Application of miRNA in preparation of medicine for preventing and treating osteoarthritis, exosome with high expression of miRNA, and application of exosome
A technology for osteoarthritis and exosomes, which is applied in the field of miRNA and exosomes, can solve problems such as unimproved joint damage, achieve the effects of promoting chondrocyte proliferation, promoting cartilage regeneration, and reducing osteoarthritis damage
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[0028] In the present invention, the preparation method of the SMSC-155-5p-Exos is a conventional preparation method, preferably comprising: extracting synovial tissue from the knee articular cartilage of a patient undergoing total knee arthroplasty for osteoarthritis (Osteoarthritis, OA), Remove fat and some connective tissues, cut them into pieces, add DMEM medium containing collagenase Ⅱ and 20% fetal bovine serum (FBS), and digest overnight in a CO2 incubator; suspend and inoculate the cell pellet on a 60mm culture dish, and change the medium after 24 hours Remove non-adherent cells. Change the medium every 3 days. When the cells grew to 80% confluence, the cells were placed in a medium containing 10% fetal bovine serum (FBS), 25 μg / ml ascorbic acid 2-phosphate and 1% penicillin streptomycin at 37 °C and 5% carbon dioxide. cultured in DMEM medium to obtain synovial mesenchymal stem cells (SMSCs). use 2000 transfection reagent cultured SMSCs at a concentration of 100nM ...
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[0033] The cartilage tissue was extracted from the knee articular cartilage of patients undergoing total knee arthroplasty for osteoarthritis, and the cartilage tissue was extracted with collagenase II to obtain primary chondrocytes. OA chondrocytes were obtained by culturing in DMEM medium containing 10% fetal bovine serum (FBS), 25 μg / ml ascorbic acid 2-phosphate and 1% penicillin-streptomycin. use 2000 transfection reagent was used to culture OA chondrocytes at a concentration of 100 nM and transfect miR-155-5p mimics to obtain transfected chondrocytes. SMSCs were transfected with miR-155-5p mimics, and then separated and concentrated to obtain SMSC-155-5p-Exos.
[0034] The method of separation and concentration is as follows: the transfected chondrocytes are cultivated with serum-free DMEM medium to obtain a culture supernatant; the first supernatant is obtained after the culture supernatant is subjected to the first centrifugation (centrifugal force is 1000r / min). Sup...
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