Evaluation of the biological effects of amelogenin on human oral keratinocytes.

Augmentation Enamel matrix derivatives Keratinocytes Periodontal regeneration Regeneration

Journal

Dental materials : official publication of the Academy of Dental Materials
ISSN: 1879-0097
Titre abrégé: Dent Mater
Pays: England
ID NLM: 8508040

Informations de publication

Date de publication:
10 2023
Historique:
received: 14 06 2023
revised: 21 08 2023
accepted: 23 08 2023
medline: 25 9 2023
pubmed: 29 8 2023
entrez: 28 8 2023
Statut: ppublish

Résumé

Amelogenins are clinically used in periodontal regeneration as main components of root surface modifying agents, even without specifically preventing the premature colonization of the healing tissue defect by means of a physical barrier membrane. The objective of this study was to investigate the effects of human amelogenin on the proliferation, migration, and morphology of Immortalized Human Oral Keratinocytes (iHOKs). Immortalized Human Oral Keratinocytes were expanded in Keratinocyte Growth Medium-2 (KGM-2). Full-length recombinant amelogenin protein was diluted in KGM-2 in five concentrations (10 ng/ml, 100 ng/ml, 1.000 ng/ml, 5.000 ng/ml and 10.000 ng/ml). iHOKs were cultured in medium supplemented with the amelogenin dilutions. Samples without amelogenin served as control. Cell metabolism and cell proliferation together with cell migration were evaluated at day 7, 14, 21. At day 7, iHOKs treated with 10,000 ng/ml showed a significant decrease in keratinocytes´ proliferation. The metabolic activity at this timepoint was significantly lower for concentrations ≥ 1000 ng/ml. At days 14 and 21, both the addition of 5000 ng/ml and even more 10,000 ng/ml amelogenin reduced significantly the proliferation of keratinocytes. The effects on the metabolic activity for these timepoints were visible already with 100 ng/ml. Treatment of iHOKs with amelogenin of ≥ 1000 ng/ml led to inhibitory effects on cell migration already after 24 h. The full-length recombinant amelogenin has a significant biological impact on iHOKs. The increasing dose dependent inhibitory effects of amelogenin shown on iHOKs might explain the disruption of the apical migration of the junctional epithelium during regenerative healing. Amelogenin, presents time- and dose-dependent inhibitory effects on the growth of keratinocytes, which might explain the biological rationale behind its application in periodontal regeneration.

Identifiants

pubmed: 37640635
pii: S0109-5641(23)00369-X
doi: 10.1016/j.dental.2023.08.176
pii:
doi:

Substances chimiques

Amelogenin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

922-928

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Iris Frasheri (I)

Department of Conservative Dentistry and Periodontology University Hospital, LMU Munich, Germany. Electronic address: irisfrasheri@yahoo.it.

Maria Paschalidou (M)

Department of Conservative Dentistry and Periodontology University Hospital, LMU Munich, Germany; Department of Pediatric Dentistry, School of Dentistry, Faculty of Health Sciences, Aristotle University of Thessaloniki, Greece.

Thomas Imhof (T)

Center for Biochemistry II, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50931 Cologne, Germany; Institute for Dental Research and Oral Musculoskeletal Biology, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50931 Cologne, Germany.

Thorsten Steinberg (T)

Division of Oral Biotechnology, Center for Dental Medicine, Medical Center-University of Freiburg, Faculty of Medicine, Albert-Ludwigs-University of Freiburg, Hugstetter Str. 55, 79106 Freiburg, Germany.

Thomas Spinell (T)

Department of Conservative Dentistry and Periodontology University Hospital, LMU Munich, Germany.

Reinhard Hickel (R)

Department of Conservative Dentistry and Periodontology University Hospital, LMU Munich, Germany.

Matthias Folwaczny (M)

Department of Conservative Dentistry and Periodontology University Hospital, LMU Munich, Germany.

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Classifications MeSH