A two-step method to establish an osteoarthritis-like cell model after chondrogenic differentiation of mesenchymal stem cells
An osteoarthritis and cell model technology, applied in biochemical equipment and methods, animal cells, vertebrate cells, etc., to achieve the effect of no species difference, less medical ethics, and easy access
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[0038] Human umbilical cord mesenchymal stem cells (Wharton`s Jelly-derived mesenchymal stem cells, WJ-MSCs) under high concentration of cortisol treatment have poor cartilage-oriented differentiation and susceptibility to osteoarthritis.
[0039] One-step and two-step method to establish osteoarthritis-susceptible cell model after cartilage-directed differentiation of WJ-MSCs ( figure 1 )
[0040] 1. Establishment of three-dimensional directed differentiation model of WJ-MSCs sodium alginate microspheres chondrocytes
[0041] Weigh 160 mg of alginate sodium alginate (Sigma, low-viscosity type), put it into a transparent and clean glass bottle with a volume greater than 20 mL, then add 10 mL of double-distilled water to the sterile operating table, and put a magnetic stirrer in the bottle; seal it, Mix well, and stir overnight with magnetic force until it turns into a uniform and transparent colloidal solution, and then sterilize in a pressure steam sterilizer at 120° C. for ...
example 2
[0093] Changes in mRNA expression of TGFβR1, TGFβR2 and downstream phenotype genes in normal control group and IUGR group neonatal umbilical cord mesenchymal stem cells (Wharton`s jelly-derived mesenchymal stem cells, WJ-MSCs).
[0094] 1. Umbilical cord mesenchymal stem cell culture for total RNA extraction
[0095] Neonatal umbilical cord specimens were collected from the Department of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University. Divided into two groups: normal control group and IUGR group (n≧8), total RNA was extracted after culturing mesenchymal stem cells.
[0096] Add 1ml Trizol to the homogenizer, after fully homogenized on ice, transfer to RNase-free 1.5ml EP tube; add 200μl chloroform for extraction, shake vigorously for 15s, let stand on ice for 10min; centrifuge at 12,000×rpm at 4°C for 15min; Carefully pipette 500 μl of the upper aqueous phase into a new RNase-free 1.5ml EP tube, add an equal volume of isopropanol, invert and mix to precipitat...
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