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Comparison of the efficacy of piascledine and transforming growth factor β1 on chondrogenic differentiation of human adipose-derived stem cells in fibrin and fibrin-alginate scaffolds.
- Source :
-
Iranian journal of basic medical sciences [Iran J Basic Med Sci] 2018 Feb; Vol. 21 (2), pp. 212-218. - Publication Year :
- 2018
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Abstract
- Objectives: The aim of this study was to compare the chondrogenic induction potential of Piascledine and TGF-β1 on adipose-derived stem cells (ADSCs) in fibrin and fibrin-alginate scaffolds.<br />Materials and Methods: Human subcutaneous adipose tissues were harvested from three patients who were scheduled to undergo liposuction. Isolated ADSCs were proliferated in a culture medium. Then, the cells were seeded in fibrin or fibrin-alginate scaffolds and cultured for 14 days in a chondrogenic medium containing Piascledine, TGF-β1, or both. The rate of cell proliferation and survival was evaluated by using MTT [3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide] assay and the rate of the expression of type II collagen, aggrecan, and type X collagen genes was evaluated by real-time polymerase chain reaction (real-time PCR) method.<br />Results: The MTT results showed that Piascledine is able to enhance the proliferation and survival of ADSCs in fibrin scaffolds in comparison to other groups ( P <0.05). Real-time PCR evaluation revealed that the expression of type II collagen was higher in TGF- β1groups, but the expression of aggrecan was higher in TGF-β1 alone or along with Piascledine in fibrin-alginate scaffolds. Furthermore, the expression of type X collagen was lower in Piascledine alone or along with TGF-β1 in fibrin scaffold.<br />Conclusion: Piascledine can enhance the proliferation and differentiation of ADSCs in fibrin scaffolds.
Details
- Language :
- English
- ISSN :
- 2008-3866
- Volume :
- 21
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Iranian journal of basic medical sciences
- Publication Type :
- Academic Journal
- Accession number :
- 29456819
- Full Text :
- https://doi.org/10.22038/IJBMS.2018.24693.6136