| Literature DB >> 22358541 |
Arei Miyamoto1, Masamichi Takami, Akifumi Matsumoto, Ayako Mochizuki, Takako Yamada, Keita Tachi, Isao Shibuya, Tomoya Nakamachi, Seiji Shioda, Kazuyoshi Baba, Tomio Inoue, Yoichi Miyamoto, Mijung Yim, Ryutaro Kamijo.
Abstract
R848, also known as resiquimod, acts as a ligand for toll-like receptor 7 (TLR7) and activates immune cells. In this study, we examined the effects of R848 on differentiation, survival, and bone-resorbing function of osteoclasts. R848 inhibited osteoclast differentiation of mouse bone marrow-derived macrophages (BMMs) and human peripheral blood-derived monocytes induced by receptor activator of NF-κB ligand in a dose-dependent manner. In addition, it inhibited mouse osteoclast differentiation induced in cocultures of bone marrow cells and osteoblasts in the presence of dihydroxyvitamin D(3) [1,25(OH)(2)D(3)]. However, R848 did not affect the survival or bone-resorbing activity of mouse mature osteoclasts. R848 also upregulated the mRNA expression levels of interleukin (IL)-6, IL-12, interferon (IFN)-γ, and inducible nitric oxide synthase in mouse BMMs expressing TLR7. IFN-β was consistently expressed in the BMMs and addition of neutralizing antibodies against IFN-β to the cultures partially recovered osteoclast differentiation inhibited by R848. These results suggest that R848 targets osteoclast precursors and inhibits their differentiation into osteoclasts via TLR7.Entities:
Year: 2012 PMID: 22358541 PMCID: PMC3386391 DOI: 10.1007/s10616-012-9442-5
Source DB: PubMed Journal: Cytotechnology ISSN: 0920-9069 Impact factor: 2.058