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首页> 外文期刊>The Journal of Veterinary Medical Science >Chronological differential effects of pro-inflammatory cytokines on RANKL-induced osteoclast differentiation of canine bone marrow-derived macrophages
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Chronological differential effects of pro-inflammatory cytokines on RANKL-induced osteoclast differentiation of canine bone marrow-derived macrophages

机译:促炎细胞因子对RANKL诱导的犬骨髓来源巨噬细胞破骨细胞分化的时间差异

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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-?oB ligand and inflammatory cytokines such as interleukin (IL)-1?2, tumor necrosis factor (TNF)-?± and IL-17. Osteoclasts (OC) formation and function were enhanced with TNF-?± regardless of temporal differences. But in contrast, IL-1?2 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-?± would be a promising strategy to inhibit inflammation-associated bone destruction in dogs.
机译:这项研究的目的是调查破骨细胞形成的不同时间点的炎症细胞因子的破骨细胞特性。用巨噬细胞集落刺激因子,核因子-?oB配体的受体激活剂和炎性细胞因子(如白介素(IL)-1?2,肿瘤坏死因子(TNF)-?)刺激五只健康犬的骨髓巨噬细胞。 ±和IL-17。不论时间如何,TNF-α均能增强破骨细胞(OC)的形成和功能。但是相反,IL-1β2在该过程的早期抑制了破骨细胞生成,而在后期则上调。此外,在高浓度的IL-17中,OC前体向OC的分化受到抑制。总体而言,结果表明抑制TNF-α±将是抑制犬中与炎症相关的骨破坏的有前途的策略。

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