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Microbe-Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice.
Kittaka, Mizuho; Yoshimoto, Tetsuya; Schlosser, Collin; Kajiya, Mikihito; Kurihara, Hidemi; Reichenberger, Ernst J; Ueki, Yasuyoshi.
Affiliation
  • Kittaka M; Department of Biomedical Sciences and Comprehensive Care Indiana University School of Dentistry Indianapolis IN USA.
  • Yoshimoto T; Indiana Center for Musculoskeletal Health Indiana University School of Medicine Indianapolis IN USA.
  • Schlosser C; Department of Biomedical Sciences and Comprehensive Care Indiana University School of Dentistry Indianapolis IN USA.
  • Kajiya M; Indiana Center for Musculoskeletal Health Indiana University School of Medicine Indianapolis IN USA.
  • Kurihara H; Department of Orthodontics and Dentofacial Orthopedics University of Missouri-Kansas City, School of Dentistry Kansas City MO USA.
  • Reichenberger EJ; Department of Periodontal Medicine, Applied Life Sciences Institute of Biomedical & Health Sciences, Graduate School of Biomedical & Health Sciences, Hiroshima University Hiroshima Japan.
  • Ueki Y; Department of Periodontal Medicine, Applied Life Sciences Institute of Biomedical & Health Sciences, Graduate School of Biomedical & Health Sciences, Hiroshima University Hiroshima Japan.
JBMR Plus ; 4(6): e10352, 2020 Jun.
Article in En | MEDLINE | ID: mdl-32537546
Cherubism (OMIM#118400) is a craniofacial disorder characterized by destructive jaw expansion. Gain-of-function mutations in SH3-domain binding protein 2 (SH3BP2) are responsible for this rare disorder. We have previously shown that homozygous knock-in (KI) mice (Sh3bp2 KI/KI ) recapitulate human cherubism by developing inflammatory lesions in the jaw. However, it remains unknown why heterozygous KI mice (Sh3bp2 KI/+ ) do not recapitulate the excessive jawbone destruction in human cherubism, even though all mutations are heterozygous in humans. We hypothesized that Sh3bp2 KI/+ mice need to be challenged for developing exacerbated jawbone destruction and that bacterial stimulation in the oral cavity may be involved in the mechanism. In this study, we applied a ligature-induced periodontitis model to Sh3bp2 KI/+ mice to induce inflammatory alveolar bone destruction. Ligature placement induced alveolar bone resorption with gingival inflammation. Quantification of alveolar bone volume revealed that Sh3bp2 KI/+ mice developed more severe bone loss (male: 43.0% ± 10.6%, female: 42.6% ± 10.4%) compared with Sh3bp2 +/+ mice (male: 25.8% ± 4.0%, female: 30.9% ± 6.5%). Measurement of bone loss by the cement-enamel junction-alveolar bone crest distance showed no difference between Sh3bp2 KI/+ and Sh3bp2 +/+ mice. The number of osteoclasts on the alveolar bone surface was higher in male Sh3bp2 KI/+ mice, but not in females, compared with Sh3bp2 +/+ mice. In contrast, inflammatory cytokine levels in gingiva were comparable between Sh3bp2 KI/+ and Sh3bp2 +/+ mice with ligatures. Genetic deletion of the spleen tyrosine kinase in myeloid cells and antibiotic treatment suppressed alveolar bone loss in Sh3bp2 KI/+ mice, suggesting that increased osteoclast differentiation and function mediated by SYK and accumulation of oral bacteria are responsible for the increased alveolar bone loss in Sh3bp2 KI/+ mice with ligature-induced periodontitis. High amounts of oral bacterial load caused by insufficient oral hygiene could be a trigger for the initiation of jawbone destruction in human cherubism. © 2020 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JBMR Plus Year: 2020 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JBMR Plus Year: 2020 Document type: Article Country of publication: United kingdom