Materials and Reagents

Glass capillaries (World Precision Instruments, catalog number: TW100-4 )
PAP-pen (Ted Pella, catalog number: 22311 )
Pasteur glass pipettes (VWR, catalog number: 612-1702 )
Humidor made from large Petri dishes (145 mm) (Greiner Bio One International, catalog number: 639160 ) (Add wetted paper towel on the bottom of the dish to prevent mounted embryos from drying while injecting them.)
10 cm Petri dishes (Greiner Bio One International, catalog number: 633185 )
10 cm cell-culture dishes (Greiner Bio One International, catalog number: 664160 )
Normal glass microscopy slide (VWR, catalog number: 631-1551 )
Paper towel
Pipette tips (fitting for 100-1,000 μl, 20-200 μl, 2-50 μl and 0.5-10 μl pipettes)
FACS tubes with 40 μm mesh cap (BD, catalog number: 352235 )
15 ml tubes (Greiner Bio One International, catalog number: 188271 )
12-well plate (Greiner Bio One International, catalog number: 665180 )
Zebrafish (e.g., casper strain (roy-/-; mitfa-/-)
Tricaine (MS-222 or Ethyl 3-aminobenzoate methanesulfonate) (Sigma-Aldrich, catalog number: A5040 )
Low-melting-point agarose (Sigma-Aldrich, catalog number: A9414-10G )
Polyvinylpyrrolidone K 60 Solution, 45% (PVP) (Sigma-Aldrich, catalog number: 81430-500ML )
Phosphate buffered saline (PBS) (Biowest, catalog number: L0615-500 )
N-phenyl-thiourea (PTU) (Sigma-Aldrich, catalog number: P7629 )
Tris base (Sigma-Aldrich, catalog number: T1503 )
WM852 (RRID:CVCL_6804) transduced with p-lenti6 GFP lentivirus
Trypsin-EDTA solution (Lonza, catalog number: 17-161E )
Dulbecco's Modified Eagle Media (DMEM) (Sigma-Aldrich, catalog number: D6546 )
Pen-Strep solution (Sigma-Aldrich, catalog number: P0781 )
Fetal Calf Serum (FCS) (Thermo Fisher Scientific, Gibco^TM, catalog number: 10270106 )
NaCl (VWR, catalog number: 27810.295 )
KCl (VWR, catalog number: 26764.260 )
CaCl₂•2H₂O (Honeywell, Fluka^TM, catalog number: 31307-500G )
MgSO₄•6H₂O (Fisher Scientific, catalog number: 15640520)
Manufacturer: Honeywell, Fluka^TM, catalog number: M0250-500G .
60x E3 stock solution (see Recipes)
1x E3 (see Recipes)
E3 with 0.2 mM PTU (1x E3 + 0.2 mM PTU) (see Recipes)
20x Tricaine stock solution (4 g/L) (see Recipes)
1 M Tris-HCl, pH 9.0 (see Recipes)
1,000x PTU stock solution (0.2 M) (see Recipes)

Equipment

Pipettes (100-1000 ul, 20-200 ul, 2-50 ul, 0.5-10 ul)
Zebrafish housing system (e.g., AQUA SCHWARZ, model: Stand-alone unit V30 )
Mating boxes (e.g., AQUA SCHWARZ, model: SpawningBox 3 , catalog number: AS 006-0642)
Micropipette puller (NARISHIGE, catalog number: PB-7 ).
Fluorescence stereomicroscope (e.g., ZEISS, model: SteREO Lumar. V12 )
Micromanipulator (Eppendorf, model: InjectMan^® NI 2 , catalog number: 5181 000.017)
Microinjector, CellTramVario (Eppendorf, catalog number: 5176 000.033 )
CEDEX XS Cell counter (also Bürker chamber is perfectly adequate)
Incubator, 33 °C (no CO₂!!)
Forceps, Dumont No. 5 or similar (Sigma-Aldrich, catalog number: F6521 )
Pipette pump (Fisher Scientific, Fisherbrand^TM, catalog number: 15239805 )
Glass-tubing cutter (Sigma-Aldrich, catalog number: Z150770 )
Heating-block (Eppendorf, model: Thermomixer 5355 )
Vortex mixer (Scientific Instruments, model: Vortex-Genie 2 )
Centrifuge (Eppendorf, model: 5804 )

Software

ImageJ/FIJI (https://imagej.nih.gov/ij/download.html; https://fiji.sc/)
GraphPad Prism 6.0

Procedure

Preparing the embryos
1. Set-up mating two days before the injection day (Day 1). Three males and three females in a 3 L mating box are usually enough.
2. Collect embryos in the morning around 10:00 AM (Day 0) (The zebrafish mate when the lights turn on).
3. Select healthy fertilized embryos and place on separate 10 cm dishes–50 embryos/dish in 25 ml of 1x E3 + 0.2 mM PTU (see Recipes). Place in a 33 °C incubator (no CO₂!!) (Day 0).
4. On the injection day (Day 2), dissect the embryos out from the chorion membrane with fine sharp forceps (e.g., Dumont No. 5), if necessary. Many of the 2 dpf embryos may have hatched spontaneously (Figure 1).
  
  Figure 1. An unhatched embryo encased by chorion membrane (above) and a hatched embryo (below). Scale bar: 1 mm.
5. Anesthetize the embryos with 200 mg/L Tricaine (MS-222, 4 g/L stock solution) (see Recipes) for 5 min.
6. Melt aliquots of 0.7% low-melting point agarose (see Recipes) at 95 °C heating block. Let the block cool down to 37 °C before the next step.
  Note: Low-melting point agarose stays liquid at 37 °C.
7. Add 53 μl of 4 g/L Tricaine-stock solution into 1 ml of 0.7% low-melting point agarose (final concentration of agarose is 0.66%). Vortex briefly, and spin down. Place the tube back to 37 °C.
8. Prepare mounting slide. Take a normal glass microscopy slide and wipe it clean. Draw a bigger ellipse with a PAP-pen (for embryos) and a small circle (for 10 μl of cells) (Figure 2). Allow PAP-smear to dry for a couple of minutes. These hydrophobic linings will help to keep liquids in the correct place on the glass slide.
  
  Figure 2. Glass microscope slide with PAP-pen smears (faint greenish color)
9. Add 15 dechorionated and anesthetized embryos in the middle of the larger circle (Figure 3).
  
  Figure 3. Embryos in a droplet of E3 on the microscope slide
10. Add 200 μl of low-melting-point agarose and align the embryos gently using a gentle orientation tool (e.g., a pipette tip with a bit of attached nylon line) (Figure 4).
  
  Figure 4. Aligned embryos inside the agarose on a microscope slide. Orientation tool made of two pipette tips and a nylon line is in the front.
11. Allow the agarose to solidify. (The embryos stay alive within the agarose.) Store mounted embryos in a large (150 mm) humidified Petri dish (Figure 5), until ready to inject.
  
  Figure 5. A humidified Petri dish. Wetted paper towel is placed on the bottom of the Petri dish and covered with a lid. To prevent drying, the microscope slides with mounted embryos are placed in this chamber.
Preparing the cells
1. Use a 10 cm plate of GFP expressing tumor cells (50-90% confluent)/treatment.
2. Wash cells 2 times with PBS.
3. Aspirate PBS, add 3 ml of Trypsin-EDTA solution.
4. Incubate for 5 min at 37 °C, or until cells have detached.
5. Collect detached cells into a 15 ml Falcon tube and add 5 ml of DMEM + 10% FCS.
6. Pellet cells (180 x g), 3 min and resuspend in 10 ml of PBS.
7. Pellet cells (180 x g), 3 min and resuspend in 10 ml of PBS.
8. Pellet cells (180 x g), 3 min and resuspend in 1 ml of PBS.
9. Optional step, if using a cell line prone to clumping:
  1. Pipet the cell suspension into a FACS tube through a 40 μm mesh cap (BD Falcon).
  2. Pellet cells with a centrifuge for 3 min (180 x g).
10. Aspirate all liquid and resuspend the cells in 20 μl of 2% PVP/PBS injection solution. (Addition of PVP is optional, but helps to maintain stable cell suspension during injections.)
11. Count cell density (2 μl of cell suspension, 198 μl of PBS) using CEDEX XS cell counter.
12. Dilute into a final concentration of 3-10 x 10⁷ cells/ml. In 4 nl injection, this is 120-400 cells.
13. Store cell suspensions on ice until ready to inject.
Injection of tumor cells into embryos
1. Place an empty glass capillary needle (self-made capillary without filament, e.g., TW100-4, WPI) in CellTram injector. (Figure 6)
  
  Figure 6. Microinjection station
2. Break a large enough opening so that cells can be easily expelled (> 25 μm, a larger tip helps to get more cells in embryo but generates more damage to the embryo and is harder to get through the skin of the embryo) (Video 1).
  
  Video 1. Breaking the capillary needle
3. Gently rotate the oil outwards, until all air bubbles are out and oil comes out from the tip of the needle (Video 2).
  
  Video 2. Expelling the air bubbles
4. Gently touch the side of the tip with a paper tissue to absorb the excess oil.
  Note: The glass capillary is extremely fragile!
5. Add 10 μl of cell suspension in the smaller circle on the slide. Go to the injection work station.
6. Move the needle into cell suspension and draw some cell suspension into the needle (Video 3). Monitor under a stereomicroscope that some liquid and cells actually go into the needle and it doesn’t get stuck.
  
  Video 3. Filling the capillary needle. (Experimentation with zebrafish was performed under license ESAVI/9339/04.10.07/2016 issued by national Animal Experimentation Board (Regional State Administrative Agency for Southern Finland)).
7. Next, inject the embryos (Video 4). Move the needle through the skin of the embryo. Try to hit an empty space around the heart (pericardial cavity). Expel a little bit of cell suspension into the cavity (one fine notch with CellTram). Look that some cells actually went into the embryo and then move the needle out (Figure 7).
  
  Video 4. Injection of tumor cells into pericardiac space of the embryos. (Experimentation with zebrafish was performed under license ESAVI/9339/04.10.07/2016 issued by national Animal Experimentation Board (Regional State Administrative Agency for Southern Finland)).
  
  Figure 7. Embryos right after injection with GFP labeled tumor cells. Often some tumor cells escape from the injection site when the needle is withdrawn. Scale bar: 1 mm.
8. Move to the next embryo. Continue until all embryos are injected. In one session easily > 50 embryos can be injected.
9. After injections, discard the needle carefully according to your institutional guidelines.
10. Break the gel using fine forceps (Video 5) and by flushing the gel pieces into a dish with 1x E3-medium (Video 6) (see Recipes). Pipette up and down with a large bore Pasteur pipette to release the embryos from the gel (Video 7). Move the released embryos to a new Petri dish with fresh 1x E3 + 0.2 mM PTU (see Recipes).
  
  Video 5. Breaking the gel with forceps. (Experimentation with zebrafish was performed under license ESAVI/9339/04.10.07/2016 issued by national Animal Experimentation Board (Regional State Administrative Agency for Southern Finland)).
  
  Video 6. Releasing the gel pieces from the microscope slide. (Experimentation with zebrafish was performed under license ESAVI/9339/04.10.07/2016 issued by national Animal Experimentation Board (Regional State Administrative Agency for Southern Finland)).
  
  Video 7. Releasing the embryos from the gel. （Experimentation with zebrafish was performed under license ESAVI/9339/04.10.07/2016 issued by national Animal Experimentation Board (Regional State Administrative Agency for Southern Finland)）.
11. Add antibiotics (1:100 Pen-strep) and incubate 50 embryos/dish at 33 °C until transplanted embryos are selected for the experiment.
  Notes:
  1. Culturing the embryos at a higher temperature (33 °C) than usually (28.5 °C) facilitates the growth of human tumor cells in this model.
  2. Without a separate animal experiment license, the experiment has to be ended at latest when the embryos are 5 days old !!! Consult your Animal Experiment Board for details.
Imaging
1. At 1-day post-injection (1 dpi) anesthetize embryos with 200 mg/L Tricaine and select successfully transplanted and healthy embryos (Figure 8) under a stereomicroscope into the experiment.
  
  Figure 8. A healthy transplanted embryo. Scale bar: 1 mm.
2. Place 1 embryo/well in a 12-well plate with 2 ml of E3 + Tricaine, orient gently with an orientation tool and image both on GFP and bright field channels. After all the embryos have been imaged, aspirate excess medium out carefully and place 2 ml of fresh 1x E3 + 0.2 mM PTU medium in the wells. (Do not let the embryos dry!)
3. At 4 days post-injection anesthetize the embryos with tricaine again. Image embryos again using both GFP and bright field channels. (Figure 9)
  
  Figure 9. Timeline of the experiment and examples of the results. A. Time line of zebrafish xenograft experiments. B. Intravital fluorescence microscopy images of six dpf zebrafish embryos taken four days post injection (4 dpi). Fluorescence in GFP channel is shown. Scale bar, 500 µm. Inset shows magnification of the primary tumor. Tumor cells invading outside pericardial space are marked with an arrow, invading cells in the pericardial cavity with a triangle and unspecific fluorescence in eye and yolk sac with an asterisk (*). The outline of the pericardial cavity is depicted with dashed line. Figure and text reproduced and modified from Pekkonen et al. (2018).

Data analysis

In the image analyses, use ImageJ/FIJI software.
Subtract background (subtract background > rolling ball radius 25) in the GFP channel.
Outline the primary tumor area using a segmented line tool. Measure fluorescence intensity and shape (circularity) of the primary tumor.
Count manually the cells that have invaded outside the pericardial cavity. Adjust contrast/brightness so that you can see individual cells. These are much dimmer than the bright primary tumor.
Note: Autofluorescence is often observed in the lens and in the yolk.
For statistical analyses, use GraphPad Prism 6.0 software (other statistical software is ok too). Perform non-parametric Mann-Whitney (2 groups) or Kruskal-Wallis test (for > 2 groups).
For examples of the results, please see Figure 9b above and more detailed in Figure 7 in (Pekkonen et al., 2018).

Notes

For handling the embryos, a glass Pasteur pipette with a pipette pump works the best. The tip needs to be expanded by cutting it with a glass cutter for safe transport of embryos. Also, plastic Pasteur pipettes can be used.
Phenylthiourea (PTU) can be used to prevent pigmentation in non-albino zebrafish strains. PTU is neurotoxic → wear gloves and handle stock solution in chemical hood!
Xenograft assay also works with many other, but not all, cell types, melanoma cell line WM852 is used here as an example.
Sometimes the size of the implanted tumors may vary, if this turns out to be a problem, the relative tumor growth can be calculated and the number of invading cells normalized to the size of the primary tumor.
Due to technical and biological variability, a fairly large number of embryos (> 25) need to be xenografted and analyzed to gain robust results. This can be achieved by combining data from multiple independent experiments.
If one desires to implant a very large number of embryos (> 200/day), it is recommended to perform the experiment working as a pair. One researcher injects the embryos and the other one mounts and dismounts the xenografted embryos.
Embryos are fragile and can break easily. Avoid forceful handling and touching of embryos with sharp objects (other than the capillary needle).
Capillary needle is extremely sharp and filled with cancer cells. Caution is required so that the researcher doesn’t inject him/herself.
During low-resolution imaging with stereomicroscope, the mounting of anesthetized embryos is not necessary. If one desires to perform higher resolution imaging e.g., using confocal microscope, the mounting of embryos using low-melting point agarose on glass-bottom dishes is required.

Recipes

60x E3 stock solution (1 L) (Nüsslein-Volhard et al., 2002)
17.2 g NaCl
0.76 g KCl
2.9 g CaCl₂•2H₂O
4.9 g MgSO₄•7H₂O
1x E3
5 mM NaCl
0.17 mM KCl
0.33 mM CaCl₂•2H₂O
0.33 mM MgSO₄•7H₂O
Make by adding 16.67 ml of 60x stock solution into a 1 L vessel and fill up to 1 L with MilliQ water
E3 with 0.2 mM PTU (1x E3 + 0.2 mM PTU)
Add 1 ml of 1,000x PTU stock to 1,000 ml of E3
20x Tricaine stock solution (4 g/L)
Make by adding 4.0 g of Tricaine into a 1 L vessel and fill up to 1 L with 1x E3 medium
To adjust the pH to 7, add approximately 5 ml of Tris-HCl, pH 9.0
1 M Tris-HCl, pH 9.0
Make by adding 12.14 g of Tris into 100 ml vessel
Add 100 ml of MilliQ water and adjust the pH to 9.0 using HCl and/or NaOH
1,000x PTU stock solution (0.2 M)
3.044 g of PTU in 100 ml of ethanol
Note: This solution is toxic, store in an air-tight bottle.
0.7% low-melting point agarose
1. Add 0.7 g of low-melting point agarose powder into 100 ml of 1x E3 medium
2. Heat in microwave until agarose has melted and the solution is completely clear
3. Aliquot 1 ml of solution into 1.5 ml microcentrifuge tubes and store at -20 °C until used

Acknowledgments

This work was supported by the Centre of Excellence grant from the Academy of Finland (Translational Cancer Biology grant 307366; P.M.O., J.I.), Finnish Cancer Foundations (P.M.O.), Sigrid Juselius Foundation (P.M.O.), S.A. was supported by the Doctoral Program in Biomedicine (DPBM; University of Helsinki), and S.G. by the Academy of Finland grant 309544. The Zebrafish Core and Cell Imaging Core (Turku Centre for Biotechnology, University of Turku and Åbo Akademi University) are acknowledged.
These procedures have been evolved from the number of earlier work dealing with zebrafish embryo xenografting (Lee et al., 2005; Nicoli et al., 2007; Teng et al., 2013; White et al., 2013; Chapman et al., 2014; Veinotte et al., 2014; Xie et al., 2015; Yen et al., 2014).

Competing interests

The authors have no conflicts of interest or competing interests.

Ethics

Experimentation with zebrafish was performed under license ESAVI/9339/04.10.07/2016 issued by national Animal Experimentation Board (Regional State Administrative Agency for Southern Finland).

References

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Hogan, B. M. and Schulte-Merker, S. (2017). How to plumb a Pisces: Understanding vascular development and disease using zebrafish embryos. Dev Cell 42(6): 567-583.
Lee, L. M., Seftor, E. A., Bonde, G., Cornell, R. A. and Hendrix, M. J. (2005). The fate of human malignant melanoma cells transplanted into zebrafish embryos: assessment of migration and cell division in the absence of tumor formation. Dev Dyn 233(4): 1560-1570.
Nicoli, S., Ribatti, D., Cotelli, F. and Presta, M. (2007). Mammalian tumor xenografts induce neovascularization in zebrafish embryos. Cancer Res 67(7): 2927-2931.
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Xie, X., Ross, J. L., Cowell, J. K. and Teng, Y. (2015). The promise of zebrafish as a chemical screening tool in cancer therapy. Future Med Chem 7(11): 1395-1405.
Yen, J., White, R. M. and Stemple, D. L. (2014). Zebrafish models of cancer: progress and future challenges. Curr Opin Genet Dev 24: 38-45.