A method for promoting the proliferation of human bone marrow mesenchymal stem cells based on exosomes
A technology of bone marrow mesenchymal stem cells, applied in the field of promoting the growth of human bone marrow mesenchymal stem cells, can solve different problems and achieve the effect of stable properties
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Embodiment 1
[0038] Example 1: Separation and purification of umbilical cord mesenchymal stem cells
[0039] The main materials and sources used are as follows:
[0040] Reagents: low-sugar DMEM (product of Gibco), mesenchymal stem cell medium (product of Dako), trypsin (product of Gibco), BCA protein quantification kit (Beyond), 5XSDS loading buffer, CD63 Rabbit anti-human antibody (BD pharmingen), CD9 rabbit anti-human antibody (BD pharmingen), HRP-labeled goat anti-rabbit IgG secondary antibody (Tiangen company), ECL chemiluminescent detection kit (Beiyuntian company).
[0041] Instruments: inverted microscope (Olympus), carbon dioxide incubator (Thermo), purification bench, desktop centrifuge, transmission electron microscope (Philips), chemiluminescence gel imaging system (bioshine).
[0042] The umbilical cord was obtained from the Obstetrics and Gynecology Department of Changhai Hospital.
[0043] 1. Culture of human umbilical cord mesenchymal stem cells:
[0044] After harvestin...
Embodiment 2
[0052] Embodiment 2: cell proliferation experiment
[0053] 1. Cell count
[0054] Human bone marrow mesenchymal stem cells (bone marrow primary culture, bone marrow from the Department of Orthopedics, Changzheng Hospital, preparation method reference: Majumdar, M.K., Banks, V., Peluso, D.P., and Morris, E.A. (2000) Isolation, characterization, and chondrogenic potential of human bone marrow-derived multipotential stromal cells. Journal of cellular physiology. 185, 98-106) were inoculated into 96-well plates at a concentration of 1000 cells per well, and then added human umbilical cord mesenchymal stem cells after quantitative protein concentration Secretosomes were added according to the final concentration of 10 μg / ml and 20 μg / ml in the culture medium respectively, which were set as 10 μg / ml group and 20 μg / ml group, and a blank control group was set at the same time, set at 6h, 12h, and 24h , 36h four counting time points, set three wells for each time point in each group...
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