アダルトゼブラフィッシュにおける眼窩インジェクション

要約

ここでは、成人のゼブラフィッシュで眼窩の注入を行う方法を示しています。

要約

動物全体の薬物治療は、薬理学的および化学的遺伝学的研究の任意のモデルシステムに不可欠なツールです。静脈内（IV）注射は、多くの場合、関心のエージェントの配信の最も効果的かつ非侵襲的なフォームです。ゼブラフィッシュの（

プロトコル

Part 1. Preparation of injection material

1. Tg(globin:GFP) cells:
2. Bleed adult donor fish using 10ul pipette tip coated in heparin (1unit/ul) to puncture fish behind gill.
3. Aspirate red blood cells and dispense in cell buffer (0.9X PBS + 5% FBS + 1% Pen/Strep).
4. Filter cell suspension over 40uM mesh and determine concentration of cells using hemocytometer as previously described by LeBlanc et al.
5. Spin down and resuspend in cell buffer at desired concentration such that final injection volume is not more than 5ul. Here we inject 1.5-2 million cells/recipient.
6. For the dextran, Texas Red®, dissolve the dye in DPBS for a final injection concentration of 10-12 mg/mL. Plan to inject 4 uL per fish.

Part 2. Injection

1. Anesthetize fish in tricaine (4.2ml (4mg/ml) tricaine/100ml fish water).
2. Wash Hamilton syringe 3-4 times prior to injection using 70% ethanol. Rinse 3-4 times with 0.9X DPBS.
3. Place fish dorsal side up and facing right on damp sponge.
4. Hold the Hamilton syringe with your right hand and with your index finger on the plunger. Gently stabilize the body of the fish with your left hand.
5. Position the needle with the bevel facing up such that if the fish s eye were a clock, the needle would be pointing at the 7:00 position and at a 45 degree angle to the fish (figure 1).
6. Gently insert needle 1-2 mm into 7:00 position and slowly depress the plunger.
7. Allow the fish to recover in fresh E3 water.
8. Wash needle, as described above, between injections of different reagents.
9. Flick cell solution to resuspend cells every few minutes to prevent cell clumping.
10. Keep fish off flow for 1 week with daily water changes to avoid infection. We keep fish in ICU water for this period (10mL Stress coat + 5mL pemafix + 5mL melafix per 38 liters E3 water).

Part 3. Representative Results

When performed correctly, it is possible to visualize injected material if it has been labeled in some way. For example, Tg(globin:GFP) red blood cells should be seen under a fluorescent dissection microscope circulating in the vasculature of recipient casper fish soon after injection as shown in figure 2. Likewise, injection of a 70kDa dextran, conjugated to Texas Red® can be visualized in the vasculature of transparent fish immediately following retro-orbital injection (figure 3). Fluorescent kidney cells from Tg(β-actin:GFP) donor fish can also be injected retro-orbitally into irradiated casper recipient fish. These cells will eventually home to the recipient marrow (figure 4a) and may then go on to repopulate the kidney after several weeks (figure 4b).

If the injection is too shallow or the angle of the needle bypasses the retro-orbital venous sinus cavity, injected material may be visualized pooling around the eye or flowing out of it. Alternatively, if the injection is too deep, fish may experience tissue damage or excessive bleeding, though they may still recover. When performed correctly, mortality after retro-orbital injection should be less than 5% of total injected fish and success of delivery to the bloodstream should be greater than 90% of total injected fish.

Figure 1: Illustration of retro-orbital injection technique. The right eye of the fish is represented as an analogue clock in which the seven o clock position corresponds to the correct injection spot.

Figure 2: Tg(globin:GFP) red blood cells circulating in the vasculature of the tail of an adult casper fish three days after retro-orbital injection.

Figure 3: Successful injection of a 70kDa dextran conjugated to Texas Red® used as dye produces fluorescent vasculature in the transparent adult fish, casper and is readily viewed using standard whole animal fluorescence microscopy.

Figure 4a: Three days following retro-orbital injection of whole kidney marrow cells from Tg(β-actin:GFP) donor fish, the cells can be visualized homing to the kidney marrow of irradiated adult casper recipient fish.

Figure 4b: Four weeks following retro-orbital injection of whole kidney marrow cells from Tg(β-actin:GFP) donor fish, the repopulation of the recipient kidney with green donor whole kidney marrow cells can be visualized in irradiated adult casper recipient fish.

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ディスカッション

成人ゼブラフィッシュにおける眼窩注入は死亡率の最も低い発生率と血流に注入された材料の納入の最高効率が得られます。ために注射スポットの性質上、穿刺は感染症と失血の量の発生を減少させる、迅速に治癒に表示されます。サイトであっても繰り返して、例えば、薬物の毎日注射するための短い時間の間に注入されることがあります。

薬物の大量は、単純に浸?...

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資料

Name	Company	Catalog Number	Comments
Heparin sodium salt from porcine intestinal mucosa	Sigma-Aldrich	2106	Preweighed vial of 300 USP units
Tricaine-S	Western Chemical		MS-222
Dulbecco’s Phosphate Buffered Saline	Invitrogen	14190-144
Dextran, Texas Red®	Molecular Probes, Life Technologies	D1830
E3			5mM NaCl 0.17 mM Kcl 0.33 mM CaCl2 0.33 mM MgSO2
Microliter Syringe	Hamilton Co	80300	701N 10uL SYR (26s/2”/2)