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压缩机械力通过激活 c-Fms 介导的信号增强破骨细胞生成,这是由骨髓巨噬细胞完成的。

Compressive mechanical force augments osteoclastogenesis by bone marrow macrophages through activation of c-Fms-mediated signaling.

机构信息

Institute of Oral Biosciences and BK21 Program, Chonbuk National University, Jeonju 561-756, South Korea.

出版信息

J Cell Biochem. 2010 Dec 1;111(5):1260-9. doi: 10.1002/jcb.22849.

DOI:10.1002/jcb.22849
PMID:20803546
Abstract

Little is known about the effects of mechanical forces on osteoclastogenesis by bone marrow macrophages (BMMs) in the absence of mechanosensitive cells, including osteoblasts and fibroblasts. In this study, we examined the effects of mechanical force on osteoclastogenesis by applying centrifugal force to BMMs using a horizontal microplate rotor. Our findings, as measured by an in vitro model system, show that tumor necrosis factor (TNF)-α is capable of inducing osteoclast differentiation from BMMs and bone resorption in the presence of macrophage-colony stimulating factor (M-CSF) and is further facilitated by receptor activator of nuclear factor-kappaB (NF-κB) ligand (RANKL). Application of force to BMMs accelerated TNF-α-induced osteoclastogenesis; this was inhibited either by anti-TNF-α or anti-TNF-α receptor but not by OPG. TNF-α also increased c-Fms expression at both mRNA and protein levels in BMMs. An anti-c-Fms antibody completely inhibited osteoclast differentiation and bone resorption induced by TNF-α but partially blocked osteoclastogenesis stimulated in combination with RANKL. These results suggest that TNF-α (in the presence of M-CSF) is capable of inducing osteoclastogenesis from BMMs, and that osteoclastogenesis is significantly stimulated by force application through the activation of c-Fms-mediated signaling. Overall, the present study reveals the facilitating effect of mechanical force on osteoclastic differentiation from BMMs without the addition of mechanosensitive cells.

摘要

目前对于在缺乏机械敏感细胞(包括成骨细胞和成纤维细胞)的情况下,骨髓巨噬细胞(BMM)中的机械力对破骨细胞形成的影响知之甚少。在这项研究中,我们使用水平微板转子对 BMM 施加离心力,研究了机械力对破骨细胞形成的影响。我们的发现,通过体外模型系统测量,表明肿瘤坏死因子(TNF)-α能够在巨噬细胞集落刺激因子(M-CSF)存在的情况下诱导 BMM 分化为破骨细胞并进行骨吸收,而核因子κB 受体激活剂(RANKL)进一步促进了这一过程。对 BMM 施加力会加速 TNF-α诱导的破骨细胞形成;这可以通过抗 TNF-α或抗 TNF-α受体抑制,但不能通过 OPG 抑制。TNF-α还在 BMM 中增加 c-Fms 的 mRNA 和蛋白水平表达。抗 c-Fms 抗体完全抑制了 TNF-α诱导的破骨细胞分化和骨吸收,但部分阻断了与 RANKL 联合刺激的破骨细胞形成。这些结果表明,TNF-α(在 M-CSF 存在的情况下)能够诱导 BMM 中的破骨细胞形成,并且通过激活 c-Fms 介导的信号,力的施加会显著刺激破骨细胞形成。总体而言,本研究揭示了机械力在没有添加机械敏感细胞的情况下促进 BMM 中破骨细胞分化的作用。

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