Alveolar Bone Protection by Targeting the SH3BP2-SYK Axis in Osteoclasts
-
- Mizuho Kittaka
- Indiana Center for Musculoskeletal Health Indiana University School of Medicine Indianapolis IN USA
-
- Tetsuya Yoshimoto
- Indiana Center for Musculoskeletal Health Indiana University School of Medicine Indianapolis IN USA
-
- Collin Schlosser
- Department of Orthodontics and Dentofacial Orthopedics University of Missouri-Kansas City, School of Dentistry Kansas City MO USA
-
- Robert Rottapel
- Department of Medicine, Immunology and Medical Biophysics University of Toronto Toronto Canada
-
- Mikihito Kajiya
- Department of Periodontal Medicine, Applied Life Sciences Institute of Biomedical and Health Sciences, Graduate School of Biomedical and Health Sciences, Hiroshima University Hiroshima Japan
-
- Hidemi Kurihara
- Department of Periodontal Medicine, Applied Life Sciences Institute of Biomedical and Health Sciences, Graduate School of Biomedical and Health Sciences, Hiroshima University Hiroshima Japan
-
- Ernst J Reichenberger
- Department of Reconstructive Sciences School of Dental Medicine, University of Connecticut Health Farmington CT USA
-
- Yasuyoshi Ueki
- Indiana Center for Musculoskeletal Health Indiana University School of Medicine Indianapolis IN USA
抄録
<jats:title>ABSTRACT</jats:title> <jats:p>Periodontitis is a bacterially induced chronic inflammatory condition of the oral cavity where tooth-supporting tissues including alveolar bone are destructed. Previously, we have shown that the adaptor protein SH3-domain binding protein 2 (SH3BP2) plays a critical role in inflammatory response and osteoclastogenesis of myeloid lineage cells through spleen tyrosine kinase (SYK). In this study, we show that SH3BP2 is a novel regulator for alveolar bone resorption in periodontitis. Micro-CT analysis of SH3BP2-deficient (Sh3bp2−/−) mice challenged with ligature-induced periodontitis revealed that Sh3bp2−/− mice develop decreased alveolar bone loss (male 14.9% ± 10.2%; female 19.0% ± 6.0%) compared with wild-type control mice (male 25.3% ± 5.8%; female 30.8% ± 5.8%). Lack of SH3BP2 did not change the inflammatory cytokine expression and osteoclast induction. Conditional knockout of SH3BP2 and SYK in myeloid lineage cells with LysM-Cre mice recapitulated the reduced bone loss without affecting both inflammatory cytokine expression and osteoclast induction, suggesting that the SH3BP2-SYK axis plays a key role in regulating alveolar bone loss by mechanisms that regulate the bone-resorbing function of osteoclasts rather than differentiation. Administration of a new SYK inhibitor GS-9973 before or after periodontitis induction reduced bone resorption without affecting inflammatory reaction in gingival tissues. In vitro, GS-9973 treatment of bone marrow–derived M-CSF-dependent macrophages suppressed tartrate-resistant acid phosphatase (TRAP)-positive osteoclast formation with decreased mineral resorption capacity even when GS-9973 was added after RANKL stimulation. Thus, the data suggest that SH3BP2-SYK is a novel signaling axis for regulating alveolar bone loss in periodontitis and that SYK can be a potential therapeutic target to suppress alveolar bone resorption in periodontal diseases. © 2019 American Society for Bone and Mineral Research. © 2019 American Society for Bone and Mineral Research.</jats:p>
収録刊行物
-
- Journal of Bone and Mineral Research
-
Journal of Bone and Mineral Research 35 (2), 382-395, 2019-10-15
Oxford University Press (OUP)