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Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice

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 c...

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Autores principales: Kittaka, Mizuho, Yoshimoto, Tetsuya, Schlosser, Collin, Kajiya, Mikihito, Kurihara, Hidemi, Reichenberger, Ernst J, Ueki, Yasuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285758/
https://www.ncbi.nlm.nih.gov/pubmed/32537546
http://dx.doi.org/10.1002/jbm4.10352
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author Kittaka, Mizuho
Yoshimoto, Tetsuya
Schlosser, Collin
Kajiya, Mikihito
Kurihara, Hidemi
Reichenberger, Ernst J
Ueki, Yasuyoshi
author_facet Kittaka, Mizuho
Yoshimoto, Tetsuya
Schlosser, Collin
Kajiya, Mikihito
Kurihara, Hidemi
Reichenberger, Ernst J
Ueki, Yasuyoshi
author_sort Kittaka, Mizuho
collection PubMed
description 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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spelling pubmed-72857582020-06-11 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 JBMR Plus Original Articles 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. John Wiley & Sons, Inc. 2020-04-14 /pmc/articles/PMC7285758/ /pubmed/32537546 http://dx.doi.org/10.1002/jbm4.10352 Text en © 2020 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kittaka, Mizuho
Yoshimoto, Tetsuya
Schlosser, Collin
Kajiya, Mikihito
Kurihara, Hidemi
Reichenberger, Ernst J
Ueki, Yasuyoshi
Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice
title Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice
title_full Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice
title_fullStr Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice
title_full_unstemmed Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice
title_short Microbe‐Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice
title_sort microbe‐dependent exacerbated alveolar bone destruction in heterozygous cherubism mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285758/
https://www.ncbi.nlm.nih.gov/pubmed/32537546
http://dx.doi.org/10.1002/jbm4.10352
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