Volume 107, Issue 8 pp. 2549-2556
Original Research Report

Gingipains impair attachment of epithelial cell to dental titanium abutment surfaces

Sigrun Eick

Corresponding Author

Sigrun Eick

Department of Periodontology, School of Dental Medicine, University of Bern, CH-3010, Bern, Switzerland

Correspondence to: S. Eick; e-mail: [email protected]Search for more papers by this author
Naida Gadzo

Naida Gadzo

Department of Periodontology, School of Dental Medicine, University of Bern, CH-3010, Bern, Switzerland

These authors share the second position.Search for more papers by this author
Manuel Tacchi

Manuel Tacchi

Department of Periodontology, School of Dental Medicine, University of Bern, CH-3010, Bern, Switzerland

Present address: Department of Orthodontics and Dento-Facial Orthopedics, School of Dental Medicine, University of Bern, CH-3010 Bern, SwitzerlandThese authors share the second position.Search for more papers by this author
Anton Sculean

Anton Sculean

Department of Periodontology, School of Dental Medicine, University of Bern, CH-3010, Bern, Switzerland

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Jan Potempa

Jan Potempa

Department of Oral Immunology and Infectious Diseases, University of Louisville School of Dentistry, Louisville, Kentucky, USA

Department of Microbiology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Krakow, Poland

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Andreas Stavropoulos

Andreas Stavropoulos

Department of Periodontology, Faculty of Odontology, Malmö University, Malmö, Sweden

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First published: 14 February 2019
Citations: 5
Present address: Department of Orthodontics and Dento-Facial Orthopedics, School of Dental Medicine, University of Bern, CH-3010 Bern, Switzerland

Abstract

The study investigated in vitro the effect of Porphyromonas gingivalis and its cysteine proteases (gingipains) on epithelial cell adhesion to titanium–zirconium alloy surfaces. Titanium–zirconium discs with a standard machined (M) or chemically modified hydrophilic surface (modM) were coated with lamin-5 and incubated with telomerase-inactivated gingival keratinocytes (TIGK). Three P. gingivalis strains or gingipains were either added simultaneously with TIGK or after TIGK cells were already attached to the disks. Adhered TIGK cells were counted at 24 h. All P. gingivalis strains clearly inhibited adhesion of TIGK cells to M and modM surfaces. Compared with bacteria/gingipain-free TIGK cell cultures, the number of attached TIGK cells was reduced by about 80% and 60% when P. gingivalis was added simultaneously or after TIGK cells were already attached to the disks (each p < 0.01), respectively. Counts of attached cells were similarly reduced when only gingipains were used. Adhesion molecules of TIGK cells, in particular E-cadherin, were cleaved by P. gingivalis. In conclusion, P. gingivalis and gingipains interfere with the adhesion of epithelial cells to titanium–zirconium alloy surfaces by cleaving adhesion molecules, while a chemically modified hydrophilic titanium–zirconium alloy surface did not yield any protection. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B:2549–2556, 2019.

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