IL-33 inhibits TNF-α-induced osteoclastogenesis and bone resorption

Fumitoshi Ohori, Hideki Kitaura, Saika Ogawa, Wei Ren Shen, Jiawei Qi, Takahiro Noguchi, Aseel Marahleh, Yasuhiko Nara, Adya Pramusita, Itaru Mizoguchi

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42 Citations (Scopus)


Interleukin (IL)-33 is a member of the IL-1 family, which acts as an alarmin. Several studies suggested that IL-33 inhibited osteoclastogenesis and bone resorption. Tumor necrosis factor-α (TNF-α) is considered a direct inducer of osteoclastogenesis. However, there has been no report regarding the effect of IL-33 on TNF-α-induced osteoclastogenesis and bone resorption. The objective of this study is to investigate the role of IL-33 on TNF-α-induced osteoclastogenesis and bone resorption. In an in vitro analysis of osteoclastogenesis, osteoclast precursors, which were derived from bone marrow cells, were treated with or without IL-33 in the presence of TNF-α. Tartrate-resistant acid phosphatase (TRAP) staining solution was used to assess osteoclast formation. In an in vivo analysis of mouse calvariae, TNF-α with or without IL-33 was subcutaneously administrated into the supracalvarial region of mice daily for 5 days. Histological sections were stained for TRAP, and osteoclast numbers were determined. Using micro-CT reconstruction images, the ratio of bone destruction area on the calvariae was evaluated. The number of TRAP-positive cells induced by TNF-α was significantly decreased with IL-33 in vitro and in vivo. Bone resorption was also reduced. IL-33 inhibited IκB phosphorylation and NF-κB nuclear translocation. These results suggest that IL-33 inhibited TNF-α-induced osteoclastogenesis and bone resorption.

Original languageEnglish
Article number1130
JournalInternational Journal of Molecular Sciences
Issue number3
Publication statusPublished - 1 Feb 2020
Externally publishedYes


  • IL-33
  • Osteoclast
  • Osteoclastogenesis
  • TNF-α


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