Preparation method and application of adipose-derived mesenchymal stem cells and preparation thereof
A technology of mesenchymal stem cells and stem cells, which is applied in the field of preparation of adipose-derived mesenchymal stem cells and their preparations, can solve the problems of limitations and low purity, and achieve the effects of accelerating regeneration and replacement, high purity, and promoting proliferation
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Embodiment 1
[0051] Example 1 Adipose-derived mesenchymal stem cell extraction
[0052] 1. Obtain the fat solution and transfer it to a laboratory ultra-clean bench at 4°C;
[0053] 2. Divide adipose tissue evenly into 50mL centrifuge tubes, add 0.5% type I collagenase to each tube, seal and shake back and forth horizontally to mix well. The volume ratio of the type I collagenase to the fat is 0.5-1:1.
[0054] 3. Transfer to a constant temperature air shaker, digest at 37°C and 100R for 50 minutes; add 1mL FBS with a 1mL pipette tip to stop the digestion, blow evenly with a Pasteur pipette, balance the centrifuge tube, put it in a centrifuge, and centrifuge at 1500rpm / min for 5min .
[0055] 4. Aspirate the supernatant with a Pasteur pipette, add 40mL PBS to each tube to resuspend the cells, take 20uL of the cell suspension and count it with a cell counter, balance the centrifuge tubes, place them in a centrifuge, and centrifuge at 1500rpm / min for 5min.
[0056] 5. Use a Pasteur pipett...
Embodiment 2
[0058] Example 2 Flow cytometric identification of adipose-derived mesenchymal stem cells
[0059] Such as figure 2 As shown, from the results of flow cytometry, the surface markers of adipose-derived mesenchymal stem cells
[0060] CD59+CD90+CD45-HLA-DR- up to 99.7%.
Embodiment 3
[0061] Example 3 Adipose-derived mesenchymal stem cell culture
[0062] After 1.48 hours, use a Pasteur pipette to suck off the medium in the dish prepared in Example 1, add 10 mL of PBS to each dish for washing, and repeat twice.
[0063] 2. Inoculate 10mL of cell suspension into a 10cm culture dish, and add 100uL of 1ug / mL EGF to each dish. Shake the culture dish 5 times to make the cell suspension evenly distributed in the culture dish, transfer to 5% CO 2 , 37°C, and a cell incubator with a saturated humidity of 95% to continue culturing, observe the state of the cells and take pictures every day.
[0064] 3. When the cells grow to 80% confluence, discard the culture medium, add 10ml of PBS to wash once, add 4ml of 0.25w / v% EDTA-trypsin solution to digest for 1-2min. The concentration of EDTA-trypsin in the EDTA-trypsin solution is 0.25w / v%, and the ratio of the adherent area of the adipose-derived mesenchymal stem cells to the EDTA-trypsin solution is: every 10cm 2 A...
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