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The guardians of the periodontium-sequential and differential expression of antimicrobial peptides during gingival inflammation. Results from in vivo and in vitro studies.
Dommisch, Henrik; Skora, Philipp; Hirschfeld, Josefine; Olk, Gabriela; Hildebrandt, Laura; Jepsen, Søren.
Affiliation
  • Dommisch H; Department of Periodontology and Synoptic Dentistry, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Skora P; Department of Oral Health Sciences, University of Washington, Seattle, Washington.
  • Hirschfeld J; Department of Periodontology, Operative and Preventive Dentistry, University Hospital Bonn, Bonn, Germany.
  • Olk G; Department of Periodontology, Operative and Preventive Dentistry, University Hospital Bonn, Bonn, Germany.
  • Hildebrandt L; College of Medical and Dental Sciences, Periodontal Research Group, University of Birmingham, Birmingham, UK.
  • Jepsen S; Department of Periodontology, Operative and Preventive Dentistry, University Hospital Bonn, Bonn, Germany.
J Clin Periodontol ; 46(3): 276-285, 2019 03.
Article in En | MEDLINE | ID: mdl-30761574
AIM: To evaluate the sequential and differential expression of a variety of antimicrobial peptides (AMPs) during the development of an experimentally induced gingivitis in humans. MATERIAL AND METHODS: In twenty healthy volunteers, gingival inflammation was induced by abstention from oral hygiene at 6 teeth. Bleeding on probing (BOP) and plaque index (PI) were assessed, and gingival biopsies and gingival crevicular fluid (GCF) were collected at 8 different time points (t0-t35). Gingival epithelial cells (GECs) were stimulated with various receptor agonists. In biopsies and GECs, mRNA expression of human beta-defensins (hBD-2, hBD-3), CC-chemokine ligand 20 (CCL20), S100A7/psoriasin (S100A7), and calgranulin A/B (S100A8, S100A9) was evaluated using real-time PCR, and protein profiles were measured by ELISA. Statistical analysis was performed using non-parametric tests. RESULTS: The clinical parameters BOP, PI and GCF increased over time (p < 0.0001). Tissue AMP mRNA expression was elevated, but at different and AMP-specific time points (p < 0.05). Protein analysis revealed a similar expression pattern for hBD-2 and CCL20 in GCF (p < 0.05). In GECs, multiple receptor stimulation was required to induce AMP gene expression (p < 0.0001). CONCLUSIONS: For the first time, this study showed the sequential and differential expression of AMPs during a developing inflammation in vivo providing further evidence for their role as guardians of a healthy periodontium.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gingivitis / Anti-Infective Agents Limits: Humans Language: En Journal: J Clin Periodontol Year: 2019 Document type: Article Affiliation country: Germany Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gingivitis / Anti-Infective Agents Limits: Humans Language: En Journal: J Clin Periodontol Year: 2019 Document type: Article Affiliation country: Germany Country of publication: United States