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Hydroxyapatite-Silicon Scaffold Promotes Osteogenic Differentiation of CGF Primary Cells.

Authors :
Giannotti L
Di Chiara Stanca B
Nitti P
Spedicato F
Damiano F
Demitri C
Calabriso N
Carluccio MA
Palermo A
Ferrante F
Siculella L
Stanca E
Source :
Biology [Biology (Basel)] 2023 Mar 30; Vol. 12 (4). Date of Electronic Publication: 2023 Mar 30.
Publication Year :
2023

Abstract

The application of scaffolding materials together with stem cell technologies plays a key role in tissue regeneration. Therefore, in this study, CGF (concentrated growth factor), which represents an autologous and biocompatible blood-derived product rich in growth factors and multipotent stem cells, was used together with a hydroxyapatite and silicon (HA-Si) scaffold, which represents a very interesting material in the field of bone reconstructive surgery. The aim of this work was to evaluate the potential osteogenic differentiation of CGF primary cells induced by HA-Si scaffolds. The cellular viability of CGF primary cells cultured on HA-Si scaffolds and their structural characterization were performed by MTT assay and SEM analysis, respectively. Moreover, the matrix mineralization of CGF primary cells on the HA-Si scaffold was evaluated through Alizarin red staining. The expression of osteogenic differentiation markers was investigated through mRNA quantification by real-time PCR. We found that the HA-Si scaffold was not cytotoxic for CGF primary cells, allowing their growth and proliferation. Furthermore, the HA-Si scaffold was able to induce increased levels of osteogenic markers, decreased levels of stemness markers in these cells, and the formation of a mineralized matrix. In conclusion, our results suggest that HA-Si scaffolds can be used as a biomaterial support for CGF application in the field of tissue regeneration.<br />Competing Interests: The authors declare no conflict of interest.

Details

Language :
English
ISSN :
2079-7737
Volume :
12
Issue :
4
Database :
MEDLINE
Journal :
Biology
Publication Type :
Academic Journal
Accession number :
37106729
Full Text :
https://doi.org/10.3390/biology12040528