2020
DOI: 10.1097/scs.0000000000006748
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Co-Culture of Adipose-Derived Stem Cells and Chondrocytes With Transforming Growth Factor-Beta 3 Promotes Chondrogenic Differentiation

Abstract: Tissue engineering cartilage is a promising strategy to reconstruct the craniofacial cartilaginous defects. It demands plenty of chondrocytes to generate human-sized craniofacial frameworks. Partly replacement of chondrocytes by adipose-derived stem cells (ADSCs) can be an alternative strategy. The study aimed at evaluating the chondrogenic outcome of ADSCs and chondrocytes in direct co-culture with transforming growth factor-beta (TGF-β3). Porcine ADSCs and chondrocytes were obtained from abdomina… Show more

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Cited by 8 publications
(9 citation statements)
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“…Thus, mature cells can induce differentiation of the surrounding undifferentiated cells. 40,41 This could be explained by the small distance of molecular diffusion and the high concentration of cytokines that induce cell differentiation from mature cells and reach undifferentiated cells.…”
Section: Resultsmentioning
confidence: 99%
“…Thus, mature cells can induce differentiation of the surrounding undifferentiated cells. 40,41 This could be explained by the small distance of molecular diffusion and the high concentration of cytokines that induce cell differentiation from mature cells and reach undifferentiated cells.…”
Section: Resultsmentioning
confidence: 99%
“… 104 In addition, cell proliferation was promoted when chondrocytes were cocultured with adipose-derived stem cells (ADSCs) in medium supplemented with TGF-β3. 105 In summary, the recent research findings are contradictory, and no unanimous conclusions can be drawn.…”
Section: The Basal Role Of Tgf-β3 In the Life Cycle Of Chondrocytesmentioning
confidence: 95%
“…For the three-dimensional pellet culture, according to a previous study, 50 a cell suspension containing 2 × 10 6 BMSCs was centrifuged at 1100 rpm for 5 minutes in 15 ml centrifuge tubes, then the supernatant was removed and 2 ml of the growth medium was gently added into every tube without breaking the cell sediment. After static culture for 24 h, the pellets were cultured with the chondrogenic medium according to different conditions (GelMA or GelMA/KGN extracts).…”
Section: Methodsmentioning
confidence: 99%