Cell culture method for improving hepatocyte proliferation activity
A technology of proliferation activity and cell culture, which is applied in the field of cell culture to improve the proliferation activity of hepatocytes, can solve the problems of large differences in the real structure of the liver, and achieve the effect of good function and activity, and maintenance of function and activity.
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Embodiment 1
[0031] Hepatocytes (LO2 cell line, purchased from the Cell Resource Center, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences) were cultured in complete medium to 80%-90% confluence, removed the complete medium, washed once with 0.01 MPBS, and washed once with 0.25% pancreatic Enzyme digestion for 2 minutes; add an equal volume to stop, after centrifuging at 300g for 5 minutes, collect the cells and add co-cultivation medium to adjust the cell solubility to 2.8×10 6 individual / mL.
Embodiment 2
[0033] Vascular endothelial cells (HUVECs, Basic Medical Cell Center, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences) were cultured in complete medium until they reached 80%-90% confluence, removed the complete medium, washed once with 0.01MPBS, and digested with 0.25% trypsin 2 minutes; add an equal volume of complete medium to stop, after centrifuging at 300g for 5 minutes, collect the cells and add co-cultivation medium to adjust the cell solubility to 0.6×10 6 individual / mL.
Embodiment 3
[0035] Human adipose stem cells (Kunming Cell Bank, Type Culture Collection Committee, Chinese Academy of Sciences) were cultured in complete medium to 80%-90% confluence, removed the complete medium, washed once with 0.01MPBS, and digested with 0.25% trypsin for 2 minutes; Add an equal volume of complete medium to stop, after centrifuging at 300g for 5 minutes, collect the cells and add co-cultivation medium to adjust the cell solubility to 0.6×10 6 individual / mL.
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