Multiphoton Microscopy of FITC-labelled Fusobacterium nucleatum in a Mouse in vivo Model of Breast Cancer

Materials and Reagents

1. 1 mL syringe (BD Plastipak^TM, catalog number: 303084)

2. 27G and 26G needle (BD Plastipak^TM, catalog numbers: 305109 and 303176)

3. Sterile surgical pad

4. 10 cm tissue culture dish (Corning Incorporated, Falcon, catalog number: 353003)

5. 11 mL (Nunc^TM catalog number: 347856), 15 and 50 mL tubes (Miniplast, catalog numbers: 835-015-40-111 and 835-050-21-111)

6. 1.5 mL Eppendorf microtubes (Bar Naor Ltd., catalog number: BN022RL)

7. Scalpel (Bar Naor Ltd., catalog number: BN400-21-JH)

8. Whatman syringe filter 0.2 µm (Bar Naor Ltd., catalog number: BNFCA206030H)

9. Coverslip (Bar Naor Ltd., catalog number: BN1001-18-1CN)

10. Superfrost Plus glass slides (Thermo Fisher Scientific, catalog number: J1800AMNT)

11. Pipette tips [Axygen, catalog numbers: TF-200-R-S (20–200 μL), TF-1000-R-S (100–1,000 μL)]

12. Glass vials (Bar Naor Ltd., catalog number: BN1228WH)

13. Animals: 5–7-weeks-old female C57BL/6 mice (Envigo, Israel)

14. AT3 cell line (Sigma SCC178)

15. Dulbecco’s modified eagle medium (DMEM), 500 mL (Biological Industries, catalog number: 01-050-1A)

16. Accutase solution normal human, 100 mL (Biological Industries, catalog number: C-41310)

17. Dulbecco’s PBS, 500 mL (Biological Industries, catalog number: 02-020-1A)

18. Heat-inactivated fetal bovine serum (FBS), 500 mL (Biological Industries, catalog number: 04-127-1A)

19. L-glutamine in saline solution, 100 mL (Biological Industries, catalog number: 03-020-1B)

20. Penicillin–streptomycin solution, 100 mL (Biological Industries, catalog number: 03-031-1B)

21. MEM non-essential amino acids solution, 100 mL (Biological Industries, catalog number: 01-340-1B)

22. Fusobacterium nucleatum strain of interest (for example ATCC 23726)

23. Wilkins-Chalgren broth (Oxoid, catalog number: CM0643)

24. Fluorescein isothiocyanate (FITC), 1 g (Sigma-Aldrich, catalog number: F7250-1G)

25. Ethanol (Sigma-Aldrich, catalog number: E7023)

26. Trypan blue solution (Biological Industries, catalog number: 03-102-1B)

27. Sodium carbonate (Sigma-Aldrich, catalog number: 497-19-8)

28. Sodium hydroxide (Sigma-Aldrich, catalog number: 1310-73-2)

29. Isoflurane, USP Terrell^TM (Piramal, catalog number: VED1350)

30. Double deionized water (DDW)

31. Ice

32. Wilkins medium (see Recipes)

33. Sodium carbonate buffer (0.1 M, pH 9.0) (see Recipes)

34. FITC solution (see Recipes)

Equipment

1. Pipettes

2. Centrifuge (Eppendorf 5810 R)

3. Autoclave (Tuttnauer 2540MK)

4. Anesthesia induction chamber

5. Hemocytometer

6. Spectrophotometer (600 nm wavelength)

7. Orbital shaker

8. Nikon multiphoton A1MP

9. Stereo microscope (Nikon SMZ2-)

10. Scalpel handle

11. Scissors

12. Forceps

13. Tail vein injection platform

14. Heat lamp

15. Anaerobic chamber (Bactron I–II Shellab, USA)

16. Caliper

17. Vortex

Software

1. NIS-Elements (Nikon Instruments Inc.) https://www.microscope.healthcare.nikon.com/products/software/nis-elements)

Procedure

1. Prepare cells

   1. Seed 5 × 10⁵ AT3 cells in a 10 cm tissue culture dish in 10 mL of DMEM medium containing 10% heat-inactivated FBS, 1% L-glutamine, 1% penicillin–streptomycin, and 1% MEM non-essential amino acids solution. Incubate the cells at 37 °C in a humidified incubator with 5% CO₂ for 3–4 days. Ensure that the cells are 80%–100% confluent on the day of the experiment.

   2. Change media (DMEM supplemented with 10% heat-inactivated FBS, 1% L-glutamine, 1% penicillin–streptomycin, and 1% MEM non-essential amino acids solution) the day before implantation.

   3. To detach the tumor cells from the tissue culture dish, aspirate the culture medium, wash the cells with 5 mL of PBS, aspirate the PBS, and add 2 mL of accutase solution. Incubate the cells for 5–8 min with accutase at 37 °C. Trypsin/EDTA is an acceptable alternative to accutase.

   4. Add 3 mL of DMEM to neutralize the accutase and pipette up and down until all cells have been detached. Transfer the cells suspension to a 15 mL conical centrifuge tube and add 10 mL of medium (the same as in step A1).

   5. Centrifuge the cells at 1,000 rpm (200 × g) for 5 min at room temperature (RT). Aspirate the supernatant, leaving 500 μL of medium above the cell pellet. Resuspend the cells in the residual volume and add 10 mL of PBS. Invert the tube 2–3 times to get a homogeneous cell suspension and take 10 μL to count the cells in a hemocytometer. Use trypan blue to distinguish between live and dead cells.

   6. Centrifuge the cell suspension at 200 × g for 5 min at RT. Aspirate the PBS and resuspend the cells in PBS at a final concentration of 2 × 10⁶ cells/mL. Ensure that the single cell suspension has no clumping cells. Transfer the cells to an Eppendorf tube and keep on ice until use.




2. Orthotopical injection of AT3 tumor cells into mammary fat pad

   1. Anesthetize the mice in an induction chamber receiving a slow flow rate of isoflurane (3%–5% in oxygen).

   2. Place the mouse on a sterile surgical pad and make sure the head is properly placed inside the isoflurane nose cone. Confirm proper anesthesia by pinching the paw. Disinfect the injection site with 70% ethanol. Consider applying eye gel to prevent vision deterioration while the mouse is anesthetized.

   3. Inject subcutaneously 1 × 10⁶ AT3 cells in 50 μL of PBS orthotopically into the inguinal mammary fat pad using a 1 mL syringe with a 26G needle, by raising the nipple with forceps and inserting the needle underneath and perpendicular to the nipple.

   4. Monitor the mice until they regain consciousness; make sure they regain full consciousness before joining other mice.




3. Bacteria growth, staining, and injection to mice

   Perform bacterial injection when tumor size reaches 500 mm³ measured externally by caliper.

   1. Grow F. nucleatum strain of interest in 5 mL of sterile Wilkins medium (see Recipes) overnight for 12–18 h in an anaerobic chamber in an atmosphere of 90% N2, 5% CO₂, and 5% H₂ at 37 °C.

   2. Centrifuge at 2,057 × g for 5 min at 4 °C and discard supernatant. Resuspend the pellet with 1 mL of PBS, then add 4 mL of PBS and centrifuge again under the same conditions.

   3. Discard the supernatant and resuspend the pellet with 1 mL of a fresh FITC solution (see Recipes). Ensure that the single cell suspension has no clumps.

   4. Incubate in the dark with orbital rotation for 30 min at RT.

   5. Add 4 mL of PBS and suspend. Centrifuge at 2,057 × g for 5 min at 4 °C and repeat the washing until the PBS in the supernatant is clear.

   6. Discard the supernatant, resuspend the bacteria with 1 mL of PBS, and bring the bacteria to an OD₆₀₀ of 1 (approximately 1 × 10⁹ bacteria/mL). Keep bacteria on ice and in the dark until use.

   7. Restrain the mouse in a tail vein injection platform. Position the tail such that the vein is facing upwards.

   8. Prior to injection, warm the tail using an overhead heat lamp for a few minutes to dilate the veins.

   9. Using a 1 mL syringe and a 27G needle, insert the needle gently, while the bevel is up, into the lateral or dorsal tail vein towards the direction of the head. Keep the needle and syringe parallel to the tail. Inject intravenously 5 × 10⁷ fluorescein-5-isothiocyanate (FITC)-labeled F. nucleatum ATCC 23726. The contents of the needle should inject easily without resistance. In order to confirm correct intravenous injection, the piston should easily move and the vein color should change to a whiter color momentaneously.




4. Mice sacrifice and tissue harvesting

   1. Twenty-four hours after bacterial injection, transfer mice to a chamber containing 2% isoflurane in oxygen for approximately 30 s.

   2. Verify that mice are fully anesthetized and perform cervical dislocation. Another option is performing CO₂ euthanasia followed by confirmation by cervical dislocation.

   3. Clean tumor area with 70% ethanol. Cut the skin with a pair of sterilized scissors in the ventral middle of the mice, near the tumor. Hold the skin near the tumor with sterile forceps and remove tumor carefully using a sterile scalpel.

   4. Hold the skin on the other side of the mice’s body near the healthy (control) breast tissue with sterile forceps and remove tissue carefully using a sterilized scalpel.

   5. Place tumor and healthy breast tissue in a glass vial containing PBS, on ice.




5. Multiphoton microscopy of FITC-labeled F. nucleatum

   1. Cut a slice from the fresh tissue using a scalpel and photograph using a Nikon SMZ25. Representative images are shown in Figure 1.

      
      

      
      Figure 1. Nikon SMZ25 images of breast cancer tissue and adjacent mammary tissue. Representative microscopy images of tumor and normal adjacent mammary samples harvested 24 h post intravenous injection of 5 × 10⁷ FITC-labeled F. nucleatum ATCC 23726 or with PBS vehicle into AT3 cancer-bearing mice.

      
      

   2. Place the tissue on a slide with a drop of water and cover with a coverslip.

   3. Observe and photograph immunofluorescent images using the Nikon multiphoton A1MP microscope set to 740 nm wavelength using a 25× objective. Representative images are shown in Figure 2.

      
      

      
      Figure 2. Nikon multiphoton A1MP microscope images of breast cancer tissue and adjacent mammary tissue. Representative multiphoton microscopy images of tumor and normal adjacent mammary samples harvested 24 h post intravenous injection of AT3 cancer-bearing mice with 5 × 10⁷ FITC-labeled F. nucleatum ATCC 23726. Images were taken from Parhi et al. (2020). No changes were made.

Data analysis

Images obtained from the fluorescence microscope are converted to 8-bit images by NIS-Elements software (see Figures 1 and 2).

Recipes

1. Wilkins medium

   100 mL of DDW

   3.1 g of Wilkins-Chalgren broth

   Mix until dissolved

   Autoclave at 121 °C for 30 min and aliquot 5 mL to 11 mL tube

   Reduce in an anaerobic chamber overnight




2. Sodium carbonate buffer (0.1 M, pH 9.0)

   84 mg of sodium carbonate

   10 mL of DDW

   Adjust pH to 9.0 with sodium hydroxide

   Sterilize by filtering through 0.2 μm Whatman filter




3. FITC solution

   Dissolve 1 mg of FITC in 10 mL of sodium carbonate buffer by vortexing

   Keep in the dark until used

Acknowledgments

The authors thank Dr. Zakhariya Manevitch for his valuable help in microscopy. This work was supported by the Israel Cancer Research Fund Project grant and the Israel Science Foundation Moked grant. This protocol was derived from Parhi et al. (2020). Nature Communications. https://doi.org/10.1038/s41467-020-16967-2

Competing interests

The authors declare no competing interests.

Ethics

Experiments were carried out under protocol MD-17-15239-5 approved by the Hebrew University of Jerusalem Ethics Committee and signed by the chairperson Prof. Sara Eyal.

References

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