A method for isolating and culturing esophageal epithelial stem cells
A technology for separating and culturing stem cells, applied in the field of cell biology, which can solve the problems of unresearched methods of separating and culturing esophageal epithelial stem cells, and achieve the effects of prolonging cell activity, inhibiting multi-directional differentiation potential, and stabilizing heredity
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Embodiment 1
[0029] Isolation, culture and identification of human esophageal epithelial stem cells
[0030] 1.1 Isolation and culture
[0031] (1) Materials: The discarded normal esophageal epithelial tissue of a 69-year-old male was removed under aseptic conditions, and placed in phosphate-buffered saline (PBS) / physiological in a sterile tube of saline solution and bring it back to the laboratory immediately;
[0032] (2) Separation: Wash the esophageal epithelial tissue 3 to 5 times with PBS containing 200 μg / mL penicillin / streptomycin, and remove hemorrhagic tissue, necrotic tissue and fibrovascular tissue; Scissors and ophthalmic forceps to trim the tissue to 0.5-1mm 3 Then add the centrifuge tube containing the digestion solution of 0.1% collagenase type I, 0.1% pronase and 0.5mg / ml deoxyribonuclease I, and then put the centrifuge tube into a 37°C incubator for constant temperature digestion for 2h Afterwards, the digestion mixture was filtered through a 200-mesh cell sieve and ce...
Embodiment 2
[0052] Isolation, culture and identification of mouse esophageal epithelial stem cells
[0053] 1. Cell isolation and culture
[0054] All animal studies were performed in full compliance with laboratory-grade animal standards. The normal esophageal tissues were taken out from the mice and washed three times with PBS containing antibiotics. Under sterile conditions, use sterile ophthalmic scissors and ophthalmic forceps to remove the hemorrhage and necrotic tissue in the esophagus, and cut them into pieces of 0.5-1mm 3 and then added to a centrifuge tube containing a digestion solution of 0.1% pronase and 0.5 mg / ml DNase I. Digest at a constant temperature of 37°C for 3 hours, filter and centrifuge, and collect the cell pellet.
[0055] Resuspend the cells with the culture medium and place them in the culture flask / dish covered with the coating solution for horizontal culture. The culture solution was coated for 2 hours, the culture solution was discarded, and washed 5 tim...
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