Back to Search Start Over

Hydroxyapatite–Silicon Scaffold Promotes Osteogenic Differentiation of CGF Primary Cells

Authors :
Laura Giannotti
Benedetta Di Chiara Stanca
Paola Nitti
Francesco Spedicato
Fabrizio Damiano
Christian Demitri
Nadia Calabriso
Maria Annunziata Carluccio
Andrea Palermo
Franco Ferrante
Luisa Siculella
Eleonora Stanca
Source :
Biology, Vol 12, Iss 4, p 528 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 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.

Details

Language :
English
ISSN :
20797737
Volume :
12
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.9dc53a14fe724d6291f654609bd4ee89
Document Type :
article
Full Text :
https://doi.org/10.3390/biology12040528