发布: 2025年12月05日第15卷第23期 DOI: 10.21769/BioProtoc.5534 浏览次数: 608
评审: Ivonne SehringAnonymous reviewer(s)
Abstract
Zebrafish offer numerous advantages as a vertebrate model because of their rapid development, high fecundity, transparent embryos, and ease of genetic manipulation. A wide variety of transgenic and mutant fish lines have been generated, and efficiently sharing these resources is crucial for advancing research. Zebrafish lines have typically been exchanged as early embryos, adult fish, or cryopreserved sperm, making transportation costly and logistically challenging. Here, we provide a protocol for preserving functional zebrafish sperm for more than 7 days at room temperature and subsequent in vitro fertilization using the preserved sperm. In this protocol, sperm collected either from the cloaca of an anesthetized male or from dissected testes is stored in L-15-based storage medium. Importantly, the storage medium, originally developed for zebrafish, is also applicable to medaka, another widely used vertebrate model. This sperm storage method allows researchers to ship sperm using low-cost methods and to investigate key factors for motility and fertilizing ability in those sperm.
Key features
• Provides conditions for room-temperature preservation of zebrafish and medaka sperm for at least one week, based on Takemoto et al. [1].
• Introduces an in vitro fertilization method to achieve high fertilization rates with sperm samples preserved at room temperature.
• Enables the easy exchange of fish lines across countries via low-cost postal shipping.
Keywords: Zebrafish (斑马鱼)Graphical overview
Background
The zebrafish (Danio rerio) and medaka (Oryzias latipes) are phylogenetically distant teleost fish. Both are powerful vertebrate models in biological research due to their genetic tractability, rapid development, and optical transparency during early embryogenesis. Both serve as an important platform for research in developmental biology, genetics, disease modeling, and toxicology [2–5]. As zebrafish and medaka research expands globally, the need for reliable and efficient methods to manage and share genetic lines has grown increasingly important.
Traditionally, zebrafish lines have been distributed by shipping fertilized embryos. However, this approach has several limitations. Embryos are highly sensitive to environmental factors such as temperature, oxygen levels, and mechanical stress, which can compromise their viability and development during transport [6]. Additionally, embryos can only be maintained in a closed container at certain developmental stages for a limited period of up to 3 days (e.g., ZIRC, https://zebrafish.org/wiki/protocols/shipping), making long-distance or international shipping logistically challenging and often costly. Alternatively, cryopreservation has been used for long-term storage of sperm in many fish species [7–9]. However, sperm cryopreservation requires skilled techniques and maintenance of frozen conditions during transport. Specialized containers and administrative procedures are also necessary for the shipment of liquid nitrogen. Moreover, frozen samples are at high risk of being ruined by poor handling or shipping.
To overcome these challenges, we have developed a room-temperature sperm storage method [1] that allows storage for at least one week and retains ~32% fertilization efficiency even after 28 days under optimal conditions, thereby facilitating the transport of zebrafish genetic resources. When combined with in vitro fertilization (IVF) techniques, room-temperature sperm preservation provides a practical solution for sharing zebrafish lines. Fertilization using eggs from lab-stock females minimizes the risk of pathogen transmission between facilities, and stored sperm can be readily used to cross with locally maintained lines, enabling rapid experimental crosses. Moreover, this method facilitates studies on sperm quality––such as fertilization capacity and motility––and allows researchers to experimentally dissociate mating behavior from fertilization success, a critical distinction for understanding reproductive mechanisms. Here, we present detailed protocols for sperm preservation and its use in IVF in zebrafish. Notably, this sperm preservation method has been successfully applied to medaka, and corresponding protocols for medaka are described.
Materials and reagents
Biological materials
1. Adult zebrafish males and females
This protocol has been successfully used with the India strain (provided by Dr. Y. Kishimoto, National Institute of Genetics, Japan), the AB strain (provided by Dr. U. Strähle, Karlsruher Institute of Technology, Germany), the RW strain (provided by RIKEN, NBRP zebrafish), and their derivative transgenic and mutant lines. It could be applied to other zebrafish strains. Sexually mature males with a reddish body color and females with a fuller abdomen are suitable for sperm and egg collection, respectively.
2. Adult medaka males and females
This protocol has also been applied to the medaka OK-Cab strain (MT830-NIBB, provided by NBRP medaka), and other medaka strains could be used as well. Sexually mature males and females (4–6-month-old) exhibiting secondary sex characteristics in the anal and dorsal fins are suitable for sperm and egg collection. meioC loss-of-function mutants, in which germ cells arrest at the early stage of spermatogonia [10], can be used as infertile males to mate with wild-type females for the collection of unfertilized eggs.
Reagents
1. L-15 medium, Leibovitz (Sigma, catalog number: L5520)
2. Penicillin-Streptomycin, 5,000 U/mL (Gibco, catalog number: 15070-063)
3. D(+)-Glucose (Wako, catalog number: 041-00595)
4. Fetal bovine serum (FBS), Mexican origin (Sigma, catalog number: 173012, lot number: 0001653205)
5. Bovine serum albumin (BSA), fraction V, cell culture glade (Sigma, catalog number: A9418)
6. HEPES, suitable for cell culture (Sigma, catalog number: H4034)
7. L-(+)-Lactic acid (Sigma, catalog number: L6402-1G)
8. 1 M NaOH (Wako, catalog number: 196-05375)
9. Tricaine (3-amino benzoic acid ethylester) (Sigma, catalog number: A-5040)
10. NaCl (Wako, catalog number: 191-01665)
11. KCl (Wako, catalog number: 160-03555)
12. CaCl2·2H2O (Wako, catalog number: 031-00435)
13. MgSO4·7H2O (Wako, catalog number: 131-00405)
14. 0.82% methylene blue solution (Japan Pet Design, JAN code: 4975677045615)
15. 70% ethanol (Amakasu Chemical Industry, catalog number: NKH)
16. Bleach solution (Oyalox, JAN code: 4987038730016)
17. NaHCO3 (Wako, catalog number: 191-01305)
Solutions
1. 1 M HEPES-NaOH pH 7.9 (see Recipes)
2. 5% BSA (see Recipes)
3. 2 M glucose (see Recipes)
4. 1 M L-(+)-lactic acid (see Recipes)
5. 10 mM L-(+)-lactic acid (see Recipes)
6. Sperm preservation medium (see Recipes)
7. 500× tricaine (see Recipes)
8. 1× tricaine (see Recipes)
9. 50× E3 stock solution for zebrafish (see Recipes)
10. 1× E3 for zebrafish (see Recipes)
11. 20× solution A for medaka (see Recipes)
12. Solution B for medaka (see Recipes)
13. Balanced salt solution (BSS) for medaka (see Recipes)
Recipes
1. 1 M HEPES-NaOH pH 7.9
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| HEPES | 1 M | 23.83 g |
| 1 M NaOH | n/a | n/a |
| ddH2O | n/a | Fill to 100 mL |
Add 23.83 g of HEPES to ~80 mL of ddH2O. Dissolve completely. Adjust pH to 7.9 with 1 M NaOH. Make the volume to 100 mL with ddH2O. Filter sterilize using a 0.2 μm filter, aliquot, and store at -20 °C.
2. 5% BSA
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| BSA | 5% | 2.5 g |
| ddH2O | n/a | Fill to 50 mL |
Add 2.5 g of BSA to ~40 mL of ddH2O in a 50 mL conical tube. Allow the powder to settle without mixing to prevent clumping. Once the powder has swelled, gently mix by rotating the tube, then adjust the volume to 50 mL with ddH2O. Filter sterilize using a 0.2 µm filter, aliquot, and store at -20 °C.
3. 2 M glucose
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| D(+)-glucose | 2 M | 1.80 g |
| ddH2O | n/a | Fill to 5 mL |
Filter sterilize using a 0.2 μm filter and store at 4 °C. Warm up in a water bath if necessary.
4. 1 M L-(+)-lactic acid
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| L-(+)-lactic acid | 1 M | 90 mg |
| ddH2O | n/a | Up to 1 mL |
Filter sterilize using a 0.2 μm filter. Store at -20 °C.
5. 10 mM L-(+)-lactic acid
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| 1 M L-(+)-lactic acid | 10 mM | 10 μL |
| Autoclaved ddH2O | n/a | 990 μL |
| Total | n/a | 1 mL |
Prepare in a sterile condition. Store at -20 °C.
6. Sperm preservation medium
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| L-15 medium | n/a | 727.5 µL |
| Autoclaved ddH2O | n/a | 100 μL |
| 5% BSA (10×) | 0.5% | 100 μL |
| Penicillin-Streptomycin, 5,000 U/mL | 50 U/mL | 10 μL |
| 1 M HEPES, pH 7.9 | 10 mM | 10 μL |
| FBS | 3% | 30 μL |
| 2 M glucose | 25 mM | 12.5 μL |
| 10 mM L-(+)-lactic acid | 0.1 mM | 10 μL |
| Total | n/a | 1 mL |
Prepare on the day of sperm collection. Assemble all components in a sterile 1.5 mL tube on a clean bench. Ensure that the medium is prepared under sterile conditions to prevent contamination. The use of penicillin–streptomycin, which is commonly employed in cell culture media, is recommended as an antibiotic. Keep at room temperature (RT) until use.
7. 500× tricaine
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| Tricaine | 10% | 5.0 g |
| ddH2O | n/a | Up to 50 mL |
Store as 1 mL aliquots at -20 °C.
8. 1× tricaine
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| 500× Tricaine | 0.02% | 200 μL |
| Fresh fish water | n/a | 100 mL |
Prepare in a 100 mL plastic beaker on the day of use. Mix by agitating the cup gently.
9. 50× E3 stock solution for zebrafish
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| NaCl | 250 mM | 14.6 g |
| KCl | 8.5 mM | 0.63 g |
| CaCl2·2H2O | 16.5 mM | 2.43 g |
| MgSO4·7H2O | 16.5 mM | 4.07 g |
| 1 M NaOH | n/a | to pH 7.2 |
| dH2O | n/a | Up to 1 L |
Dissolve NaCl, KCl, CaCl2·2H2O, and MgSO4·7H2O in ~800 mL of dH2O. Adjust pH to 7.2 with 1 M NaOH. Autoclave and store at 4 °C.
10. 1× E3 for zebrafish
| Reagent | Final concentration | Quantity or volume |
| NaCl | 5 mM | 20 mL of 50× E3 stock solution |
| KCl | 0.17 mM | |
| CaCl2·2H2O | 0.33 mM | |
| MgSO4·7H2O | 0.33 mM | |
| 0.82% Methylene blue solution | 0.82 ppm | 100 µL |
| dH2O | n/a | Up to 1 L |
Store at RT. Stable for a week.
11. 20× solution A for medaka
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| NaCl | 2.2 M | 130 g |
| KCl | 107 mM | 8.0 g |
| CaCl2·2H2O | 27.2 mM | 4.0 g |
| MgSO4·7H2O | 16.2 mM | 4.0 g |
| dH2O | n/a | Up to 1 L |
Dissolve NaCl, KCl, CaCl2·2H2O, and MgSO4·7H2O in 1 L of dH2O. Autoclave and store at 4 °C.
12. Solution B for medaka
| Reagent | Final concentration | Quantity or volume |
|---|---|---|
| NaHCO3 | 600 mM (5%) | 2.5 g |
| ddH2O | n/a | Up to 50 mL |
Add 2.5 g of NaHCO3 to ~40 mL of ddH2O in a 50 mL conical tube. Gently mix by rotating the tube, then adjust the volume to 50 mL with ddH2O. Filter sterilize using a 0.2 µm filter.
13. Balanced salt solution (BSS) for medaka
| Reagent | Final concentration | Quantity or volume |
| NaCl | 111 mM | 50 mL of 20× solution A |
| KCl | 5.4 mM | |
| CaCl2·2H2O | 1.4 mM | |
| MgSO4·7H2O | 0.8 mM | |
| dH2O | n/a | Up to 1 L |
| NaHCO3 | 1.2 mM (0.01%) | 2 mL of solution B |
Dilute 20× solution A 20-fold with dH2O, autoclave, and adjust pH to 8.3 by adding solution B. Store at 4 °C.
Laboratory supplies
1. 1.5 mL tube (Watson, catalog number: 131-7155C)
2. Filtration disc with pore size of 0.2 μm (Advantec, catalog number: DISMIC-25CS)
3. 50 mL syringe, slip tip (Terumo, catalog number: SS-50ESZ)
4. 0.6 mL microtube (Watson, catalog number: 130-806C)
5. 1 mL syringe, slip tip (Terumo, catalog number: SS-01T)
6. 5 mL syringe, slip tip (Terumo, catalog number: SS-05SZ)
7. 50 mL syringe, slip tip (Terumo, catalog number: SS-50ESZ)
8. 10 μL tip (Watson, catalog number: 110-207C)
9. 200 μL tip (Watson, catalog number: 110-705C)
10. 1,000 μL tip (Watson, catalog number: 110-706C)
11. 90-mm Petri dish (BMBio, catalog number: BME-SNS0002)
12. Cellulose sponge (Nihon Insole Industry, no catalog number)
13. 100 mL plastic beaker (As One Corp., catalog number: I-100)
14. Plastic container
15. Membrane forceps (Advantec, catalog number: FS-1)
16. Cell counter plate, Burker-Turk (Watson, catalog number: 177-212C)
17. Microscissors (Roboz, model: RS-5803)
18. Tweezers, no. 5 Inox 08 (Dumont, model: 0108-5-PO)
19. Homogenizer pestle for 1.5 mL tube (BIO-BIK, catalog number: 1005-39)
20. Kimwipe (Nippon Paper Crecia, catalog number: S-200)
21. Paper towel (Konya Paper, catalog number: 4952137011014)
22. 24-well plate (Falcon®, catalog number: 351147)
23. 60-mm Petri dish (Iwaki, catalog number: 1010-060)
Equipment
1. Stereomicroscope with epi-illumination (Olympus, model: SZ61-SZ2-ILST)
2. Stereomicroscope with trans-illumination (Evident, model: SZ61-SZX2-ILTS)
3. Inverted or upright microscope equipped with a 40× objective lens (Nikon, model: Eclipse TE2000-S, or equivalent)
4. Incubator (PHCbi, model: MIR-154-PJ)
5. Timer (any)
Procedure
文章信息
稿件历史记录
提交日期: Sep 25, 2025
接收日期: Nov 2, 2025
在线发布日期: Nov 13, 2025
出版日期: Dec 5, 2025
版权信息
© 2025 The Author(s); This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
如何引用
Imai, Y., Asano, T., Nishimura, T., Takemoto, K., Kawamura, A. and Sakai, N. (2025). Room-Temperature Storage of Zebrafish and Medaka Sperm Using Lactic Acid-Stabilized L-15 Medium. Bio-protocol 15(23): e5534. DOI: 10.21769/BioProtoc.5534.
分类
生物科学 > 生物技术
生物工程 > 生物医学工程
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