Inhibition of non-canonical NF-kB signaling suppresses periodontal inflammation and bone loss

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  • 青木, 司
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野 九州大学大学院歯学研究院歯学部門口腔機能修復学歯周病学分野
  • 日浦, 史隆
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野
  • Li, Aonan
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野
  • Yang, Nan
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野
  • 髙倉, 那菜
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野
  • 向井, 悟
    東亜大学
  • 松田, 美穂
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野
  • 西村, 英紀
    九州大学大学院歯学研究院歯学部門口腔機能修復学歯周病学分野
  • 自見, 英治郎
    九州大学大学院歯学研究院歯学部門口腔常態制御学口腔細胞工学分野 九州大学大学院歯学研究院附属OBT研究センター

説明

Periodontal disease is an infectious disease that affects many people worldwide. Disease progression destroys the alveolar bone and causes tooth loss. We have previously shown that alymphoplasia (aly/aly) mice harboring a loss-of-function mutation in the map3k14 gene, which is involved in p100 to p52 processing of the alternative NF-κB pathway, exhibited mild osteopetrosis due to decreased number of osteoclasts, suggesting the alternative NF-κB pathway as a potential drug target for the amelioration of bone disease. In the present study, wild-type (WT) and aly/aly mice were subjected to silk ligation to establish a periodontitis model. Alveolar bone resorption was suppressed in aly/aly mice by decreased numbers of osteoclasts in the alveolar bone in comparison to WT mice. Furthermore, the expression of receptor activator of NF-κB ligand (RANKL) and TNFα (cytokines involved in osteoclast induction in periligative gingival tissue) was decreased. When primary osteoblasts (POBs) and bone marrow cells (BMCs) derived from WT and aly/aly mice were prepared and co-cultured, osteoclasts were induced from WT-derived BMCs, regardless of the origin of the POBs, but hardly formed from aly/aly mouse-derived BMCs. Furthermore, the local administration of an NIK inhibitor, Cpd33, inhibited osteoclast formation and thereby inhibited alveolar bone resorption in the periodontitis model. Therefore, the NIK-mediated NF-κB alternative pathway can be a therapeutic target for periodontal disease.

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詳細情報 詳細情報について

  • CRID
    1050862853910384000
  • ISSN
    16643224
  • HANDLE
    2324/7172190
  • 本文言語コード
    en
  • 資料種別
    journal article
  • データソース種別
    • IRDB

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