Method for culturing fish germline stem cells

Abstract

To provide a novel method for culturing fish germ stem cells in large quantity and stably.SOLUTION: The present invention provides a culture method for fish germ stem cells, comprising culturing, on a surface coated with vitronectin, fish germ stem cells in a culture medium including the eight components below: (1) insulin, (2) selenium, (3) transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO3 or KHCO3, and (8) L-glutamine.SELECTED DRAWING: None

Description

[Technical Field]

[0001] This invention relates to a method for culturing fish germline stem cells, and more specifically, to a method for culturing fish germline stem cells under serum-free and feeder-free conditions. [Background technology]

[0002] With the accelerating global population growth, a serious food shortage is anticipated in the future. One approach to addressing this problem has recently attracted attention to developing efficient methods for the production and management of marine resources.

[0003] One way to enable the efficient production of fish and shellfish resources is to breed varieties that grow quickly and varieties that have strong resistance to disease.

[0004] One way to efficiently breed such desirable fish and shellfish varieties is to use genetic modification techniques, as is done in the animal sector (Non-Patent Literature 1). However, this approach requires technology to maintain and propagate fish and shellfish germ stem cells in large quantities and stably.

[0005] However, compared to the animal sector, the technology for mass-producing and stably cultivating germline stem cells is not yet fully established in the fish and shellfish sector. [Prior art documents] [Non-patent literature]

[0006] [Non-Patent Document 1] Yoshiko Iwasaki-Takahashi et al. Commun Biol. 2020 Jun 15;3(1):308. [Overview of the Initiative] [Problems that the invention aims to solve]

[0007] In view of the above situation, an object of the present invention is to provide a novel method for culturing fish germ stem cells in large quantities and stably. [Means for Solving the Problems]

[0008] As a result of intensive studies on the above problems, the present inventors found that when culturing fish germ stem cells on a surface coated with vitronectin in a medium containing specific 8 components, the stem cells efficiently proliferated while maintaining their stem cell properties well even under serum-free and feeder-free conditions. Based on such findings, the present invention was completed by further advancing the research. That is, the present invention is as follows.

[0009] [1] A method for culturing fish germ stem cells, comprising culturing fish germ stem cells on a surface coated with vitronectin in a medium containing the following 8 components: (1) Insulin, (2) Selenium, (3) Transferrin, (4) L-Ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO3 or KHCO3, (8) L-Glutamine. [2] The method according to [1], wherein the medium is a serum-free medium. [3] The method according to [1] or [2], which is carried out under feeder-free conditions. [4] When subculturing, 0.5×10 , , , , 5 , , , 2 , 5 , , ~6.5×10 5 Cells / cm 2 The method according to any one of [1] to [3], comprising a step of reseeding. [5] A kit for culturing fish germ stem cells, comprising: Vitronectin, and The following 8 components: (1) Insulin, (2) Selenium, (3) Transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO3 or KHCO3, (8) L-glutamine. [6] The kit described in [5] further includes a basal culture medium. [7] The kit according to [5] or [6], further comprising sodium chloride when (7) is KHCO3. [Effects of the Invention]

[0010] According to the present invention, fish germline stem cells can be proliferated very efficiently while maintaining their stem cell properties well under serum-free and feeder-free conditions. [Brief explanation of the drawing]

[0011] [Figure 1] Figure 1 shows a photograph of germline stem cells after alkaline phosphatase staining (AP stain) (upper left), and the percentage of CD90.2-positive germline stem cells when mackerel germline stem cells were cultured in DMEM or L15 medium supplemented with various components, with or without the presence of vitronectin (mediums 1-5 (DMEM or L15), upper bar graph: cell count at seeding 6.5 × 10⁵ cells, lower bar graph: cell count at seeding 25 × 10⁵ cells). [Figure 2] Figure 2 shows the percentage of stem cell properties of germline stem cells after culturing when germline stem cells of mackerel were cultured in media 1-5 (DMEM or L15) with varying cell numbers at seeding. [Figure 3] Figure 3 shows the doubling time of germline stem cells when mackerel germline stem cells were cultured in media 1-5 (DMEM or L15) with varying cell numbers at seeding. [Figure 4]Figure 4 shows the viability, confluency, and CFU of mackerel germ stem cells cultured in media 1-5 (DMEM only) with varying cell numbers at seeding. [Figure 5] Figure 5 shows the results of observing the cell number, doubling time, confluent region, stem cell characteristics, and viability over a 4-day period when the cell density was changed during subculturing of germline stem cells of mackerel using medium 4 (DMEM / vitronectin coated). [Figure 6] Figure 6 shows photographs of mackerel germline stem cells cultured in medium 4 (DMEM / vitronectin coated) after 4 days of subculturing, where the cell density was altered during subculturing. [Figure 7] Figure 7 is a graph showing the proliferation efficiency of germline stem cells extracted from female and male mackerel when cultured in a medium containing eight specific components and under conditions of a vitronectin coating. [Figure 8] Figure 8 shows photographs illustrating the expression of various cell markers (CD90.2, KLF4, SOX2, Oct4, GFR1a, and Vasa) when germline stem cells extracted from female mackerel were cultured in a medium containing eight specific components and under conditions of a vitronectin coating. [Figure 9] Figure 9 shows the stem cell properties and viability of germline stem cells of medaka fish cultured under various conditions. [Figure 10] Figure 10 shows that in the culture of fish germline stem cells, NaHCO3 added to DMEM medium can be substituted with KHCO3. [Figure 11] Figure 11 is a graph showing the stem cell properties and doubling time when the cell density during passage is changed under each condition of Example 7. [Figure 12] Figure 12 is a graph showing the viability, confluence, and CFU of fish germline stem cells under each condition of Example 9. [Figure 13]Figure 13 is a graph showing the stem cell properties and survival rate when germline stem cells of medaka and mackerel are cultured under various conditions. [Figure 14] Figure 14 shows graphs of cell number, population doubling time, confluent area, stem cell properties, and viability when mackerel germ stem cells were cultured at four different cell densities using Media C and vitronectin. [Figure 15] Figure 15 is a photograph of cell populations when mackerel germline stem cells were cultured at four different cell densities using Media C and vitronectin. [Figure 16] Figure 16 shows graphs of cell number, population doubling time, stemness, and viability when mackerel germ stem cells were cultured at four different cell densities using Media N and vitronectin. [Figure 17] Figure 17 shows that the culture medium (FSC10), which is Media N with added selenium and sodium chloride (NaCl), is superior to Media N in terms of stem cell characteristics, viability, mortality, confluence, and colony number. [Figure 18] Figure 18 shows the preferred concentration range for the active ingredient of FSC10. [Modes for carrying out the invention]

[0012] The present invention will be described in detail below.

[0013] 1. Method for culturing fish germline stem cells The present invention provides a method for culturing fish germline stem cells (hereinafter sometimes referred to as "the method of the present invention"), which comprises culturing fish germline stem cells on a surface coated with vitronectin in a culture medium containing eight specific components ((1) insulin, (2) selenium, (3) transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO3 or KHCO3, and (8) L-glutamine).

[0014] In the method of the present invention, the eight components contained in the culture medium can all be produced by known methods or commercially available products may be used. The species from which insulin, transferrin, FGF2, and TGFβ are derived are not particularly limited as long as the desired effects of the present invention are obtained, but are preferably human. Furthermore, these components may be of biological origin or recombinant proteins. If (7) is NaHCO3, it is a mixture of components (1) to (8), and commercially available Essential 8 TM It is also preferable to use supplements (Thermo Scientific, Catalogue no. A1517001).

[0015] The amounts of these eight components added to the culture medium are not particularly limited as long as the desired effects of the present invention are obtained, but in one embodiment, the following amounts may be used. (1) Insulin: 0.1-200 mg / L (preferably 1-150 mg / L, 5-100 mg / L, 5-90 mg / L, 10-80 mg / L, or 10-70 mg / L) (2) Selenium: 0.1 to 100 μg / L (preferably 1 to 90 μg / L, 5 to 80 μg / L, 5 to 70 μg / L, 10 to 60 μg / L, or 10 to 50 μg / L) (3) Transferrin: 0.1 to 200 mg / L (preferably 1 to 150 mg / L, 1 to 100 mg / L, 1 to 90 mg / L, 5 to 80 mg / L, or 5 to 70 mg / L) (4) L-ascorbic acid: 1-500 mg / L (preferably 1-400 mg / L, 5-300 mg / L, 10-250 mg / L, 10-200 mg / L, or 10-150 mg / L) (5) FGF2: 1-500 μg / L (preferably 1-400 μg / L, 5-350 μg / L, 10-300 μg / L, 20-250 μg / L, or 50-250 μg / L) (6) TGFβ: 0.01~20 μg / L (preferably 0.1~10 μg / L, 0.5~10 μg / L, 0.5~8 μg / L, 0.7~8 μg / L, or 0.8~6 μg / L) (7) NaHCO3: 0.01~20 g / L (preferably 0.1~10 g / L, 0.5~10 g / L, 0.5~8 g / L, 0.7~8 g / L, or 0.8~6 g / L) (8) L-Glutamine: 1-500 mg / L (preferably 1-400 mg / L, 5-350 mg / L, 10-300 mg / L, 20-250 mg / L, or 50-250 mg / L) In one embodiment, NaHCO3 can be substituted with the same amount of KHCO3.

[0016] In another embodiment, when KHCO3 is used in the method of the present invention, it is preferable to add sodium chloride (NaCl). The following concentrations are suitable as examples of NaCl addition: (1) Insulin: 10-60 mg / L (preferably 10-58 mg / L, 10-50 mg / L, 11-45 mg / L, 15-30 mg / L, or 15-25 mg / L) (2) Selenium: 11-63 μg / L (preferably 13-60 μg / L, 15-50 μg / L, 17-40 μg / L, 18-30 μg / L, or 19-25 μg / L) (3) Transferrin: 5-32 mg / L (preferably 5.5-30 mg / L, 5.5-28 mg / L, 6-26 mg / L, 8-25 mg / L, or 9-15 mg / L) (4) L-ascorbic acid: 32-192 mg / L (preferably 40-150 mg / L, 45-100 mg / L, 50-90 mg / L, 55-80 mg / L, or 57-75 mg / L) (5) FGF2: 50-300 μg / L (preferably 60-200 μg / L, 70-180 μg / L, 75-150 μg / L, 80-120 μg / L, or 90-110 μg / L) (6) TGFβ: 1-6 μg / L (preferably 1.1-5 μg / L, 1.5-4 μg / L, 1.6-3.5 μg / L, 1.7-2.8 μg / L, or 1.8-2.6 μg / L) (7) KHCO3: 1.36~2.15 g / L (preferably 1.4~2.00 g / L, 1.5~1.90 g / L, 1.5~1.85 g / L, 1.6~1.83 g / L, or 1.65~1.80 g / L) (8) L-Glutamine: 50-300 mg / L (preferably 60-200 mg / L, 80-180 mg / L, 70-150 mg / L, 80-120 mg / L, or 90-110 mg / L) (9) NaCl: 60.5-363 mg / L (preferably 65-350 mg / L, 80-300 mg / L, 90-200 mg / L, 100-150 mg / L, or 110-130 mg / L)

[0017] Furthermore, the vitronectin (or a fragment of vitronectin, as long as its function is maintained) used in the present invention may be manufactured by a method known to the present, or a commercially available product may be used. The species from which the vitronectin or its fragment originates is not particularly limited as long as the desired effects of the present invention are obtained, but it is preferably human.

[0018] The coating of culture vessels such as wells and dishes with vitronectin can also be carried out by known methods. For example, by dispensing PBS containing dispersed vitronectin into a culture vessel and incubating it at 37°C for 1 hour, the inner surface of the culture vessel can be coated with vitronectin.

[0019] The culture medium that can be used in the method of the present invention is not particularly limited as long as the desired effects of the present invention are obtained, and any basal medium can be used. In one embodiment, the following media can be preferably used: Dulbecco's Modified Eagle's Medium (DMEM), Ham's Nutrient Mixture F12, DMEM / F12 medium, McCoy's 5A medium, Eagle's Minimum Essential Medium (EMEM), alpha Modified Eagle's Minimum Essential Medium (αMEM), MEM medium (Minimum Essential Medium), RPMI1640 medium, Iscove's Modified Dulbecco's Medium;IMDM), MCDB131 medium, William's medium E, IPL41 medium, Fischer's medium, StemPro34 (Invitrogen), X-VIVO 10 (Kambrex), X-VIVO 15 (Kambrex), HPGM (Kambrex), StemSpan H3000 (Stem Cell Technologies), StemSpanSFEM (Stem Cell Technologies), StemlineII (Sigma-Aldrich), QBSF-60 (Quality Biological), StemProhESCSFM (Invitrogen), Essential6® medium (Gibco), Essential8® medium (Gibco), Essential8® Flex medium (Thermo Fisher), StemFlex medium (Thermo Fisher), StemScale® PSC Suspension Medium (Thermo Fisher), mTeSR1 or 2 or Plus medium (Stem Cell Technologies), Repro FF or Repro FF2 (ReproCELL), PSGro hESC / iPSC medium (System Biosciences), NutriStem® medium (Biological Industries), MSC NutriStem® XF Medium (Biological Industries), CSTI-7 medium (Cell Science Institute), MesenPRO RS medium (Gibco), MF-Medium® mesenchymal stem cell growth medium (Toyobo Co., Ltd.), serum-free mesenchymal stem cell medium (Fukoku Co., Ltd.), Mesenchymal Stem Cell Growth Medium Examples include 2 (PromoCell), Sf-900II (Invitrogen), Opti-Pro (Invitrogen), StemFit® AK02N or Basic02 or AK03N or Basic03 or Basic04 medium (Ajinomoto Healthy Supply Co., Ltd.), STEMUP medium (Nissan Chemical Corporation), and L15 medium. Preferably, it may be DMEM / F12 (Ham) 1:1 medium.

[0020] In some cases, it is preferable to stabilize the pH of the culture medium used for culturing fish germline stem cells at around 7-7.5. In such cases, the pH of the medium can be adjusted using known methods. For example, the pH can be adjusted by adding an appropriate amount of buffer such as HEPES to the medium, but this is not the only method.

[0021] In one embodiment, in addition to the components mentioned above, known culture medium additives such as amino acids (essential amino acids, non-essential amino acids, etc.), antibiotics (gentamicin, etc.), minerals (calcium, magnesium, etc.), and buffer solutions (HEPES, etc.) may be added to the culture medium as appropriate.

[0022] The various culture conditions in the method of the present invention are not particularly limited as long as the desired effects of the present invention are obtained. For example, the culture temperature is usually 25 to 39°C (preferably 30 to 37°C). The CO2 concentration is usually 1 to 10% by volume in the culture atmosphere, and preferably 2 to 5% by volume. The culture period can be set as appropriate according to the purpose of the culture, but with the present invention, it may be possible to culture for 1 to 100 days, or even longer than 100 days. The frequency of changing the culture medium may be daily, every 2 days, every 3 days, every 4 days, every 5 days, every 6 days, or every 7 days, but is not limited to these.

[0023] The species of fish to which the method of the present invention can be applied are not particularly limited, but examples include Beloniformes (e.g., medaka, needlefish, saury, etc.), Clupeiformes (e.g., sardines, herring, sprats, etc.), and Perciformes (e.g., wrasse, mackerel, rockfish, etc.). Preferably, medaka, anchovies, starry wrasse, and Pacific mackerel are used, and particularly preferably Pacific mackerel.

[0024] In the method of the present invention, serum may be included, but in a preferred embodiment, the medium used in the present invention can be a serum-free medium. By not using serum, various demerits of using serum (e.g., high cost, problems related to standardization, contamination, etc.) can be avoided, and germline stem cells with relatively low cost and high quality can be stably produced.

[0025] In addition, in one embodiment, the method of the present invention can also be carried out under feeder-free conditions. By culturing germline stem cells under feeder-free conditions, it becomes possible to avoid contamination of feeder cells during the recovery of cultured germline stem cells, which is preferable.

[0026] In one embodiment, the method of the present invention may proliferate a large amount of germline stem cells while maintaining them for a long period by subculturing the germline stem cells. A method known per se can be used for subculture. In one embodiment, it may be preferable to optimize the cell density at the time of subculture. The preferred cell density is usually 0.5×10 5 ~6.5×10 5 cells / cm 2 and more preferably 1×10 5 ~5.0×10 5 cells / cm 2 and even more preferably 2×10 5 ~4.5×10 5 cells / cm 2 but is not limited thereto.

[0027] 2. Kit for culturing fish germline stem cells The present invention also provides a kit for culturing fish germline stem cells (hereinafter sometimes referred to as "the kit of the present invention"), which includes the following: Vitronectin, and the following 8 components: (1) insulin, (2) selenium, (3) transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO3 or KHCO3, (8) L-glutamine.

[0028] In one embodiment, the kit of the present invention may further include a basal medium.

[0029] The basal culture medium, vitronectin, eight specific components, and fish species included in the kit of the present invention are the same as those described in the method of the present invention.

[0030] The vitronectin, eight specific components, and basal culture medium included in the kit of the present invention may be contained within the kit in separate containers. The eight specific components may be contained in individual containers, or two or more components may be contained in a single container. All eight components may also be mixed and contained in a single container.

[0031] In one preferred embodiment, the vitronectin and eight specific components included in the kit of the present invention may be provided in a form dissolved or dispersed in a suitable solution. The basal medium may also be provided in the form of a liquid medium.

[0032] As described in the method of the present invention, NaHCO3 can be substituted with an equal amount of KHCO3. Therefore, in one embodiment, NaHCO3 may be substituted with KHCO3.

[0033] In another embodiment, if the kit of the present invention contains KHCO3, it is preferable to include sodium chloride (NaCl) as an additional component. The kit of the present invention allows the method of the present invention to be carried out easily. Therefore, the kit of the present invention can also be described as a kit for carrying out the method of the present invention.

[0034] The present invention will be described in more detail in the following examples, but the present invention is not limited in any way by these examples. [Examples]

[0035] [Test Example 1] Isolation of germline stem cells The germline stem cells of mackerel and medaka used in the following examples were isolated by known methods. In short, they were isolated by the following procedure.

[0036] The gonads were collected under sterile conditions and incubated in 0.001% tetracycline hydrochloride-containing DPBS (DPBS-AB) for at least 2 hours. The gonads were then washed at least three times with calcium-free DPBS-AB, followed by 2-5 mm of water. 3 The gonads were dissected into small pieces. The tissue was washed with 3 mL of Accumax per gram to remove any remaining DPBS. 12 mL of Accumax per gram of tissue was added, and all contents were transferred to a disposable 10 cm dish. The mixture was incubated at room temperature with occasional stirring using a glass Pasteur pipette until a homogeneous mixture was obtained (at least 2 hours for ovaries and at least 3 hours for testes). The resulting mixture was filtered through a 100 μm pore mesh, and then through 40 μm and 20 μm pore meshes. The filtrate was centrifuged at 1400 g for 30 minutes at room temperature. The cell pellet was washed at least three times with DPBS-BSA, and then once more with the next medium to be used. Finally, the washed cell pellet was dispersed in the next medium at a rate of 1 mL per 0.1 g of pellet. Germ stem cells were then isolated from the dispersed cell population by magnetic separation using rat anti-CD90.2 antibody conjugated with magnetic beads.

[0037] [Test Example 2] Preparation of Culture Medium Eight types of culture media were prepared using DMEM / F12 (Ham) 1:1 medium (hereinafter sometimes simply referred to as DMEM medium) or L15 medium as a base, each containing the components listed in Tables 1 and 2 below.

[0038] [Table 1]

[0039] [Table 2]

[0040] [Example 1] Investigation of culture medium components suitable for culturing fish germline stem cells 1 Mackerel germ stem cells prepared in Test Example 1 were cultured in a vitronectin-coated container using the eight types of culture media prepared in Test Example 2, and the percentage of CD90.2-positive cells after culture was confirmed. CD90.2 positivity indicates the presence of stem cell characteristics. The cell count at the start of culture was 6.5 × 10⁶. 5 1 or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²) 2 ). As a negative control, germline stem cells were cultured in DMEM medium or L15 medium in containers not coated with vitronectin. The cells were cultured in a CO2 incubator (Panasonic) at a culture temperature of 27-33°C and a CO2 concentration of 2-5%. The incubator was humidified with sterile distilled water supplemented with 0.0001% sodium lauryl sulfate (Nakarai). The incubator was UV sterilized for 15 minutes every 4 days and washed with H2O2 every month. CD90.2-positive cells were immunostained using a fluorescently labeled antibody against CD90.2 and analyzed using a cell analyzer (Sony EC800). The results are shown in Figure 1.

[0041] As shown in Figure 1, under conditions without E8 supplements or other additives and without the coating of vitronectin (labeled "1" in Figure 1), few or no CD90.2-positive cells were observed. On the other hand, under conditions where germline stem cells were cultured in containers containing E8 and coated with vitronectin, a large number of CD90.2-positive cells were observed. Furthermore, it was observed that using DMEM as the basal medium tended to yield a larger number of CD90.2-positive cells.

[0042] [Example 2] Investigation of culture medium components suitable for culturing fish germline stem cells 2 Mackerel germ stem cells prepared in Test Example 1 were cultured in a vitronectin-coated container using eight types of culture media (and two types of media for negative control) prepared in Test Example 2, and the stem cell properties and doubling time after culture were confirmed. The cell count at the start of culture was 3.25 × 10⁶. 5 pieces, 6.5×10 5 1 piece, or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²)2 ). As a negative control, germline stem cells were cultured in DMEM medium or L15 medium in a container not coated with vitronectin. Undifferentiated state and doubling time were confirmed after 24 hours of culture. The experiment was performed with n=6. Stem cell properties were calculated using CD90.2 staining, and cell analysis was performed using Sony EC800. All other experimental conditions were the same as those in Example 1. The doubling time was calculated using the following formula after determining the initial cell number (N0) at time t0 and the cell number (N) after time t: Cell population doubling time (CPDT) = (t-t0) / (3.32*(LOG) 10 (N)-LOG 10 (N0))

[0043] The results are shown in Figure 2 (Stem cell characteristics) and Figure 3 (Doubling time). Stem cell characteristics could be maintained regardless of whether DMEM medium or L15 medium was used as the basal medium, as shown in Figure 2. Furthermore, similar to Example 1, stem cell characteristics could be maintained more efficiently when DMEM medium was used as the basal medium.

[0044] As shown in Figure 3, the doubling time tended to be shorter when DMEM was used as the basal medium compared to L15. Furthermore, the doubling time tended to vary depending on the initial number of cells seeded. (Note that negative values ​​indicate a decrease in the number of cells.)

[0045] Based on these results, it was possible to maintain stem cell properties under specific conditions, regardless of whether DMEM medium or L15 medium was used as the basal culture medium, and efficient proliferation of germline stem cells was achieved under those specific conditions.

[0046] [Example 3] Investigation of culture medium components suitable for culturing fish germline stem cells 3 Under the same conditions as in Example 1, except that the basal medium was DMEM only, germline stem cells of Pacific mackerel prepared in Test Example 1 were cultured, and cell viability, confluence, and CFU (Colony Forming Unit) were checked 24 hours after the start of culture. The number of cells at the start of culture was 3.1 × 10⁶. 5 pieces, 6.25×10 5 1 piece, or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²) 2 The study was conducted with n=6. Survival rates were calculated using propidium iodide and Hoechst staining, and cell analysis was performed using a Sony EC800. Confluence was calculated as the ratio of the area covered by cells to the total available area of ​​the culture medium. Colonies (>50 microns) were counted individually. The results are shown in Figure 4.

[0047] As shown in Figure 4, germline stem cells can be cultured in any of the culture medium compositions 2-4 (DMEM) using a container coated with vitronectin. Furthermore, the conditions of culture medium 4 (DMEM) were shown to be particularly preferable.

[0048] [Example 4] Investigation of the optimal cell density during subculturing 1 The optimal cell density during subculturing was investigated using medium 4 (DMEM) from Example 1. The number of cells during subculturing was 3.1 × 10⁶. 5 pieces, 6.25×10 5 pieces, 12.5×10 5 1 piece, or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²) 2The cells were subculturized using the following procedure: Subculturing was performed at 4-day intervals. Between each subculturing, the upper layer of the used culture medium (70-80% of the total medium) that did not contain cells was discarded. The cells were then gently suspended using a pipette. The cell suspension was collected in a 50 ml conical tube and recovered by centrifugation at 1400 × g for 10 minutes. The cell pellet was carefully suspended in fresh final medium. The number of cells was counted and seeded in a container coated with vitronectin. After 46-52 hours of subculturing, the cell number, doubling time, stem cell nature, and viability were calculated. The cell number was calculated using a cell analyzer. The doubling time, stem cell nature, and viability were calculated using the same method as described above. The results are shown in Figure 5 (cell number, doubling time, stem cell nature, viability) and Figure 6 (photographs of the cell populations after culture under each condition after 96 hours of subculturing).

[0049] As shown in Figures 5 and 6, it was demonstrated that efficient subculturing is possible by keeping the cell density relatively low during subculturing.

[0050] [Example 5] Detection of cell proliferation rate and cell markers after proliferation Mackerel germline stem cells prepared in Test Example 1 were cultured in a vianectin-coated container in DMEM / F12 (Ham) 1:1 medium containing insulin (19.4 mg / L), selenium (14 μg / L), transferrin (10.7 mg / L), L-ascorbic acid (64 mg / L), FGF2 (200 μg / L), TGFβ (2 μg / L), NaHCO3 (1.743 g / L), L-glutamine (100 mg / L), and HEPES (15 mM). The cell proliferation rate and the expression status of cell markers (CD90.2, KLF, OCT4, GFR1a, and VASA) were confirmed. Cell markers were identified using live cell immunohistochemistry. Cells were passaged every 4 days. The results are shown in Figure 7 (cell number), Figure 8 (expression of cell markers), and Table 3 (expression levels of cell markers).

[0051] [Table 3]

[0052] As shown in Figure 7, the cell number of both female and male germ stem cells increased over time. Furthermore, as shown in Figure 8, the cultured germ stem cells expressed cellular markers such as CD90.2, KLF4, OCT4, GFR1a, and VASA. In addition, as shown in Table 3, these expression markers were still expressed after 25 passages (100 days).

[0053] [Example 6] Investigation of culture medium components suitable for culturing fish germline stem cells 4 We investigated conditions that enable the maintenance and expansion culture of fish germline stem cells. Medaka germline stem cells prepared in Test Example 1 were used. DMEM / F12 (Ham) 1:1 medium was used as the basal medium. Serum (10%), KSR (KnockOut TM The presence or absence of the following substances was investigated: Serum Replacement) Thermo Fisher Scientific (GIBCO)), mackerel plasma (1%, the plasma was prepared as follows: mackerel blood was collected by cardiac puncture using a 23-gauge needle and syringe treated with 0.25% EDTA disodium, and the blood was immediately centrifuged at 6000 rpm for 10 minutes to collect the supernatant. The plasma was irradiated with UV for 5 minutes before use and filtered using a 0.22 micron filter. The plasma used in this example was prepared by mixing plasma collected from mackerel of various ages and sexes.), vitronectin (human-derived, Thermo Fisher Scientific (GIBCO)), and eight specific components (substituted with E8 supplement; insulin, etc., are recombinant peptides of human origin). The culture conditions were the same as in Example 1. The results are shown in Figure 9.

[0054] As shown in Figure 9, germline stem cells can be cultured in a culture medium containing the E8 supplement in a viaronectin-coated container, and serum and plasma are not necessarily required. In other words, fish germline stem cells can be cultured in a viaronectin-coated container using a basal culture medium containing (1) insulin, (2) selenium, (3) transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO3, and (8) L-glutamine.

[0055] [Example 7] Investigation of culture medium components suitable for culturing fish germline stem cells 5 The germline stem cells of Pacific mackerel prepared in Test Example 1 were cultured under various culture conditions 1 to 5 shown in Figure 10, and the percentage of CD90.2-positive cells after culture was confirmed. The cell count at the start of culture was 6.5 × 10⁶. 5 1 or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²) 2 The same conditions as in Example 1 were used for culture temperature, CO2 concentration, and other factors. The culture medium used in this example is as follows: DMEM-NAHCO3 (DMEM containing 1.743 g / L of NaHCO3 (see Table 1 for components other than DMEM)) DMEM-KHCO3 (DMEM containing 1.743 g / L of KHCO3 (see Table 1 for components other than DMEM)) L15-NAHCO3 (L15 containing 1.743 g / L of NaHCO3 (see Table 2 for components other than L15))

[0056] The results are shown in Figure 10. As shown in Figure 10, it was demonstrated that NaHCO3 can be substituted for KHCO3 in the culture of fish germline stem cells.

[0057] [Example 8] Investigation of the optimal cell density during subculturing 2 In the culture conditions of Example 7, we investigated whether the cell density during subculturing affected stem cell characteristics and doubling time. Mackerel germ stem cells prepared in Test Example 1 were used. The cell count during subculturing was 3.1 × 10⁶. 5 pieces, 6.25×10 5 pieces, 12.5×10 5 1 piece, or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²) 2 The stem cell properties and doubling time were determined in the same manner as in Example 4. The results are shown in Figure 11.

[0058] As shown in Figure 11, DMEM-NAHCO3 and DMEM-KHCO3 showed similar trends in terms of stem cell characteristics and doubling time, regardless of cell density during passage.

[0059] [Example 9] Investigation of culture medium components suitable for culturing fish germline stem cells 6 In the two culture media (DMEM-NAHCO3 and DMEM-KHCO3) prepared in Example 7, germline stem cells of Pacific mackerel prepared in Test Example 1 were seeded at three different cell densities, and viability, confluency, and CFU (Colony forming Unit) at 24 hours were determined using the same method as in Example 3. Each experiment was conducted with N=6. The results are shown in Figure 12.

[0060] As shown in Figure 12, although there may be slight differences in trends due to differences in cell density at seeding, both DMEM-NAHCO3 and DMEM-KHCO3 were shown to be suitable for culturing fish germline stem cells in terms of viability, confluence, and CFU. The culture medium "4" (see Table 1 for detailed components), which yielded the most favorable results from Examples 7-9, will hereafter be referred to as "Media C" and "Media N". Specifically, "Media C" and "Media N" are as follows: Media C: DMEM / F12(ham) 1:1 + E8 supplement (except NaHCO3) + NaHCO3 (1.743 g / L) + L-ascorbic acid (64 mg / L) added (total 128 mg / L) Media N: DMEM / F12(ham) 1:1 + E8 supplement (excluding NaHCO3) + KHCO3 (1.743 g / L) + L-ascorbic acid (64 mg / L) added (total 128 mg / L)

[0061] [Example 10] Investigation of culture medium components suitable for culturing fish germline stem cells 7 Germ stem cells from medaka and mackerel prepared in Test Example 1 were cultured under various culture conditions shown in Figure 13, and their stem cell properties and viability were determined after 96 hours. In Figure 13, "Medium" refers to DMEM, and Serum, Plasma, and Vitronectin are the same as those used in Example 6. The results are shown in Figure 13.

[0062] As shown in Figure 13, the stem cell properties and viability of germline stem cells from medaka and mackerel were shown to be better when cultured in a container coated with vitronectin and using Media C or Media N.

[0063] [Example 11] Investigation of the optimal cell density during subculturing 3 The optimal cell density for culturing mackerel germline stem cells prepared in Test Example 1 using a vitronectin-coated container and Media C was investigated. The cell density was 3.1 × 10⁶. 5 pieces, 6.25×10 5 pieces, 12.5×10 5 1 piece, or 25 x 10 5 (The area of ​​the culture dish used was 1.9 cm²) 2 The cells were seeded using [a specific method]. Cell number, doubling time, confluence, stem cell characteristics, and viability were determined at 24, 48, 72, and 96 hours after culturing. The results are shown in Figures 14 and 15.

[0064] As shown in Figure 14, 12.5 × 10⁻⁵ units / 1.9 cm 2 When seeding was performed at the above cell densities, stem cell characteristics and survival rates decreased. Furthermore, as shown in Figure 15, 12.5 × 10⁻¹ cells / 1.9 cm² 2 When seeding was performed at the above cell densities, aggregates were observed in some parts of the cell population. Therefore, it was shown that a relatively low cell density is preferable during subculturing.

[0065] [Example 12] Investigation of the optimal cell density during subculturing 4 The optimal cell density of germline stem cells from Pacific mackerel was investigated using the same conditions as in Example 11, except that the culture medium used was changed to Media N. Cell number, doubling time, stem cell characteristics, and viability were determined at 24, 48, 72, and 96 hours after culturing. The results are shown in Figure 16.

[0066] As shown in Figure 16, 12.5 × 10⁻⁵ units / 1.9 cm 2 When seeding was performed at the above cell densities, stem cell characteristics and survival rates decreased. Interestingly, the effect of cell density on stem cell characteristics and survival rates was shown to be greater in Medium N than in Medium C.

[0067] [Example 13] Improvement of DMEM-KHCO3 medium As shown in Example 12, Medium N (a medium to which ascorbic acid has been added to DMEM-KHCO3) is less tolerant of cell density than Medium C (a medium to which ascorbic acid has been added to DMEM-NAHCO3). Furthermore, when culturing fish germline stem cells using DMEM-KHCO3 in the above experiment, the cells tended to detach easily from the surface of the culture vessel after about two weeks. Therefore, improvements to DMEM-KHCO3 were considered.

[0068] Medium N uses DMEM / F12 as its base medium and also contains insulin, selenium, transferrin, L-ascorbic acid, FGF2, TGFβ, L-glutamine, KHCO3, and HEPES (and also contains gentamicin as an antibiotic). The inventors added various test substances to Medium N and selected substances suitable for improving Medium N. The selection criteria used were stem cell characteristics, viability, mortality, confluence (after 2 days), and colony count (after 4 days). Germ stem cells from Pacific mackerel were used. The test period was 15 days. The test consisted of N=6. Stem cell characteristics, viability, mortality, confluence, and colony count were calculated using the results from Media C as a baseline.

[0069] The selection results showed that adding NaCl could significantly improve Medium N. The results with added NaCl are shown in Figure 17. In Figure 17, "FSC10" refers to a medium prepared by adding 60.9 ug / L of sodium selenite (Na2SeO3) (equivalent to 21 ug / L of selenium) and 121 mg / L of NaCl to Medium N. E8 refers to E8 medium (DMEM / F12 (Ham) (1:1) (pH 7.4) containing insulin 19.4 mg / L, selenium 14 ug / L, transferrin 10.7 mg / L, L-ascorbic acid 64 mg / L, FGF2 100 ug / L, TGFβ- 2 ug / L, L-glutamine 100 mg / L, NAHCO3 1.743 g / L, and HEPES 15 mM).

[0070] As shown in Figure 17, FSC10 showed better results compared to Media N in terms of stem cell characteristics, survival rate, mortality rate, confluence, and colony number.

[0071] [Example 14] Investigation of the concentration range of components contained in FSC10 medium The preferred concentration range for the components of FSC10 was investigated. Germ stem cells from medaka and mackerel were used. The test period was 7 days. The test consisted of N=10. Stem cell properties, viability, confluence, and CFU were used as criteria. Compared with the FSC10 prepared in Example 13, concentrations were determined in a range where each criterion was at least 70% or higher. The results are shown in Figure 18. [Industrial applicability]

[0072] According to the present invention, fish germ cells of stable quality can be efficiently proliferated at a relatively low cost. Therefore, the present invention is extremely useful in fields such as experimental research on fish, as well as in fish production and breeding.

Claims

1. A method for culturing fish germline stem cells, comprising culturing fish germline stem cells on a surface coated with vitronectin in a culture medium containing the following eight components, wherein the basal medium in the culture medium is DMEM / F12(Ham) medium: (1) Insulin, (2) Selenium, (3) Transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO 3 or KHCO 3 , (8) L-glutamine.

2. The method according to claim 1, wherein (7) is KHCO3.

3. The method according to claim 2, wherein the culture medium further comprises sodium chloride.

4. The method according to any one of claims 1 to 3, wherein the culture medium is a serum-free medium.

5. The method according to any one of claims 1 to 4, carried out under feeder-free conditions.

6. 0.5 × 10 during subgeneration 5 ~6.5 x 10 5 cells / cm 2 The method according to any one of claims 1 to 5, further comprising the step of resowing.

7. A kit for culturing fish germline stem cells, including the following: Vitronectin, The following 8 components: (1) Insulin, (2) Selenium, (3) Transferrin, (4) L-ascorbic acid, (5) FGF2, (6) TGFβ, (7) NaHCO 3 or KHCO 3 , (8) L-glutamine, and DMEM / F12 (Ham) medium.

8. The kit according to claim 7, wherein (7) is KHCO3.

9. The kit according to claim 8, further comprising sodium chloride.

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