Optimized Intravenous Injection in Adult Zebrafish

Summary

Here, we present an optimized and effective protocol for the intravenous injection of cells or pharmacological agents into adult zebrafish, resulting in enhanced cell engraftment and increased survival rates of the treated zebrafish.

Abstract

Intravenous (IV) injection is widely recognized as the most effective and commonly utilized method for achieving systemic delivery of substances in mammalian research models. However, its application in adult zebrafish for drug delivery, stem cell transplantation, and regenerative and cancer studies has been limited due to the challenges posed by their small body size and intricate blood vessels. To overcome these limitations, alternative injection techniques such as intracardiac and retro-orbital (RO) injection have been explored in the past for stem cell transplantation in adult zebrafish. However, these techniques have their drawbacks, including the need for meticulous injection techniques or increased risk of mortality.

In this study, we have developed a refined and optimized IV injection procedure specifically tailored to adult zebrafish, addressing the challenges associated with their unique anatomy. To demonstrate the effectiveness of this technique, we performed successful IV injections of whole kidney marrow cells from Tg(mpo: EGFP) fish and FITC-dextran dye into adult Casper fish. The subsequent visualization of injected cells and dyes using a fluorescence microscope confirmed their successful delivery and engraftment within the zebrafish. Furthermore, we demonstrated that compared with the intracardiac and RO injections, the IV injection resulted in improved survival rates and engraftment efficiency in treated zebrafish. This approach enables precise delivery and localization of substances and holds great potential for large-scale drug and chemical screening using adult zebrafish. Additionally, the ability to visually track the injected cells and dyes provides invaluable insights into their engraftment, migration, and interactions with host tissues, enabling a more comprehensive evaluation of therapeutic effects and biological processes in zebrafish models.

Introduction

Zebrafish (Danio rerio) has emerged as a valuable model organism in biomedical research, primarily due to its genetic similarity to humans, with more than 70% of human genes having zebrafish counterparts^1,2. This genetic resemblance, combined with zebrafish's compact size, rapid developmental cycle, and capacity for extensive genetic manipulation, makes it a powerful tool for scientific exploration. These attributes are particularly advantageous for experiments involving cell transplantation, drug delivery, and cell tracing. Furthermore, the optical clarity of transparent larvae and specific pigmentation mutants, such as the Casper zebrafish, allows for precise visualization of transplanted cells or substances, offering a more efficient and cost-effective alternative to traditional animal models.

Zebrafish are widely used to develop cancer transplantation models and to conduct drug screenings for severe diseases like glioma, melanoma, pancreatic tumors, and leukemia^{3,4,5,6,7,8,9,10}. Typically, these models are initiated at the larval stage to take advantage of the larvae's immature immune system and inherent transparency, which simplifies the injection process and enhances the feasibility of short-term studies. However, using larvae limits the duration for assessing engraftment and therapeutic interventions^7,11. Transitioning these experimental protocols to adult zebrafish introduces challenges such as more complex injection procedures, reduced engraftment efficiency, higher mortality rates, and increased variability in individual responses. These challenges highlight the critical need for improved injection and substance delivery techniques, particularly for studies involving adult zebrafish that require extended observation periods.

Historically, intracardiac¹² and retro-orbital (RO) injections¹³ have been the primary methods for drug delivery and cell transplantation in adult zebrafish. Intracardiac injection, which involves injecting substances directly into the heart, ensures immediate systemic circulation of drugs but is associated with significant risks, including potential cardiac injury and high mortality. On the other hand, RO injection, which delivers materials to the venous sinus behind the eye, also promotes rapid systemic distribution but can be stressful for the fish and demands high precision in execution¹⁴. IV injections, well-established for systemic substance delivery in mice and rats, are crucial for pharmacokinetics studies, drug efficacy assessments, and therapeutic interventions in these models^15,16,17,18. Recently, IV injections have gained prominence in zebrafish research, particularly in studies of innate immune responses^19,20 and acute kidney injury²¹ in larval zebrafish. However, their application in adult zebrafish remains limited.

In this study, we developed and optimized an IV injection procedure tailored specifically for adult zebrafish, which significantly improves survival rates, precision, and delivery efficiency. We visually demonstrate this method and provide a detailed protocol using this refined technique. We successfully administered IV injections of whole kidney marrow (WKM) cells from Tg(mpo: EGFP) fish and FITC-dextran dye into adult Casper fish, with confirmation of delivery and engraftment assessed by fluorescent microscopy. Our findings show that the refined IV injection technique is more efficient and consistent compared to the traditional intra-cardiac and RO methods. As the use of zebrafish in scientific research continues to expand, the adoption of this improved IV injection technique is likely to enhance our understanding of disease pathogenesis and accelerate the development of new therapeutic approaches.

Protocol

All animal procedures were approved by the Committee of the Use of Laboratory and Research Animals (CULATR) at the University of Hong Kong (HKU).

1. Preparation of injection material

1. Prepare cell suspension medium: 0.9x PBS + 5% fetal bovine serum (FBS) + 1% penicillin/streptomycin (Pen/Strep).
2. Sterilize the Hamilton syringe and attached needle (34 G, 10 mm length, 10 µL capacity, see Table of Materials) under UV light with a 270-280 nm wavelength and expose the items for 2 h.
3. Prepare sterilized cotton buds, foam pads, and tissue paper.
4. Prepare the anesthesia mixture by diluting tricaine with sterilized fish water to a final concentration of 0.2 mg/mL.
5. For the transplantation of WKM cells in Casper fish, 2 days before the transplantation, administer a sublethal irradiation dose of 25 Gy, divided into two sessions of 12.5 Gy each, given on the same day with a 7-8 h interval between doses. For the irradiation process, place 5-10 adult fish in a 100 mm Petri dish containing fish water and expose them in a gamma irradiator.
   NOTE: The dose was determined to be sublethal based on survival analysis after exposing Casper fish to various irradiation levels up to 35 Gy, monitored over 30 days (Figure 1A). The exact duration of exposure should be calibrated according to the settings of the irradiator. No irradiation is needed for procedures involving only drug delivery.
6. Use a laboratory autoclave steam sterilizer to sterilize the fish water intended for housing treated fish (see Table of Materials) to prevent infections and ensure a safe recovery environment for the fish post-injection.
   NOTE: The sterilization process is tailored to the specific autoclave unit used, and we adhere to the manufacturer's guidelines for autoclaving liquid solutions to prepare the fish water.
7. Prepare needle washing buffer: several tubes of 75% ethanol and ultrapure water in 1.5 mL microcentrifuge tubes.
8. Prepare transplantation buffer by dissolving FITC-Dextran (Molecular Weight: 10,000) in the previously prepared cell suspension medium (0.9x PBS with 5% FBS and 1% Pen/Strep). Adjust the concentration to 100 µg/mL.
   NOTE: This buffer will be used for the injections, with a planned volume of 2 µL per fish.

2. Preparation of whole kidney marrow for transplantation

1. Euthanize the necessary number of Tg(mpo: EGFP) fish by submerging them in a 0.4 mg/mL tricaine solution, ensuring they remain in the solution for at least 10 min following the cessation of opercular movement.
2. Dissect the Tg(mpo: EGFP) fish to isolate and transfer the kidney marrow (KM) into the cell suspension medium within a 1.5 mL microcentrifuge tube as described previously²².
3. Disaggregate the KM cells by pipetting and filtering the suspension through a 40 µm nylon cell strainer.
4. Centrifuge the suspension at 500 × g for 8 min.
5. Discard the supernatant and resuspend the pellet in 500 µL of cell suspension medium.
6. Count the cells using an automated counter with a 10 µL aliquot of the cell suspension.
7. Centrifuge again at 500 × g for 8 min.
8. Adjust the cell concentration to 150,000 cells/µL using the transplantation buffer.

3. Injection procedure

1. Thoroughly wash the Hamilton syringe 3-4x with 75% ethanol before the injection. Rinse the syringe 3-4x with ultrapure water to remove any ethanol residue.
2. Administer anesthesia to the zebrafish by immersing them in the anesthesia mixture until they are fully anesthetized, evidenced by diminished movement and loss of reflex responses. Once the fish are sedated, position them with their dorsal side facing upward and their head oriented to the left (Figure 1B). Carefully lay the fish on clean, damp tissue paper, which will help stabilize them for the injection. Make sure the tissue is sufficiently moist to prevent the fish from drying out, yet not so wet as to cause slipping.
3. Grasp the Hamilton syringe firmly and angle the needle at ~45° to the primary vessel (the caudal vein) to target it effectively while minimizing damage to surrounding tissues. For Capser zebrafish, aim for a section of the vessel that is visible through its translucent body for accurate needle placement (Figure 1B). For wild-type zebrafish (Tubingen, TU) with pigmented skin, aim for primary vessels which are along the body axis and posterior to the anus in the region of the primary vessels (Figure 1B). Gently and smoothly insert the needle into the designated vessel, administer the injection (2 µL) slowly to minimize stress, ensure optimal uptake of the substance, and apply gentle pressure to the site with a cotton bud for 10 s to control any bleeding after the injection.
4. Observe under a microscope to confirm the presence of GFP signals, ensuring the effectiveness of the injection. Confirm that the cells or dyes appear as green signals within the vessel (Figure 2A).
5. Allow the fish to recover in freshly sterilized fish water post injection for 10 min till transfer to a static tank.
6. Clean the needle as previously described between injections of different reagents.
7. To prevent cell clumping, flick the cell suspension every 10 min to resuspend the cells.
8. Maintain a maximum of 15 transplanted fish in a 4 L tank under static water conditions for the treatment duration. Alternatively, house the transplanted fish individually in 1 L static tanks. Equip the tank with an oxygen pump and perform daily water changes to minimize the risk of infection.
9. Monitor and assess GFP expression by flow cytometry in the fish approximately 14 days post-transplantation to evaluate the engraftment rate. Record the daily mortality of fish to accurately calculate survival rates. Perform one-way ANOVA for engraftment analysis and the Log-rank test for the survival analysis.

Results

To evaluate the effectiveness and precision of different injection methods in adult Casper fish, a comparative analysis was conducted using intracardiac, RO, and IV techniques (Figure 2A). Varying quantities of WKM cells from Tg(mpo: EGFP) fish were injected, each mixed with FITC-dextran dye at concentrations of 1 × 10⁵ and 3 × 10⁵ cells. The success of each method was determined through immediate microscopic assessment of GFP signal presence...

Discussion

In this study, we developed an IV injection protocol tailored for adult zebrafish to enhance the precision and consistency of delivering cells or drugs. A critical element of this method is the ability to localize and visualize the primary vein, which is crucial for the accurate administration of substances. While the translucent Casper zebrafish strain is recommended for optimal vessel visibility, our protocol is adaptable for use with various adult zebrafish strains, provided suitable adjustments are made for ...

Materials

Name	Company	Catalog Number	Comments
Autoclaves Steam Sterilizer	HIRAYAMA	HRG-140
Centrifuge 5424	Eppendorf
Countess 3 Automated Cell Counter	Thermofisher
Countess II FL	Invitrogen
Ethyl 3-aminobenzoate methanesulfonate salt (Tricaine)	Sigma-aldrich	MKCL9483
Falcon 40 µm Cell Strainer	CORNING		Blue, Sterile, Individually Packaged, 50/Case
FBS, Qualified	Gibco	26140079
FITC-Dextran (MW 10000)	MedChemExpress	60842-46-8
Injection needle	Hamilton	HAMI207434	34 G, 10 mm length
Micro syringe	Hamilton	7635-01	10 µL capacity, Model 701 RN
Nikon SMZ18
PBS pH 7.4 (1x)	Gibco	10010023
Penicillin-Streptomycin (5,000 U/mL)	Gibco™	15070063	100x
Pipette Tips	Eppendorf	epTIPS
Single Channel Pipette	Eppendorf	05-403-151
UltraPure Distilled Water	Invitrogen	10977015