Application of Kartogenin (KGN) to preparation of drugs for improving osteogenic differentiation capability of bone marrow mesenchymal stem cells (BM-MSCs)
A technology of bone marrow mesenchymal and osteogenic differentiation, applied in the field of cell medicine, can solve the problem of no related reports on KGN osteogenic induction, and achieve the effect of delaying the process of osteoporosis, promoting osteogenic differentiation and promoting bone healing.
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Embodiment 1
[0033] (1) Resuscitated bone marrow mesenchymal stem cells, inoculated at 175cm 2 Add 20 mL of complete medium to the culture flask, place at 37°C, 5% CO 2 Incubate in the incubator and change the medium every three days. Cells in the logarithmic growth phase were inoculated in multiple 12-well culture plates, complete medium was added, and the medium was changed every three days. After the cell density was greater than 90%, they were divided into groups, and osteogenic induction medium was added. At the same time, complete medium (CTRL group), 0.005% DMSO, 10nM KGN, 100nM KGN, and 1000nM KGN were added, and the medium was changed every three days. Alizarin red staining and quantification of calcium nodules were performed 14 days later.
Embodiment 2
[0035] (1) Resuscitated bone marrow mesenchymal stem cells, inoculated at 175cm 2 Add 20 mL of complete medium to the culture flask, place at 37°C, 5% CO 2 Incubate in the incubator and change the medium every three days. Cells in the logarithmic growth phase were inoculated in multiple 12-well culture plates, complete medium was added, and the medium was changed every three days. After the cell density was greater than 90%, they were divided into groups, and osteogenic induction medium was added. At the same time, complete medium (CTRL group), 0.005% DMSO, 10nM KGN, 100nM KGN, and 1000nM KGN were added, and the medium was changed every three days. After 14 days, the expression of osteogenesis-related genes and proteins was detected.
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