Pelodiscus sinensis heart cell continuous cell line and establishing method and ultra-low-temperature cryopreservation method thereof
A heart cell and construction method technology, applied in artificial cell constructs, animal cells, vertebrate cells, etc., can solve problems such as restricting in-depth research on Chinese soft-shelled turtle virus diseases, and achieve the effect of avoiding the difficulty of cell migration.
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Embodiment 1
[0028] Example 1: Construction of a continuous cell line of soft-shelled turtle heart cells
[0029] 1.1 Preparation of PBS disinfectant and cell culture medium
[0030] PBS disinfectant solution: Add antibiotics to PBS so that the penicillin concentration is 100 IU / ml, the streptomycin concentration is 100 μg / ml, and the amphotericin B concentration is 20 μg / ml.
[0031] Primary culture medium: add fetal bovine serum, cell growth factor EGF and antibiotics to the MEM medium, so that the volume of fetal bovine serum accounts for 15% of the total volume, the concentration of EGF is 10ng / ml, the concentration of penicillin is 100IU / ml, streptomycin The concentration of acetaminophen was 100 μg / ml, the concentration of amphotericin B was 20 μg / ml, the pH value of the culture medium was adjusted to 7.0-7.2, and it was stored in a 4-degree refrigerator for later use.
[0032] Subculture medium: add fetal bovine serum and antibiotics to the MEM medium, so that the volume of fetal b...
Embodiment 2
[0037] Example 2: Construction of a continuous cell line of soft-shelled turtle heart cells
[0038] 2.1 Primary culture
[0039] Use 0.1% potassium permanganate solution to soak and disinfect the soft-shelled turtle body for 30 minutes. After cleaning, wipe the surface of the soft-shelled turtle body with 75% alcohol, and place it in an ultra-clean workbench. The heart was taken with sterile dissecting instruments, placed in a sterile petri dish, and washed with PBS disinfectant to remove blood clot tissue and connective tissue. Next, cut the heart to 0.8mm with sterile instruments 3 Small and large tissue pieces were digested with 0.125% trypsin at room temperature for 25min, and then the digested tissue pieces were inoculated on 25cm 2 Add 2ml of the primary culture medium to the cell culture flask and place it upside down in a 30°C incubator to start the primary culture. After 24 hours, turn the cell culture flask over and add the primary culture medium to 10ml. Thereaf...
Embodiment 3
[0042] Example 3: Cell cryopreservation and recovery
[0043] 3.1 Cell cryopreservation
[0044] Mix fetal calf serum and DMSO at a volume ratio of 9:1, and mix well to obtain a cell cryopreservation protection solution. Take the cells in the logarithmic growth phase, digest them with 0.25% trypsin-EDTA solution, centrifuge the cell suspension at 1000rpm for 8min, discard the supernatant, add the prepared cell freezing solution to the cell pellet, resuspend, and make the cells The concentration is 1×10 6 cells / ml, transfer 1ml of the cell suspension to a 1.8ml cryopreservation tube and place the cryopreservation tube in a programmed cooling box, overnight at -80°C, and then store it in liquid nitrogen for long-term storage.
[0046] Take the frozen tube out of the liquid nitrogen, put it into a 37°C water bath and shake it quickly until it melts, then transfer the thawed cells to a 15ml centrifuge tube in a sterile operating table, and add an equa...
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