Premium
Endoplasmic reticulum stress response and bone loss in experimental periodontitis in mice
Author(s) -
Yamada H.,
Nakajima T.,
Domon H.,
Honda T.,
Yamazaki K.
Publication year - 2015
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/jre.12232
Subject(s) - endoplasmic reticulum , periodontitis , reticulum , medicine , dentistry , biology , microbiology and biotechnology
Background and Objective Endoplasmic reticulum ( ER ) stress is the cell response that activates the unfolded protein response ( UPR ) pathway in a variety of conditions, such as inflammation and bone metabolism. The UPR may be associated with the pathogenesis of periodontal disease because the disease is inflammatory in nature, and alveolar bone resorption is a characteristic feature of the disease. However, the relationship between ER stress and alveolar bone resorption observed in periodontal disease remains elusive. Material and Methods C57 BL /6 mice were orally administered Porphyromonas gingivalis , a representative periodontopathic bacterium, in the presence or absence of a chemical chaperone, 4‐phenylbutyrate (4‐ PBA ). The gene expression of UPR ‐related molecules and cytokines in gingival tissues were analyzed using real‐time polymerase chain reaction, and alveolar bone resorption and osteoclast numbers were evaluated histologically. The in vitro effect of 4‐ PBA on the differentiation of mouse bone marrow cells induced by receptor activator of nuclear factor‐κB ligand in the presence of macrophage colony‐stimulating factor was analyzed. Results The gene expression levels of UPR ‐related molecules and proinflammatory cytokines and alveolar bone resorption were significantly increased in P. gingivalis ‐administered mice. UPR ‐related gene expression and alveolar bone resorption were significantly suppressed by the administration of 4‐ PBA . However, no effect of 4‐ PBA was observed for proinflammatory cytokine expression in gingival tissues. Osteoclastic differentiation of bone marrow cells was also suppressed by 4‐ PBA with a concomitant reduction in the gene expression of cathepsin K and tartrate‐resistant alkaline phosphatase genes. Conclusion ER stress induced by oral administration of P. gingivalis is involved in alveolar bone resorption independent of inflammatory cytokines in mice.