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Hydrofluoric acid treatment of titanium surfaces enhances the proliferation of human gingival fibroblasts.


ABSTRACT: The attachment of implants relies on bone and soft tissue biocompatibility. The aim of this article is to investigate the effect of fluoride-modified metallic titanium (Ti) surfaces (Ti-F) on proliferation and differentiation of human gingival fibroblasts. Human gingival fibroblast cells were exposed to hydrofluoric acid-modified Ti coins (Ti-F) for 1, 3, 7, 14 and 21?days, and untreated coins were used as controls. A five- to six-fold increase in the proliferation of human gingival fibroblasts on Ti-F compared to Ti surfaces was observed. Enhanced gene expression of interleukin-6 and osteoprotegerin was found at 7?days. Increased levels of sclerostin, interleukin-6 and osteoprotegerin in the media from human gingival fibroblasts cultured on Ti-F coins were found compared to controls. Our results confirm that hydrofluoric acid-modified surface may indirectly enhance the firm attachment of implant surface to junction epithelium, soft tissue epithelium, which would give protection for underlying osseous structures making osseointegration of the dental implant possible.

SUBMITTER: Pham MH 

PROVIDER: S-EPMC6378639 | biostudies-literature | 2019 Jan-Dec

REPOSITORIES: biostudies-literature

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Hydrofluoric acid treatment of titanium surfaces enhances the proliferation of human gingival fibroblasts.

Pham Maria H MH   Haugen Håvard J HJ   Rinna Alessandra A   Ellingsen Jan Eirik JE   Reseland Janne E JE  

Journal of tissue engineering 20190101


The attachment of implants relies on bone and soft tissue biocompatibility. The aim of this article is to investigate the effect of fluoride-modified metallic titanium (Ti) surfaces (Ti-F) on proliferation and differentiation of human gingival fibroblasts. Human gingival fibroblast cells were exposed to hydrofluoric acid-modified Ti coins (Ti-F) for 1, 3, 7, 14 and 21 days, and untreated coins were used as controls. A five- to six-fold increase in the proliferation of human gingival fibroblasts  ...[more]

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