Advanced-platelet-rich fibrin extract promotes adipogenic and osteogenic differentiation of human adipose-derived stem cells in a dose-dependent manner in vitro. (August 2021)

• Record Type: Journal Article
• Authors: Liang, Zhijie; Huang, Donglin; Nong, Wenhai; Mo, Jinping; Zhu, Dandan; Wang, Mengxin; Chen, Maojian; Wei, Changyuan; Li, Hongmian
• Is Part Of: Tissue & cell. Volume 71(2021)
• Publication Date: 2021-08
• Subjects: Advanced-platelet-rich fibrin extract -- Adipose-derived stem cells -- Differentiation -- Paracrine; Cytology -- Periodicals; 571.5
• DOI: 10.1016/j.tice.2021.101506
• Languages: English
• ISSNs: 0040-8166

Abstract

Highlights: Adipose-derived stem cells (ASCs) possess the function of polydifferentiation. A-PRF gradually secreted extract containing various cytokines such as VEGF, TGF-β1 and IL-1β, and the levels peaked at day 7. A-PRFe significantly promote proliferation, paracrine function and adipogenic/osteogenic differentiation of ASCs in a dose-dependent manner. Abstract: Advanced platelet-rich fibrin (A-PRF) is an autogenous biological material obtained from peripheral blood. A-PRF extract (A-PRFe) contains a high concentration of various cytokines that are increasingly appreciated for their roles in improving stem cell repairing function during tissue regeneration. However, the optimal A-PRFe concentration to stimulate stem cells is unknown. This study aimed to identify the optimal concentrations of A-PRFe to promote adipogenic and osteogenic differentiation of human adipose-derived stem cells (ASCs). We produced A-PRFe from A-PRF clots by centrifuging fresh peripheral blood samples and isolated and identified ASCs using surface CD markers and multilineage differentiation potential. Enzyme-linked immunosorbent assay (ELISA) showed the concentrations of several cytokines, including b-FGF, PDGF-BB, and others, increased gradually, peaked on day 7 and then decreased. Cell proliferation assays showed A-PRFe significantly stimulated ASC proliferation, and proliferation significantly increased at higher A-PRFe doses. The degree of adipogenic and osteogenic differentiation increased at higher A-PRFe concentrations in the culture medium, as determined by oil red O and alizarin red staining. Reverse transcription polymerase chain reaction (RT-PCR) showed that expression levels of genes related to adipogenic/osteogenic differentiation (PPARγ2, C/EBPα, FABP4, Adiponectin, and ALP, OPN, OCN, RUNX2), paracrine (HIF-1α, VEGF, IGF-2) and immunoregulation (HSP70, IL-8) function were higher in groups with a higher concentration of A-PRFe than in lower concentration groups. This study demonstrates that A-PRFe is ideal for use in ASC applications in regenerative medicine because it improves biological functions, including proliferation, adipogenic/osteogenic differentiation, and paracrine function in a dose-dependent manner.