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Mechanism of alveolar bone loss in a collagen‐induced arthritis model in mice
Author(s) -
Park JungChul,
Su Chuanxin,
Jung ImHee,
Choi SeongHo,
Cho KyooSung,
Kim ChongKwan,
Park YongBeom,
Lee SooKon,
Kim ChangSung
Publication year - 2011
Publication title -
journal of clinical periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.456
H-Index - 151
eISSN - 1600-051X
pISSN - 0303-6979
DOI - 10.1111/j.1600-051x.2010.01645.x
Subject(s) - collagen induced arthritis , dental alveolus , mechanism (biology) , arthritis , medicine , dentistry , immunology , philosophy , epistemology
Park J‐C, Su C, Jung I‐H, Choi S‐H, Cho K‐S, Kim C‐K, Park Y‐B, Lee S‐K, Kim C‐S: Mechanism of alveolar bone loss in a collagen‐induced arthritis model in mice. J Clin Periodontol 2011; 38: 122–130. doi: 10.1111/j.1600‐051X.2010.01645.x Abstract Objective: The aim of this study was to understand the cellular/molecular mechanisms of periodontal breakdown in a collagen‐induced arthritis (CIA) model in mice to enhance the understanding of rheumatoid arthritis (RA)‐associated alveolar bone loss in humans. Materials and Methods: All analyses were performed on paired samples from CIA and control group mice. Mandibles were retrieved for micro‐computed tomography (micro‐CT), histomorphometric analysis, and isolation of alveolar bone cells (ABCs). In vitro osteoclastogenic/osteogenic/adipogenic potentials of ABCs were evaluated and the mRNA expression of downstream effector genes was assessed. Bone formation of ABCs was assessed using an ectopic transplantation model. Results: Histomorphometric and micro‐CT data showed that alveolar bone loss was significantly increased in the CIA group ( p <0.05). Osteoclastogenesis was significantly increased in the CIA group in vivo ( p <0.05), with upregulated mRNA expressions of osteoclastogenesis‐associated genes. Osteoblasts appeared to undergo increased apoptosis, and the bone‐forming activity of ABCs concomitantly decreased with in vitro osteogenic differentiation and in vivo ectopic transplantation ( p <0.05). Also, adipogenesis‐associated mRNA expression was highly expressed in the CIA group, resulting in significantly enhanced adipocyte differentiation in vitro ( p <0.05). Conclusions: These data demonstrate that increased osteoclastic activity, decreased bone‐forming activity and enhanced adipogenesis promote alveolar bone loss in a CIA model in mice, and they suggest that these mechanisms could account for the same outcome in human RA.