A method for inducing chondrogenic differentiation of stem cells
A technology of stem cells and cartilage, applied in biochemical equipment and methods, animal cells, vertebrate cells, etc., can solve problems such as decomposition, high price, and influence on characteristics, achieve good cartilage differentiation ability, prevent protease decomposition, and help effect on secretion
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Embodiment 1
[0033] Example 1 Transfection of adenovirus carrying TGF-β3 into chondrocytes
[0034] (1) Construct an adenoviral vector carrying transforming growth factor TGF-β3,
[0035] Purchase the Adeno-XTM ViraTrakTM ZsGreen1 Expression System 2 kit, add Xhol / NotI recognition sites at both ends of the transforming growth factor TGF-β3 sequence by PCR, and then use DNA recombination technology to insert the TGF-β3 sequence into the adenovirus vector ( Green fluorescent protein adenoviral vector), construct an adenoviral vector (Ad-T3) carrying TGF-β3, Ad-T3 amplified to >10 9IFU / mL and then frozen for later use. The specific construction method refers to the following literature: Hao, J. H., Yao, Y. C., Varshney, R. R., Wang, L. C., Prakash, C., Li, H., Wang, D. A., Gene Transfer and Living Release of Transforming Growth Factor-Beta 3 for Cartilage Tissue Engineering Applications, Tissue Engineering Part C Methods, 14 (2008), 4: 273-280.
[0036] (2) Isolation and culture of chondro...
Embodiment 2
[0039] Example 2 Observation of the culture process of ATDC5 cells and transfected chondrocyte co-culture system (named 3A1C) and detection of directional cartilage differentiation
[0040] (1) Purchase ATDC5 cells from Abgent (San Diego) (this cell is recognized as a substitute for stem cells as model cells), using F12 medium [containing 0.5% FBS (fetal bovine serum) and 1% penicillin-streptomycin penicillin-streptomycin (Double Antibody)] Passage ATDC5 cells to 3 passages and freeze them for later use;
[0041] (2) ATDC5 cells and transfected chondrocytes were digested, collected, counted, mixed at a ratio of 3:1, and 1.2% sodium alginate solution was added to prepare a cell density of 6×10 6 cells / mL of cell suspension. Take 50uL of the above cell suspension with a special pipette tip, and quickly inject it into 102mM CaCl 2 solution to form a cell gel (results image 3 ), and after 10 min, remove the cell gel with a long spoon and place it on a 24-well plate, one capsul...
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