Expression of NOD2 is increased in inflamed human dental pulps and lipoteichoic acid-stimulated odontoblast-like cells

Author:

Keller Jean-François1,Carrouel Florence2,Staquet Marie-Jeanne3,Kufer Thomas A.4,Baudouin Caroline5,Msika Philippe5,Bleicher Françoise2,Farges Jean-Christophe1

Affiliation:

1. Université de Lyon, Université Lyon 1, Institut de Génomique Fonctionnelle de Lyon, UMR5242, CNRS, INRA, Ecole Normale Supérieure de Lyon, Groupe Odontoblastes et Régénération des Tissus Dentaires, Hospices Civils de Lyon, Service de Consultations et de Traitements Dentaires, Lyon, France

2. Université de Lyon, Université Lyon 1, Institut de Génomique Fonctionnelle de Lyon, UMR5242, CNRS, INRA, Ecole Normale Supérieure de Lyon, Groupe Odontoblastes et Régénération des Tissus Dentaires

3. Université de Lyon, Université Lyon 1, Institut de Génomique Fonctionnelle de Lyon, UMR5242, CNRS, INRA, Ecole Normale Supérieure de Lyon, Groupe Odontoblastes et Régénération des Tissus Dentaires, Institut Fédératif Biosciences Gerland Lyon Sud, Faculté d'Odontologie, Lyon, France,

4. Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany

5. Laboratoires Expanscience, Département Innovation, Recherche et Développement, Epernon, France

Abstract

Human odontoblasts trigger immune response s to oral bacteria that invade dental tissues during the caries process. To date, their ability to regulate the expression of the nucleotide-binding domain leucine-rich repeat containing receptor NOD2 when challenged by Gram-positive bacteria is unknown. In this study, we investigated NOD2 expression in healthy and inflamed human dental pulps challenged by bacteria, and in cultured odontoblast-like cells stimulated with lipoteichoic acid (LTA), a Toll-like receptor (TLR) 2 agonist which is specific for Gram-positive bacteria. We found that NOD2 gene expression was significantly up-regulated in pulps with acute inflammation compared to healthy ones. In vitro, LTA augmented NOD2 gene expression and protein level in odontoblast-like cells. The increase was more pronounced in odontoblast-like cells compared to dental pulp fibroblasts. Blocking experiments in odontoblast-like cells with anti-TLR2 antibody strongly reduced the NOD2 gene expression increase, whereas stimulation with the synthetic TLR2 ligand Pam2CSK4 confirmed NOD2 gene up-regulation following TLR2 engagement. These data suggest that NOD2 up-regulation is part of the odontoblast immune response to Gram-positive bacteria and might be important in protecting human dental pulp from the deleterious effects of cariogenic pathogens.

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

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