A kind of cultivation method of naked mole rat cardiomyocytes
A technique of cardiomyocytes and a culturing method is applied in the field of culturing naked mole rat cardiomyocytes, which can solve the problem that naked mole rat cardiomyocytes have not been reported, and achieve simple and easy purification operation steps, short time-consuming and high survival rate. Effect
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Embodiment 1
[0046] (1) Add 6 ml of 0.08% trypsin to 10 newborn naked mole rat myocardial tissue blocks at 1-2 days old, place at 35°C, 5% CO 2 After digesting in the cell culture incubator for 6 minutes, discard the supernatant, repeat the above operation and digest again;
[0047] (2) Add 6ml of mixed digestive solution (final concentration of trypsin is 0.08%, final concentration of type II collagenase is 0.1%) to the cell pellet obtained from the above operation, gently pipette the suspension of myocardial tissue, and place it at 35°C in O 2 The volume concentration is 5%, CO 2 Digest for 6 minutes in a cell culture incubator with a volume concentration of 5%, and let stand;
[0048] (3) Collect the supernatant in step (2), filter it with a 200-mesh cell sieve, immediately add an equal amount of stop solution (DMEM low-glucose medium containing 10% FBS) to stop the digestion, and place it in a refrigerated centrifuge at 4°C , 1000rpm, and centrifuge for 5 minutes, the resulting cell ...
Embodiment 2
[0053] (1) Add 6.5 ml of 0.08% trypsin to 12 newborn naked mole rat myocardial tissue pieces at the age of 1-3 days, place at 35°C, O 2 The volume concentration is 5%, CO 2 After digesting for 7 minutes in a cell culture incubator with a volume concentration of 5%, discard the supernatant, repeat the above operation and digest again;
[0054] (2) Add 6.5ml of mixed digestive solution (final concentration of trypsin is 0.08%, final concentration of type II collagenase is 0.1%) to the cell pellet obtained from the above operation, gently pipette the myocardial tissue suspension, and place at 35°C, o 2 The volume concentration is 5%, CO 2 Digest for 7 minutes in a cell culture incubator with a volume concentration of 5%, and let stand;
[0055] (3) Collect the supernatant in step (2), filter it with a 200-mesh cell sieve, immediately add an equal amount of stop solution (DMEM low-glucose medium containing 10% FBS) to stop the digestion, and place it in a refrigerated centrifug...
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