The virulence factor GroEL promotes gelatinase secretion from cells in the osteoblast lineage: Implication for direct crosstalk between bacteria and adult cells. (February 2021)

• Record Type: Journal Article
• Authors: Zhang, Li; Cui, Yujia; Yang, Yueyi; Wei, Jieya; Liu, Wenjing; Cai, Linyi; Wang, Luling; Zhang, Demao; Xie, Jing; Cheng, Lei
• Is Part Of: Archives of oral biology. Volume 122(2021)
• Publication Date: 2021-02
• Subjects: GroEL -- Osteoblasts -- Crosstalk -- MMP-2 -- MMP-9 -- Inflammation; Mouth -- Periodicals; Mouth -- Diseases -- Periodicals; Dentistry -- Periodicals; Electronic journals; 617.6005
• DOI: 10.1016/j.archoralbio.2020.104991
• Languages: English
• ISSNs: 0003-9969

Abstract

Highlights: GroEL, a metabolite from oral flora, is elevated in saliva and periapical tissues from patients with apical periodontitis. GroEL influences osteoblast cell function by characterizing the changes of secreted gelatinases. GroEL induced the activation of NF-κB signaling in osteoblasts. Abstract: Objective: The aim of this study was to demonstrate the influence of the virulence factor GroEL on osteoblast behavior by characterizing the changes of secreted gelatinases. Design: ELISA was performed to detect GroEL from samples from patients with or without apical periodontitis. An apical periodontitis model was established in rats and the expression of MMP-2, MMP-9 and NF-κB was evaluated by immunofluorescence staining. The primary osteoblasts and osteoblast-like MC3T3 cells were stimulated with recombinant GroEL, and gelatin zymography was used to determine the activity and expression of MMP-2 and MMP-9. Western blot was used to screen signaling pathways, and immunofluorescence staining was performed to confirm the activated signaling. Results: First, we found expression of GroEL to be higher in oral saliva, gingival crevicular fluid and periradicular granulation tissue of patients with apical periodontitis than it was in healthy control patients. We next found that recombinant GroEL could increase the activity of the gelatinases, MMP-2 and MMP-9, which were secreted by both primary osteoblasts and MC3T3 cells. In a rat apical periodontitis model, strong expression of gelatinases was confirmed. Then, we found that GroEL-enhanced gelatinase activity was mediated through activation of NF-κB signaling. Acetylated NF-κB accumulated in the cell nucleus and bound to the promoter of MMP-2 and MMP-9 genes, thus initiating their high expression. Conclusion: This study reveals a direct interaction between oral bacteria and adult cells by demonstrating that gelatinase secretion is induced by GroEL, which partially explains bone resorption through gelatinase activation.