Literature DB >> 29531138

Anti-HMGB1 Neutralizing Antibody Attenuates Periodontal Inflammation and Bone Resorption in a Murine Periodontitis Model.

Chiaki Yoshihara-Hirata1, Keisuke Yamashiro1, Tadashi Yamamoto1, Hiroaki Aoyagi1, Hidetaka Ideguchi1, Mari Kawamura1, Risa Suzuki1, Mitsuaki Ono2, Hidenori Wake3, Masahiro Nishibori3, Shogo Takashiba4.   

Abstract

High mobility group box 1 (HMGB1) is a non-histone DNA-binding protein that is secreted into the extracellular milieu in response to inflammatory stimuli. The secreted HMGB1 mediates various inflammatory diseases, including periodontitis; however, the underlying mechanisms of HMGB1-induced periodontal inflammation are not completely understood. Here, we examined whether anti-HMGB1 neutralizing antibody inhibits periodontal progression and investigated the molecular pathology of HMGB1 in vitro and in vivo. In vitro analysis indicated that HMGB1, granulocyte-macrophage colony-stimulating factor (GM-CSF), and interleukin-1β (IL-1β) were secreted in response to tumor necrosis factor-α (TNF-α) stimuli in human gingival epithelial cells (HGECs) and human monocytic leukemia cells (THP-1) treated with phorbol myristate acetate. Increased levels of GM-CSF and IL-1β were observed in the conditioned media from TNF-α-stimulated HGECs and THP-1 in vitro Simultaneous stimulation with TNF-α and anti-HMGB1 antibody significantly decreased TNF-α-induced inflammatory cytokine secretion. Experimental periodontitis was induced in mice using Porphyromonas gingivalis-soaked ligatures. The extracellular translocation was confirmed in gingival epithelia in the periodontitis model mice by immunofluorescence analysis. Systemic administration of anti-HMGB1 neutralizing antibody significantly inhibited translocation of HMGB1. The anti-HMGB1 antibody inhibited periodontal inflammation, expression of IL-1β and C-X-C motif chemokine ligand 1 (CXCL1), migration of neutrophils, and bone resorption, shown by bioluminescence imaging of myeloperoxidase activity, quantitative reverse transcription-PCR (RT-PCR), and micro-computed tomography analysis. These findings indicate that HMGB1 is secreted in response to inflammatory stimuli caused by periodontal infection, which is crucial for the initiation of periodontitis, and the anti-HMGB1 antibody attenuates the secretion of a series of inflammatory cytokines, consequently suppressing the progression of periodontitis.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  bone resorption; cytokine; infectious disease; molecular imaging; periodontal disease

Mesh:

Substances:

Year:  2018        PMID: 29531138      PMCID: PMC5913859          DOI: 10.1128/IAI.00111-18

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  33 in total

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6.  Tumor necrosis factor-alpha stimulates gingival epithelial cells to release high mobility-group box 1.

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Review 8.  Extracellular role of HMGB1 in inflammation and sepsis.

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6.  Inhibition of HMGB1 Promotes Osseointegration under Hyperglycemic Condition through Improvement of BMSC Dysfunction.

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Review 9.  High Mobility Group Box 1 Expression in Oral Inflammation and Regeneration.

Authors:  Keisuke Yamashiro; Hidetaka Ideguchi; Hiroaki Aoyagi; Chiaki Yoshihara-Hirata; Anna Hirai; Risa Suzuki-Kyoshima; Yao Zhang; Hidenori Wake; Masahiro Nishibori; Tadashi Yamamoto; Shogo Takashiba
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10.  High-Mobility Group Box 1 Expression in Mandibular Bone Cells of Experimental Periodontitis.

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