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Comparative impact of platelet rich plasma and transforming growth factor-β on chondrogenic differentiation of human adipose derived stem cells

Authors :
Mahboubeh Kabiri
Rezvan Tavakoli
Fatemeh Kouhkan
Mina Keshvarinia
Soheila Zamanluee
Roya Hesari
Kazem Parivar
Iman Rad
Hoorieh Hoseinpoor
Masoud Soleimani
Hana Hanaee-Ahvaz
Source :
BioImpacts : BI, BioImpacts, Vol 10, Iss 1, Pp 37-43 (2020)
Publication Year :
2019
Publisher :
Maad Rayan Publishing Company, 2019.

Abstract

Introduction: Transforming growth factor-beta (TGF-β) is known as standard chondrogenic differentiation agent, even though it comes with undesirable side effects such as early hypertrophic maturation, mineralization, and secretion of inflammatory/angiogenic factors. On the other hand, platelet-rich plasma (PRP) is found to have a chondrogenic impact on mesenchymal stem cell proliferation and differentiation, with no considerable side effects. Therefore, we compared chondrogenic impact of TGF-β and PRP on adipose-derived stem cells (ADSCs), to see if PRP could be introduced as an alternative to TGF-β. Methods: Differentiation of ADSCs was monitored using a couple of methods including glycosaminoglycan production, miRNAs expression, vascular endothelial growth factor (VEGF)/tumor necrosis factor alpha (TNFα) secretion, alkaline phosphatase (ALP) and calcium content assays. Results: Accordingly, the treatment of differentiating cells with 5% (v/v) PRP resulted in higher glycosaminoglycan production, enhanced SOX9 transcription, and lowered TNFα and VEGF secretion compared to the control and TGF-β groups. Besides, the application of PRP to the media up-regulated miR-146a and miR-199a in early and late stages of chondrogenesis, respectively. Conclusion: PRP induces in vitro chondrogenesis, as well as TGF-β with lesser inflammatory and hypertrophic side effects.

Details

ISSN :
22285652 and 22285660
Volume :
10
Database :
OpenAIRE
Journal :
BioImpacts
Accession number :
edsair.doi.dedup.....b77479fdea10ca6f58be2e30ca432837
Full Text :
https://doi.org/10.15171/bi.2020.05