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Differential response of human gingival fibroblasts to titanium‐ and titanium‐zirconium‐modified surfaces
Author(s) -
GómezFlorit M.,
Ramis J. M.,
Xing R.,
TaxtLamolle S.,
Haugen H. J.,
Lyngstadaas S. P.,
Monjo M.
Publication year - 2014
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/jre.12121
Subject(s) - extracellular matrix , wound healing , connective tissue , fibroblast , fibronectin , biocompatibility , titanium , chemistry , materials science , biomedical engineering , microbiology and biotechnology , pathology , medicine , biochemistry , immunology , metallurgy , biology , in vitro
Background and Objective Gingival fibroblasts are responsible for the constant adaptation, wound healing and regeneration of gingival connective tissue. New titanium‐zirconium (TiZr) abutment surfaces have been designed to improve soft tissue integration and reduce implant failure compared with titanium (Ti). The aim of the present study was first to characterize a primary human gingival fibroblast ( HGF ) model and secondly to evaluate their differential response to Ti and TiZr polished (P), machined (M) and machined + acid‐etched (mod MA ) surfaces, respectively. Material and Methods HGF were cultured on tissue culture plastic or on the different Ti and TiZr surfaces. Cell morphology was evaluated through confocal and scanning electron microscopy. A wound healing assay was performed to evaluate the capacity of HGF to close a scratch. The expression of genes was evaluated by real‐time RT ‐PCR, addressing: (i) extracellular matrix organization and turnover; (ii) inflammation; (iii) cell adhesion and structure; and (iv) wound healing. Finally, cells on Ti/TiZr surfaces were immunostained with anti‐ ITGB 3 antibodies to analyze integrin β3 production. Matrix metalloproteinase‐1 ( MMP 1) and inhibitor of metallopeptidases‐1 ( TIMP 1) production were analyzed by enzyme‐linked immunosorbent assays. Results On tissue culture plastic, HGF showed no differences between donors on cell proliferation and on the ability for wound closure; α‐smooth muscle actin was overexpressed on scratched monolayers. The differentiation profile showed increased production of extracellular matrix components. Ti and TiZr showed similar biocompatibility with HGF. TiZr increased integrin‐β3 mRNA and protein levels, compared with Ti. Cells on TiZr surfaces showed higher MMP1 protein than Ti surfaces, although similar TIMP1 protein production. In this in vitro experiment, P and M surfaces from both Ti and TiZr showed better HGF growth than modMA. Conclusion Taking into account the better mechanical properties and bioactivity of TiZr compared with Ti, the results of the present study show that TiZr is a potential clinical candidate for soft tissue integration and implant success.