Takagi, Ryosuke Tokushima University
Sakamoto, Eijiro Tokushima University Tokushima University Educator and Researcher Directory
Kido, Jun-ichi Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Inagaki, Yuji Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Hiroshima, Yuka Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Naruishi, Koji Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Thesis or Dissertation
Objective: Calprotectin is hetero-complex of S100A8 and S100A9 and mainly secreted from neutrophils, monocytes and chondrocytes in inflammatory condition. Calprotectin binds to RAGE and TLR4, and induces the expression of pro-inflammatory chemokines and cytokines in various cells. Periodontitis is chronic inflammatory disease to lead gingival inflammation and alveolar bone resorption. Calprotectin levels in gingival crevicular fluid of periodontitis patients are higher than healthy patients. In the present study, the effects of S100A8 and S100A9 on the expressions of pro-inflammatory cytokines and bone metabolism related factor in mouse osteocyte like cells (MLO-Y4-A2) were investigated.
Design: MLO-Y4-A2 cells were treated with S100A8 and S100A9, and the expressions of RAGE, TLR4, RANKL and several inflammatory cytokines were analyzed by PCR and Western blotting or ELISA methods. To investigate the intracellular signaling pathways, phosphorylation of MAPK and STAT3 was determined by Western blotting, and chemical specific inhibitors and siRNAs were used.
Results: Expressions of IL-6 and RANKL were increased by treatment with S100A9 but not S100A8. However, both S100A8 and S100A9 did not changed expression of IL-1β, IL-8 and TNF-α. Although RAGE and TLR4 expressions were not up-regulated by S100A9 treatment, transfection of siRNA for RAGE and TLR4 significantly decreased IL-6 and RANKL expressions. In addition, S100A9 activated p38, ERK and STAT3 signaling pathways, and inhibitors for these factors significantly decreased S100A9 induced IL-6 and RANKL expressions.
Conclusions: These results indicated that S100A9 induces IL-6 and RANKL production via engagement with RAGE and TLR4 signalings in osteocytes and suggested that S100A9 may play important roles in the periodontal alveolar bone destruction.
BioMed Research International
内容要旨 : k3380_abstract.pdf
審査要旨 : k3380_review.pdf
論文本文 : k3380_fulltext.pdf (著者最終稿)
論文本文 : bmri_2020_7149408.pdf (雑誌掲載版)
本論文は, 著者Ryosuke Takagiの学位論文として提出され, 学位審査・授与の対象となっている。
© 2020 Ryosuke Takagi et al. This is an open access article distributed under the Creative Commons Attribution License,( https://creativecommons.org/licenses/by/4.0/ ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
|DOI (Published Version)|
|URL ( Publisher's Version )|
bmri_2020_7149408.pdf 1.48 MB
k3380_abstract.pdf 98.4 KB
k3380_review.pdf 57 KB
k3380_fulltext.pdf 462 KB
|MEXT report number||
Doctor of Dental Science
Institute of Advanced Medical Sciences