Wijekoon Suranji, Bwalya Eugene C, Fang Jing, Kim Sangho, Hosoya Kenji, Okumura Masahiro
Laboratory of Veterinary Surgery, Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.
J Vet Med Sci. 2017 Dec 22;79(12):2030-2035. doi: 10.1292/jvms.17-0393. Epub 2017 Nov 3.
The aim of this study was to investigate osteoclastogenic properties of inflammatory cytokines at different time-points of osteoclastogenesis. Bone marrow-derived macrophages from five healthy dogs were stimulated with the macrophage colony-stimulating factor, receptor activator of nuclear factor-κB ligand and inflammatory cytokines such as interleukin (IL)-1β, tumor necrosis factor (TNF)-α and IL-17. Osteoclasts (OC) formation and function were enhanced with TNF-α regardless of temporal differences. But in contrast, IL-1β suppressed the osteoclastogenesis at early phase of the process while upregulating at the late phase. Furthermore, differentiation of OC precursors into OC was suppressed at high concentrations of IL-17. Collectively, the results revealed that suppressing TNF-α would be a promising strategy to inhibit inflammation-associated bone destruction in dogs.
本研究的目的是在破骨细胞生成的不同时间点研究炎性细胞因子的破骨细胞生成特性。用巨噬细胞集落刺激因子、核因子κB受体激活剂配体和炎性细胞因子如白细胞介素(IL)-1β、肿瘤坏死因子(TNF)-α和IL-17刺激五只健康犬的骨髓来源巨噬细胞。无论时间差异如何,TNF-α均可增强破骨细胞(OC)的形成和功能。但相比之下,IL-1β在该过程的早期抑制破骨细胞生成,而在后期上调。此外,高浓度的IL-17可抑制OC前体细胞向OC的分化。总体而言,结果表明抑制TNF-α将是抑制犬炎症相关骨破坏的一种有前景的策略。