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Cementum and enamel surface mimicry influences soft tissue cell behavior

Bellon, Benjamin; Pippenger, Benjamin; Stähli, Alexandra; Degen, Martin; Parisi, Ludovica (2024-06-03)

 
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J_of_Periodontal_Research_-_2024_-_Bellon_-_Cementum_and_enamel_surface_mimicry_influences_soft_tissue_cell_behavior.pdf (3.334Mt)
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Bellon, Benjamin
Pippenger, Benjamin
Stähli, Alexandra
Degen, Martin
Parisi, Ludovica
03.06.2024

JOURNAL OF PERIODONTAL RESEARCH
doi:10.1111/jre.13295
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202407197675

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Peer reviewed
Tiivistelmä
Aims: To test whether titanium surface roughness disparity might be used to specifically guide the behavior of gingiva fibroblasts and keratinocytes, thereby improving the quality of soft tissue (ST) integration around abutments. Methods: Titanium discs resembling the roughness of enamel (M) or cementum (MA) were created with normal or increased hydrophilicity and used as substrates for human fibroblasts and keratinocytes. Adhesion and proliferation assays were performed to assess cell-type specific responses upon encountering the different surfaces. Additionally, immunofluorescence and qPCR analyses were performed to study more in depth the behavior of fibroblasts and keratinocytes on MA and M surfaces, respectively. Results: While enamel-like M surfaces supported adhesion, growth and a normal differentiation potential of keratinocytes, cementum-emulating MA surfaces specifically impaired the growth of keratinocytes. Vice versa, MA surfaces sustained regular adhesion and proliferation of fibroblasts. Yet, a more intimate adhesion between fibroblasts and titanium was achieved by an increased hydrophilicity of MA surfaces, which was associated with an increased expression of elastin. Conclusion: The optimal titanium implant abutment might be achieved by a bimodal roughness design, mimicking the roughness of enamel (M) and cementum with increased hydrophilicity (hMA), respectively. These surfaces can selectively elicit cell responses favoring proper ST barrier by impairing epithelial downgrowth and promoting firm adhesion of fibroblasts.
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste