1Department of Hematology and Oncology, Children’s Hospital Boston, 2Harvard Stem Cell Institute, Harvard Medical School, 3Department of Medical Oncology, Dana Farber Cancer Institute
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Pugach, E. K., Li, P., White, R., Zon, L. Retro-orbital Injection in Adult Zebrafish. J. Vis. Exp. (34), e1645, doi:10.3791/1645 (2009).
Part 1. Preparation of injection material
Part 2. Injection
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.
Retro-orbital injection in adult zebrafish gives the highest efficiency of delivery of injected material to the bloodstream with the lowest incidence of mortality. Because of the nature of the injection spot, the puncture appears to heal quickly, decreasing the occurrence of infection and amount of blood loss. The site may even be repeatedly injected during a short time for daily injections of drugs, for example.
Large quantities of drugs must be purchased for traditional treatment methods in adult fish in which fish are simply immersed and soaked in water containing the drug of interest. However, if the drug is injected directly into the bloodstream of the animal, a much smaller quantity is required for treatment, thereby decreasing experimental costs. For certain compounds that are too large to enter the fish circulation through soaking, in the case of certain peptides, retro-orbital injection may also be advantageous.
Further, since RO injection is faster and easier than intracardiac injection techniques in the adult fish, another application of RO injection may include adult chemical genetic screening. Thus, retro-orbital injection may greatly facilitate zebrafish research requiring chemical or chemical delivery.
This work is supported by Howard Hughes Medical Institute and a grant from the NIH for the study of embryonic hematopoiesis.
|Heparin sodium salt from porcine intestinal mucosa||Sigma-Aldrich||2106||Preweighed vial of 300 USP units|
|Dulbecco’s Phosphate Buffered Saline||Invitrogen||14190-144|
|Dextran, Texas Red®||Molecular Probes, Life Technologies||D1830|
0.17 mM Kcl
0.33 mM CaCl2
0.33 mM MgSO2
|Microliter Syringe||Hamilton Co||80300||701N 10uL SYR (26s/2”/2)|