂O in 100 mL of Milli Q water.

   2. Stir with magnetic bar to dissolve completely.

   3. Filter sterilize with 0.2 µm filters.

   4. Aliquot 2 mL per cryovial.

   5. Store at -20 °C.

      
      

7. Insulin (1,000× for 5 µg/mL)

   Use insulin from bovine pancreas.

   1. Dissolve 100 mg of insulin in 20 mL of 0.005 M HCl in a 50 mL blue-capped tube.

   2. Filter sterilize through a celluloseacetate, lowprotein binding 0.2 µM filter.

   3. Aliquot 500 µL per tube.

   4. Store at -20 °C.

      
      

8. Sodium bicarbonate (71.2 mg/mL milliQ water)

   
   

For organotypic cultures

1. Keratinocyte serum free medium (K-SFM) complete

   Reagent	Final concentration	Quantity
   Keratinocyte-SFM	n/a	500 mL
   CaCl2 (1,000×)	0.3 mM	500 µL
   BPE (16.8 mg/mL)	25 µg/mL	750 µL
   EGF (10 µg/mL)	0.2 ng/mL	10 µL
   Total	n/a	501.26 mL

   Optional: Penicillin/Streptomycin can be added to K-SFM as well (100 U/mL).

   
   

2. Organotypic culture medium

   Reagent	Final concentration	Quantity
   DMEM	n/a	375 mL
   F12	n/a	125 mL
   Pen/Strep	100 U/mL	5.14 mL
   Adenine (2.4 mg/mL stock)	24 µg/mL	5.14 mL
   HC (0.2 mg/mL stock)	0.4 µg/mL	1 mL
   CT (10 µM stock)	100 pM	0.514 mL
   T3 (1,000×)	20 pM	0.514 mL
   Insulin (1,000×)	5 µg/mL	500 µL
   FCS	0.3%	1.54 mL
   Total		514.3 mL

   
   

3. DMEM 10% FBS (DMEM-10)

   Reagent	Final concentration	Quantity
   DMEM	n/a	445 mL
   FBS	10%	50 mL
   Pen/Strep	100 U/mL	5 mL
   Total		500 mL

   
   

Laboratory supplies

For organotypic tissue culture

1. Deep-well plates (Corning, catalog number: 355467)

2. Cell culture insert, PET membrane, 3.0 µm pore size (Corning, catalog number: 353092)

3. Airlift pads (cut in circles and autoclaved) (Whatman, GE Healthcare, catalog number: 10382461)

4. Cell culture Petri dishes or flasks from any brand (we use NUNC, Falcon, and Corning)

Equipment

For organotypic tissue culture

1. CO₂ incubator at 37 °C (any brand can be used)

2. Centrifuge (any brand, for 15 mL tubes and a minimum of 100 g)

3. Freezers (-20 °C and -80 °C)

   
   

Equipment and software for proteomics

1. KingFisher^TM Flex purification system (Thermo Scientific, catalog number: 5400610)

2. SpeedVac (Eppendor, model: Vacufuge^TM Concentrator)

3. Sonicator (Fisherbrand, model: 120 Sonic Dismembrator)

4. Spectrophotometer (Thermo Scientific, model: NanoDrop^TM 2000 C)

5. HPLC system [Thermo Scientific, model: UltiMate^TM 3000 Standard (SD)]

6. Evosep ONE (Evosep)

7. Mass spectrometer (Thermo Scientific, model: Orbitrap Exploris^TM 480)

8. Proteome Discoverer software v2.4 (Thermo Scientific)

9. Chromeleon software v7.2 (Thermo Fisher Scientific)

Procedure

Part I: Organotypic tissue culture

1. Preparing cells for organotypic cultures (day 1–5)

   1. Fibroblast cultures

      1. Culture fibroblasts (we use MRC-5 cells) until you have an 80%–90% confluent T75 flask. You will need 1.8 million fibroblasts for one tray of organotypic cultures. For most fibroblasts, you will need to seed 0.8 million fibroblasts three days in advance (see Figure 1).

         
         

         
         Figure 1. Fibroblasts suitable for organotypic collagen gels

         
         

      2. Trypsinize cells for 5 min and neutralize with an equal volume of DMEM with 10% FCS. Count the cells (only viable cells) and spin down.

      3. Resuspend fibroblasts at 8×10⁵ per milliliter of DMEM-10.

      4. Leave cells on ice while mixing the collagen gel.

         
         

2. Casting organotypic cultures

   Note: Make sure you have enough fibroblasts ready at this point. You will need 1.8 million cells.

   
   

   Acellular collagen gels

   Note: All solutions must be ice cold or placed on ice.

   For additional guidance watch Video 1.

   
   
   
   Video 1. How to make an organotypic culture

   
   

   1. Prepare a deep-well plate (6-well size) by adding one cell culture insert into each well. Use sterile forceps.

   2. In a 50 mL tube on ice, mix the following components without making air bubbles:

      1. 650 µL of 10× MEM

      2. 70 µL of L-glutamine (100× stock of 200 mM)

      3. 10 µL of gentamicin sulphate (40 mg/mL)

      4. 725 µL of fetal calf serum (FCS)

      5. 725 µL of sodium bicarbonate (71.2 mg/mL)

      6. 5.5 mL of rat tail collagen (4 mg/mL in 0.05% acetic acid) (homemade, see [12])

      7. 850 µL of DMEM with 10% FCS

      8. Add a few drops of 1 M NaOH to neutralize.

   3. Carefully pipette 1 mL of the acellular gel mixture from the previous step into the culture insert and make sure it covers the whole bottom of the insert. Leave to polymerize in the incubator while preparing the fibroblasts and the cellular gel. The gel will be polymerized after 10–15 min.

      
      

3. Making of cellular gel

   1. In a 50 mL tube on ice, mix the following components (avoid making air bubbles):

      1. 1.7 mL of 10× MEM

      2. 170 µL of L-glutamine (100× stock of 200 mM)

      3. 25 µL of gentamicin sulphate (40 mg/mL)

      4. 1.9 mL of FCS

      5. 525 µL of sodium bicarbonate (71.2 mg/mL)

      6. 14.4 mL of rat tail collagen (1 mg/ml in 0.05% acetic acid) (homemade)

      7. 2.1 mL of human fibroblasts (1.8 million cells) suspended in 10% calf serum DMEM

   2. Mix gently and add a few drops of 1 M NaOH to neutralize the solution (the color should change to orange/light pink).

   3. Quickly add 3 mL to the culture inserts on top of the acellular gel. Avoid air bubbles.

   4. Place the tray in the incubator for approximately 30 min; the gels will be fully polymerized.

   5. Fill DMEM 10% FCS in the well (18 mL) and 2 mL on top of the gel. Do not spray. See Figure 2 and Video 2.

      
      

      
      Figure 2. Casted organotypic collagen gels, ready for media to be added

      
      
      
      Video 2. How to fill media on organotypic cultures

      
      

4. Maturing collagen gels

   Four to six days after the gels are contracted and appear macroscopically as a slightly shrunken, white disk, they are ready for keratinocytes.

   Note: In our hands, this results in good organotypic cultures, possibly due to active deposition and reorganization of the ECM by fibroblasts.

   
   

5. Seeding keratinocytes on the casted collagen gels with fibroblasts (timing 2 h)

   1. Trypsinize N/TERT-1 cells to be seeded (WT and validated knock-outs) and adjust concentration to 1 × 10⁷ cells/mL (Figure 3).

      Note: 3 × 10⁵ cells need to be plated for each gel.

   2. Aspirate medium from the bottom of each well in the deep-well plate.

   3. Remove medium from the culture insert with a p1000 pipette.

      Critical: Avoid keeping the pipette too close to the gel inside the insert, as you may aspirate the gel.

   4. Add 30 µL of cell suspension (from step E1) in the center of the gel (Video 3).

      
      
      
      Video 3. Adding keratinocytes to organotypic cultures

      
      

   5. Add organotypic culture medium (see Recipes) at the bottom of the well in the deep-well plate until it reaches the bottom of the culture insert (∼9 mL).

   6. Incubate at 37 °C for 20 min to let the cells adhere.

   7. Add 2 mL of organotypic culture medium on top of the adhered cells and ∼16 mL of organotypic culture medium outside the insert and carefully place in the incubator. Do not spray as the keratinocytes will then detach.

   8. Incubate for four days before lifting the gels.

      
      

      
      Figure 3. Keratinocyte colonies. A. Colonies well-suited for organotypic collagen gels. B. Colonies not suited for organotypic cultures.

      
      

6. Air-liquid interface lifting of the keratinocyte. Timing: 30 min (Video 4)

   
   
   
   Video 4. Placing airlift pads

   
   

   1. On day 4 after seeding the keratinocytes, carefully aspirate medium from the culture inserts and from the plate wells.

   2. Place the insert into a sterile 100 mm dish using sterile forceps.

   3. Add two sterile airlift pads to the base of each well in the deep-well plate and place back the insert into the well over the pads.

   4. Add approximately 9 mL of organotypic culture medium in the deep wells until the pads are completely wet.

      Critical: The level of the medium should cover the pads and not be higher.

      
      

7. Adding inhibitors to organotypic cultures (Day 4–14)

   For experiments using different inhibitors, culture medium is supplemented with inhibitors in the desired concentration when the inserts are raised to the air-liquid interface. Concentration of the inhibitor is replenished with subsequent medium changes. Note that for some inhibitors, concentration needs to be raised compared to the use on 2D cultured cells. Add the desired inhibitor directly to the media in the well. Replenish with every media change.

   
   

8. Maturing of organotypic cultures

   Incubate the plate at 37 °C in a humidified incubator and change media in the deep wells every other day. Gels are ready to harvest in 10 days (Figure 4).

   
   

   
   Figure 4. Organotypic culture ready to be fixed. Arrow points to the concavity in the contracted collagen gel where keratinocytes are growing.

   
   

   Note: Organotypic cultures can now be fixed for histology or processed for western blot, RNAseq, or proteomics.

   
   

9. Formalin-fixed paraffin-embedded (FFPE) section processing

   Cut the membranes from the insert and place the 3D cultures in a histology cassette in 10% formalin for >24 h followed by paraffin embedding.

   
   

10. Frozen sections

    Note: The best morphology is obtained when the 3D cultures are incubated in 2 M sucrose (in dH₂O) for >48 h before embedding in Tissue-Tek and freezing in isopentane on dry ice.

    
    

    1. Cut the membranes from the insert and place the 3D cultures in a 2 M sucrose solution for >48 h.

    2. Freeze in isopentane on dry ice and keep at -80 °C until sectioning.

       Note: Sections cut at 4–6 μm give better staining results.

       
       

Part II: Proteomic analyses in 2D cell culture

Note: Steps K–P, Sample preparation for proteomics and phosphoproteomics and mass spectrometry analysis (2–3 days)

11. Cell lysis

    1. Cultivate N/TERT-1 cells in 2D until they reach 80% confluence. Approximately 1 million cells are needed.

    2. Lyse the cells by adding lysis buffer (500 μL) and boil the lysates for 10 min at 95 °C.

    3. Further lyse by micro-tip probe sonication for 2 min, pulsing 1 s on and 1 second off at 60% amplitude.

    4. Measure the protein concentrations using a BCA protein assay kit.

       
       

12. Protein digestion

    Note: Digest protein extracts overnight using the KingFisher Flex robot following the protein aggregation capture (PAC) method [13], adapted for a 96-well plate format (Figure 5).

    1. Dilute the lysates to a final concentration of 70% ACN.

    2. Add magnetic hydroxyl terminated beads for protein aggregation using a 1:2 protein/bead ratio. The amine beads can be replaced by hydroxyl-terminated beads.

    3. Wash proteins three times in 95% ACN and twice in 70% ethanol.

    4. Digest in 300 μL of 50 mM ABC with LysC and trypsin at enzyme/protein ratios of 1:500 and 1:250, respectively, for 12 h at 37 °C.

    5. Acidify samples with 50% TFA to a final concentration of 1% TFA.

    6. Clean the peptide mixtures on SepPak C18 1 cc Vac cartridge and elute with 300 μL of 40% ACN followed by 300 μL of 60% ACN.

    7. Evaporate the ACN in a SpeedVac.

    8. Estimate the final peptide concentration by measuring absorbance at 280 nm on a NanoDrop 2000 C spectrophotometer.

       
       

       
       Figure 5. Layout of the KingFisher plates for protein digestion

       
       

13. TMT labeling

    Note: Label peptides from each sample with TMTpro 16-plex Label Reagent. After labeling, 10 µg of pooled peptides is reserved for proteome samples and the rest is used for phosphopeptide enrichment.

    1. Add 1 M TEAB to each sample to reach a final concentration of 100 mM, followed by ACN to 50% final concentration.

    2. Incubate the labeled peptides with TMT reagents for 1 h at RT.

    3. Quench the reaction by adding 1% hydroxylamine (1:1 hydroxylamine/TMT) for 15 min at RT.

    4. Pool the samples and evaporate the ACN by SpeedVac.

       
       

14. Phosphopeptide enrichment

    1. Resuspend TMT-labeled peptides in 200 μL of loading buffer (Figure 6).

       
       

       
       Figure 6. Layout of the KingFisher plates for phosphopeptide enrichment

       
       

    2. Use Ti-IMAC beads in a 1:2 peptide/beads ratio and wash them in 500 μL of loading buffer for 5 min.

    3. Incubate the beads with the peptides for 20 min.

    4. Wash the beads successively with loading buffer, 80% ACN, 1% TFA, and finally 10% ACN and 0.2% TFA for 2 min each.

    5. Elute the phosphopeptides in 200 μL of 1% ammonia for 10 min.

    6. Repeat the enrichment process on the unbound remnant from the initial enrichment step with new elution buffers and beads.

       
       

15. Micro-flow high-pH reversed-phase peptide fractionation

    1. Resuspend TMT-labeled peptides in 50 mM ABC.

    2. Fractionate the peptides using a reversed-phase Acquity CSH C18 column on an UltiMate 3000 HPLC system with the Chromeleon software.

    3. Follow the provided multi-step gradient.

    4. Collect and concatenate to 12 fractions for phosphoproteome and 46 fractions for proteome, acidify with 10% formic acid, and dry with SpeedVac.

       
       

16. LC–MS/MS

    1. Analyze all samples by LC–MS/MS using the Evosep One system with pre-programmed gradients.

    2. MS settings:

       1. Spray voltage to 1.8 kV

       2. Heated capillary temperature at 275 °C

       3. Funnel RF level at 40

       4. Acquire data in profile mode with the full MS mass range set at 350–1,400 with an AGC target at 300%

       5. Set full MS resolution at 60,000 at m/z 200 with a maximum injection time of 25 ms

       6. Set the HCD fragment spectra resolution at 45,000 with an injection time of 86 ms and a Top10 method

       7. Set AGC target value at 200% and the intensity threshold at 2E5

       8. Isolation window set as at 0.8 m/z

       9. Normalized collision energy at 32%

Data analysis

Data analysis (proteomics)

All raw data files are analyzed using the Proteome Discoverer 2.4 software (developed by Thermo Fisher Scientific). The human SwissProt FASTA database, with 20,355 entries as of March 2019, was used as the reference protein database.

Trypsin was selected as the digestion enzyme. Up to two missed cleavages were permitted. TMTpro is specified as a fixed modification on lysine and peptide N terminus, and methionine oxidation is specified as a variable modification. In addition, phosphorylation is set as a variable modification on serine, threonine, and tyrosine residues in phosphoproteome samples.

Validation of protocol

Organotypic tissue culture

The human skin organotypic model with N/TERT-1 cells (WT cells and genetic engineered cells), or any other keratinocyte cell type or cancer cell type we have used, is very robust. In our laboratory, we have made more than 400 organotypic cultures with WT cells and more than 4,000 organotypic cultures during the last decades. The outcome varies with +/- 1 cell layer counted on >100 organotypic wildtype cell cultures. Furthermore, the phenotype of the 3D organotypic models is highly similar to the normal human skin (see Ye et al. [11], figure 7 below).

Figure 7. Comparison of normal human skin with 3D organotypic skin cultures. Top row: staining of human skin with differentiation markers [involucrin (INV), filaggrin (Flg), loricrin (Lor), keratin 10 (K10), and keratin 1 (K1)] and the proliferation marker Ki67. Lower row: the same staining in N/TERT-1 WT organotypic cultures. Statistical analysis, columns to the right, using one-way ANOVA followed by Dunnett’s multiple comparison test. The organotypic cultures show the same distribution of these markers as the normal skin, but the basal lamina will be straight compared to the wavy nature of the normal human skin.

General notes and troubleshooting

General notes

1. The 3D organotypic culture with keratinocytes and fibroblasts is very robust and reproducible.

2. The media is cheaper than premade media bought from different companies, although it is a little time-consuming to make all the stock solutions the first time.

3. The fact that we use 6-well plates makes it easy to have enough material for many different assays and also have enough good tissue for immunohistochemistry.

   
   

Troubleshooting

Acknowledgments

The work was supported by the European Commission (GlycoSkin H2020-ERC), European Commission (Imgene H2O20), Lundbeck Foundation, The Danish Research Councils (Sapere Aude Research Leader grant to H.H.W.), Danish National Research Foundation (DNRF107), the Friis Foundation (H.H.W AND S.D), Danish Strategic Research Council, and the program of excellence from the University of Copenhagen (CDO2016). We thank Karin Uch Hansen, Birgit Poulsen, Karen Biré, and Louise Rosgaard Duus for the excellent technical assistance. We acknowledge the Core Facility for Integrated Microscopy, Faculty of Health and Medical Sciences, University of Copenhagen. We would like to thank James G. Rheinwald, Harvard Institute of Medicine, for providing the N/TERT-1 cells.

This work was described in Ye et al. [11] and Dabelsteen et al. [2].

Competing interests

The authors have no financial or non-financial competing interests concerning this manuscript.

Ethical considerations

The two human cell lines used in this study were either bought at ATCC or provided by James G. Rheinwald, Harvard Institute of Medicine where the use for academic purposes is approved.

References

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