Aims: The first aim of this study was to characterize the surface topography of a novel 3D-printed dental implant at the micro-and macro-level. Its second aim was to evaluate the osteogenic, angiogenic, and immunogenic responses of human oral osteoblasts (hOBs), gingival fibroblasts (hGFs), mesenchymal stem cells (hAD-MSCs), and monocytes to this novel implant surface.Methods: A 3D-printed Ti-6Al-4 V implant was produced by selective laser melting and subjected to organic acid etching (TEST). It was then compared to a machined surface (CTRL). Its biological properties were evaluated via cell proliferation assays, morphological observations, gene expression analyses, mineralization assessments, and collagen quantifications.Results: Scanning electron microscopy analysis showed that the TEST group was characterized by a highly interconnected porous architecture and a roughed surface. The morphological observations showed good adhesion of cells cultured on the TEST surface, with a significant increase in hOB growth. Similarly, the gene expression analysis showed significantly higher levels of osseointegration biomarkers. Picrosirius staining showed a slight increase in collagen production in the TEST group compared to the CTRL group. hAD-MSCs showed an increase in endothelial and osteogenic commitment-related markers. Monocytes showed increased mRNA synthesis related to the M2 (anti-inflammatory) macrophagic phenotype.Conclusions: Considering the higher interaction with hOBs, hGFs, hAD-MSCs, and monocytes, the prepared 3D -printed implant could be used for future clinical applications. Clinical relevance: This study demonstrated the excellent biological response of various cells to the porous surface of the novel 3D-printed implant.

3D printed dental implants with a porous structure: The in vitro response of osteoblasts, fibroblasts, mesenchymal stem cells, and monocytes

Iezzi, Giovanna
Primo
;
Petrini, Morena;Pierfelice, Tania Vanessa;D'Amico, Emira
Penultimo
;
2024-01-01

Abstract

Aims: The first aim of this study was to characterize the surface topography of a novel 3D-printed dental implant at the micro-and macro-level. Its second aim was to evaluate the osteogenic, angiogenic, and immunogenic responses of human oral osteoblasts (hOBs), gingival fibroblasts (hGFs), mesenchymal stem cells (hAD-MSCs), and monocytes to this novel implant surface.Methods: A 3D-printed Ti-6Al-4 V implant was produced by selective laser melting and subjected to organic acid etching (TEST). It was then compared to a machined surface (CTRL). Its biological properties were evaluated via cell proliferation assays, morphological observations, gene expression analyses, mineralization assessments, and collagen quantifications.Results: Scanning electron microscopy analysis showed that the TEST group was characterized by a highly interconnected porous architecture and a roughed surface. The morphological observations showed good adhesion of cells cultured on the TEST surface, with a significant increase in hOB growth. Similarly, the gene expression analysis showed significantly higher levels of osseointegration biomarkers. Picrosirius staining showed a slight increase in collagen production in the TEST group compared to the CTRL group. hAD-MSCs showed an increase in endothelial and osteogenic commitment-related markers. Monocytes showed increased mRNA synthesis related to the M2 (anti-inflammatory) macrophagic phenotype.Conclusions: Considering the higher interaction with hOBs, hGFs, hAD-MSCs, and monocytes, the prepared 3D -printed implant could be used for future clinical applications. Clinical relevance: This study demonstrated the excellent biological response of various cells to the porous surface of the novel 3D-printed implant.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/828031
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