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Red-complex bacteria exhibit distinctly different interactions with human periodontal ligament stromal cells compared to Fusobacterium nucleatum.
Kendlbacher, Fabian L; Bloch, Susanne; Hager-Mair, Fiona F; Schäffer, Christina; Andrukhov, Oleh.
Afiliação
  • Kendlbacher FL; NanoGlycobiology Research Group, Institute of Biochemistry, Department of Chemistry, Universität für Bodenkultur Wien, Vienna, Austria.
  • Bloch S; NanoGlycobiology Research Group, Institute of Biochemistry, Department of Chemistry, Universität für Bodenkultur Wien, Vienna, Austria.
  • Hager-Mair FF; NanoGlycobiology Research Group, Institute of Biochemistry, Department of Chemistry, Universität für Bodenkultur Wien, Vienna, Austria.
  • Schäffer C; NanoGlycobiology Research Group, Institute of Biochemistry, Department of Chemistry, Universität für Bodenkultur Wien, Vienna, Austria. Electronic address: christina.schaeffer@boku.ac.at.
  • Andrukhov O; Competence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, A-1090 Vienna, Austria. Electronic address: oleh.andrukhov@meduniwien.ac.at.
Arch Oral Biol ; 164: 106004, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38776586
ABSTRACT

OBJECTIVE:

The red-complex bacteria Porphyromonas gingivalis and Tannerella forsythia together with Fusobacterium nucleatum are essential players in periodontitis. This study investigated the bacterial interplay with human periodontal ligament mesenchymal stromal cells (hPDL-MSCs) which act in the acute phase of periodontal infection.

DESIGN:

The capability of the bacteria to induce an inflammatory response as well as their viability, cellular adhesion and invasion were analyzed upon mono- and co-infections of hPDL-MSCs to delineate potential synergistic or antagonistic effects. The expression level and concentration of interleukin (IL)-6, IL-8 and monocyte chemoattractant protein (MCP)-1 were measured using qRT-PCR and ELISA. Viability, invasion, and adhesion were determined quantitatively using agar plate culture and qualitatively by confocal microscopy.

RESULTS:

Viability of P. gingivalis and T. forsythia but not F. nucleatum was preserved in the presence of hPDL-MSCs, even in an oxygenated environment. F. nucleatum significantly increased the expression and concentration of IL-6, IL-8 and MCP-1 in hPDL-MSCs, while T. forsythia and P. gingivalis caused only a minimal inflammatory response. Co-infections in different combinations had no effect on the inflammatory response. Moreover, P. gingivalis mitigated the increase in cytokine levels elicited by F. nucleatum. Both red-complex bacteria adhered to and invaded hPDL-MSCs in greater numbers than F. nucleatum, with only a minor effect of co-infections.

CONCLUSIONS:

Oral bacteria of different pathogenicity status interact differently with hPDL-MSCs. The data support P. gingivalis' capability to manipulate the inflammatory host response. Further research is necessary to obtain a comprehensive picture of the role of hPDL-MSCs in more complex oral biofilms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ligamento Periodontal / Interleucina-8 / Interleucina-6 / Fusobacterium nucleatum / Porphyromonas gingivalis / Quimiocina CCL2 / Tannerella forsythia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ligamento Periodontal / Interleucina-8 / Interleucina-6 / Fusobacterium nucleatum / Porphyromonas gingivalis / Quimiocina CCL2 / Tannerella forsythia Idioma: En Ano de publicação: 2024 Tipo de documento: Article