Materials and Reagents

50 ml disposable syringe (Terumo, catalog number: SS-50ESZ )
Stainless steel surgical blade, No.10 (FEATHER Safety Razor, catalog number: No. 10 )
Plastic dish (9 cm diameter) (As One, catalog number: GD90-15 )
Glass capillary (1 x 90 mm, without filament) (Narishige, catalog number: G-1 )
Dissection needle: This is made by attaching 30 G needle (BD, catalog number: 305106 ) to a P1000 pipette chip (BM Equipment, catalog number: BIO1000RF ) whose tip is truncated (Figure 1)
Note: A handmade tool for removing the wound epidermis from the regenerate and for dissecting the blastema. This needle is different from that for transplantation (see Procedure B).

Figure 1. Dissection needle
Syringe filter unit (0.22 µm) (EMD Millipore, catalog number: SLGV033RB )
Zebrafish transplantation donor strain: Tg(Olactb:loxP-dsred2-loxP-egfp), which constitutively expresses the DsRed2 ubiquitously (Yoshinari et al., 2012). For simplicity, we refer the line as Tg(β-actin:dsred2) in this manuscript
Zebrafish transplantation host: a wild-type strain, which has been maintained in our facility by inbred breeding
Agarose (Nacalai Tesque, catalog number: 01028-85 )
Tricaine (3-aminobenzoic acid ethyl ester) (Sigma-Aldrich, catalog number: A5040 )
Fetal bovine serum (FBS) (any brand can be used)
Leibowitz’s L-15 medium (powder) (Thermo Fisher Scientific, Gibco^TM, catalog number: 41300070 )
1 M Tris-HCl (pH 9)
L-15 medium (see Recipes)
20x tricaine stock solution (see Recipes)

Equipment

Microwave oven
Micropipette puller (Sutter Instrument, model: P-97 )
Forceps
Glass dish (5 cm diameter)
Surgical blade handle (FEATHER Safety Razor, catalog number: No. 3 )
Microforge (Narishige, model: MF-900 )
Three-dimensional coarse manual manipulator (Narishhige, model: M-152 ) installed on a magnet stand
P20 micropipette
Fluorescence stereomicroscope

Procedure

Preparation of agar gel stage (Figure 2)
1. Mix agarose and water to make a 2% agarose solution and melt in a microwave oven.
2. Pour the melted agarose into a plastic dish up to a half of dish depth and leave at room temperature for 20-30 min.
3. Further fill the dish with the melted 2% agarose solution to approximately full depth and leave at room temperature for 20-30 min.
4. Make a rectangular well (2 x 4 cm square, 0.5 cm depth) at the center of gel stage by cutting and removing upper layer of the gel.
  
  Figure 2. Agarose gel stage
Preparation of transplantation needle
1. Pull the glass capillary with the micropipette puller to make a needle with a thin and long shaft. We routinely pull the glass capillary using the same conditions as for microinjection needles (our settings: heat 570, pull 150, velocity 120, time 60).
2. Set the pulled needle on the microforge, break the needle with forceps at a site where the inside diameter is approximately 20 μm. Make the end as blunt as possible with forceps. Using the microforge heater, make the needle end smooth and further make a harpoon.
  
  Figure 3. Transplantation needle. Scale bar = 50 μm.
Preparation of donor mesenchymal cells of whole regenerate including blastema (Video 1)

Video 1. Transplantation of mesenchymal cells including the blastema in regenerating zebrafish fin
1. Two days before transplantation, anaesthetize the donor zebrafish with 1x tricaine solution (~30 ml or enough volume to cover the fish body) in a plastic dish and cut their caudal fins with a scalpel. Note that the fins of host fish need to be amputated simultaneously. The amputated fish were returned to aquarium and normally fed until transplantation.
2. On the day of transplantation (2 days post amputation [dpa]), anaesthetize the donor fish with tricaine and cut the fin regenerate with a scalpel.
3. Transfer the fin regenerate with forceps to a glass dish containing 5-10 ml L-15 medium supplemented with 0.01% FBS.
4. Remove the wound epidermis from the regenerate (mesenchymal part) using the dissection needles as forceps. Peel the epidermis from the proximal side and remove the whole epidermis by gently pulling the epidermis from the edge as if taking off a T-shirt.
5. Divide the mesenchymal part of the regenerate to respective fin ray units. If necessary, the blastema can be further cut into smaller sizes.
Transplantation (Video 1)
1. Set the transplantation needle into the needle holder of manipulator.
2. Anaesthetize the host zebrafish with tricaine and place it on the agarose stage (Figure 4 and Figure 5).
  
  Figure 4. Zebrafish fin and the transplantation needle
  
  Figure 5. Microscope and manipulator set up
3. Make an opening on the surface of wound epidermis using the transplantation needle. Push the needle onto the regenerate surface and tap the head of manipulator knob to break the epidermis.
4. Transfer a piece of donor mesenchymal tissue including the blastema to site of the epidermal opening using a P20 micropipette.
5. Push the donor mesenchymal tissue with the transplantation needle to insert into the host regenerate. Hook the donor mesenchymal tissue with harpoon of the needle and force to insert into the host regenerate. Because proximal side of the donor mesenchyme is rigid, it is easier to hook the proximal side. Note that it is difficult to push the tissue with thinner needles. Transplantation can be performed for several fin rays at a time, but either of dorsal or ventral side of the fin should be blank as a regeneration control.
6. Put the operated fish back to aquarium (Figure 6).
  Notes:

Recipes

L-15 medium

Dissolve L-15 powder according to the manufacturer’s instruction
Sterilize through a 0.22-μm filter

20x tricaine stock solution

Dissolve 2 g of tricaine in 489.5 ml of distilled water
Add 10.5 ml 1 M Tris-HCl (pH 9) to bring the pH to 7
Store the solution in aliquots at -30 °C
Dilute the tricaine stock to 20 times with fish water to make 1x tricaine solution, which is used for anesthesia

Acknowledgments

This protocol was adapted from our previous works (Yoshinari et al., 2012; Shibata et al., 2016). The works were supported by the Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science (JSPS).

References

Shibata, E., Yokota, Y., Horita, N., Kudo, A., Abe, G., Kawakami, K. and Kawakami, A. (2016). Fgf signalling controls diverse aspects of fin regeneration. Development 143(16): 2920-2929.
Yoshinari, N., Ando, K., Kudo, A., Kinoshita, M. and Kawakami, A. (2012). Colored medaka and zebrafish: transgenics with ubiquitous and strong transgene expression driven by the medaka beta-actin promoter. Dev Growth Differ 54(9): 818-828.