A culture medium and its application and method for inducing tendon stem cells to differentiate into fat cells
A technology of adipocyte differentiation and tendon stem cells, applied in the field of stem cell culture, can solve the problems that the differentiation mechanism of tendon stem cells has not been clearly studied
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Embodiment 1
[0034] Human Achilles tendon tissue was collected under sterile conditions, rinsed with PBS three times, part of the connective tissue on the surface was cut off, and the Achilles tendon tissue was separated. The Achilles tendon was cut into pieces of 1mm×1mm×1mm, digested with 3mg / mL type Ⅰ collagenase at 37°C for 2h, and filtered through a 70μm filter to form a single cell suspension. Centrifuge the single cell suspension at 300×g for 5 min, discard the supernatant, and resuspend the cell pellet in complete medium (L-DMEM medium containing 10% FBS, 100 U / mL penicillin, 100 mg / mL streptomycin) , at 500 pieces / cm 2 The cell density was seeded into a 10cm-diameter petri dish, cultured for 10 days, digested with 0.25% trypsin, mixed, and labeled as primary cells. Subculture after the cells cover 90% of the bottom of the bottle, discard the culture medium, wash twice with sterile PBS, digest with 0.25% trypsin for 3 minutes, add complete medium to stop digestion; centrifuge the ...
Embodiment 2
[0038] Adipogenic induction: Take the 3rd passage cells and use 5×10 4 The cells / well density were inoculated in 6-well plates, and the experiments were divided into the following groups:
[0039] The blank control group continued to be cultured with L-DMEM containing 10% FBS.
[0040] The positive control group was cultured in the culture medium of L-DMEM containing 10% FBS, 500nmol / L dexamethasone, 500 μmol / L isobutylmethylxanthine, 50 μmol / L indomethacin, and 10 μg / mL insulin;
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