Improving dental epithelial junction on dental implants with bioengineered peptides

Introduction: The functionalization of titanium (Ti) and titanium alloys (Ti6Al4V) implant surfaces via material-specific peptides influence host/biomaterial interaction. The impact of using peptides as molecular linkers between cells and implant material to improve keratinocyte adhesion is reported...

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Main Authors: Ivan V. Panayotov, Attila G. Végh, Marta Martin, Boyan Vladimirov, Christian Larroque, Csilla Gergely, Frédéric J. G. Cuisinier, Elias Estephan
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-06-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2023.1165853/full
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author Ivan V. Panayotov
Ivan V. Panayotov
Attila G. Végh
Marta Martin
Boyan Vladimirov
Christian Larroque
Csilla Gergely
Frédéric J. G. Cuisinier
Frédéric J. G. Cuisinier
Elias Estephan
Elias Estephan
author_facet Ivan V. Panayotov
Ivan V. Panayotov
Attila G. Végh
Marta Martin
Boyan Vladimirov
Christian Larroque
Csilla Gergely
Frédéric J. G. Cuisinier
Frédéric J. G. Cuisinier
Elias Estephan
Elias Estephan
author_sort Ivan V. Panayotov
collection DOAJ
description Introduction: The functionalization of titanium (Ti) and titanium alloys (Ti6Al4V) implant surfaces via material-specific peptides influence host/biomaterial interaction. The impact of using peptides as molecular linkers between cells and implant material to improve keratinocyte adhesion is reported.Results: The metal binding peptides (MBP-1, MBP-2) SVSVGMKPSPRP and WDPPTLKRPVSP were selected via phage display and combined with laminin-5 or E-cadherin epithelial cell specific peptides (CSP-1, CSP-2) to engineer four metal-cell specific peptides (MCSPs). Single-cell force spectroscopy and cell adhesion experiments were performed to select the most promising candidate. In vivo tests using the dental implant for rats showed that the selected bi functional peptide not only enabled stable cell adhesion on the trans-gingival part of the dental implant but also arrested the unwanted apical migration of epithelial cells.Conclusion: The results demonstrated the outstanding performance of the bioengineered peptide in improving epithelial adhesion to Ti based implants and pointed towards promising new opportunities for applications in clinical practice.
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spelling doaj.art-54367483c62340259b93f1f365906c2b2023-06-20T10:04:20ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852023-06-011110.3389/fbioe.2023.11658531165853Improving dental epithelial junction on dental implants with bioengineered peptidesIvan V. Panayotov0Ivan V. Panayotov1Attila G. Végh2Marta Martin3Boyan Vladimirov4Christian Larroque5Csilla Gergely6Frédéric J. G. Cuisinier7Frédéric J. G. Cuisinier8Elias Estephan9Elias Estephan10LBN, University Montpellier, Montpellier, FranceCSERD, CHU Montpellier, Montpellier, FranceBiological Research Centre, Institute of Biophysics, Eötvös Lóránd Research Network (ELKH), Szeged, HungaryL2C, University Montpellier, CNRS, Montpellier, FranceDepartment of Maxillofacial Surgery, Medical University of Plovdiv, Plovdiv, BulgariaDepartment of Nephrology, CHU Montpellier, Hôpital Lapeyronie, IRMB, University of Montpellier, INSERM U1183, Montpellier, FranceL2C, University Montpellier, CNRS, Montpellier, FranceLBN, University Montpellier, Montpellier, FranceCSERD, CHU Montpellier, Montpellier, FranceLBN, University Montpellier, Montpellier, FranceNeuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, LebanonIntroduction: The functionalization of titanium (Ti) and titanium alloys (Ti6Al4V) implant surfaces via material-specific peptides influence host/biomaterial interaction. The impact of using peptides as molecular linkers between cells and implant material to improve keratinocyte adhesion is reported.Results: The metal binding peptides (MBP-1, MBP-2) SVSVGMKPSPRP and WDPPTLKRPVSP were selected via phage display and combined with laminin-5 or E-cadherin epithelial cell specific peptides (CSP-1, CSP-2) to engineer four metal-cell specific peptides (MCSPs). Single-cell force spectroscopy and cell adhesion experiments were performed to select the most promising candidate. In vivo tests using the dental implant for rats showed that the selected bi functional peptide not only enabled stable cell adhesion on the trans-gingival part of the dental implant but also arrested the unwanted apical migration of epithelial cells.Conclusion: The results demonstrated the outstanding performance of the bioengineered peptide in improving epithelial adhesion to Ti based implants and pointed towards promising new opportunities for applications in clinical practice.https://www.frontiersin.org/articles/10.3389/fbioe.2023.1165853/fullbioengineered peptidephage displayimplantstitanium surface functionalizationepithelial adhesion
spellingShingle Ivan V. Panayotov
Ivan V. Panayotov
Attila G. Végh
Marta Martin
Boyan Vladimirov
Christian Larroque
Csilla Gergely
Frédéric J. G. Cuisinier
Frédéric J. G. Cuisinier
Elias Estephan
Elias Estephan
Improving dental epithelial junction on dental implants with bioengineered peptides
Frontiers in Bioengineering and Biotechnology
bioengineered peptide
phage display
implants
titanium surface functionalization
epithelial adhesion
title Improving dental epithelial junction on dental implants with bioengineered peptides
title_full Improving dental epithelial junction on dental implants with bioengineered peptides
title_fullStr Improving dental epithelial junction on dental implants with bioengineered peptides
title_full_unstemmed Improving dental epithelial junction on dental implants with bioengineered peptides
title_short Improving dental epithelial junction on dental implants with bioengineered peptides
title_sort improving dental epithelial junction on dental implants with bioengineered peptides
topic bioengineered peptide
phage display
implants
titanium surface functionalization
epithelial adhesion
url https://www.frontiersin.org/articles/10.3389/fbioe.2023.1165853/full
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