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正硅酸抑制 RANKL 诱导的破骨细胞生成并逆转体内去卵巢诱导的骨丢失。

Ortho-silicic Acid Inhibits RANKL-Induced Osteoclastogenesis and Reverses Ovariectomy-Induced Bone Loss In Vivo.

机构信息

Department of Spine Surgery, Qilu Hospital of Shandong University, Jinan, China.

Department of traumatic Orthopedics, West Branch of Shandong Provincial Hospital, Jinan, China.

出版信息

Biol Trace Elem Res. 2021 May;199(5):1864-1876. doi: 10.1007/s12011-020-02286-6. Epub 2020 Jul 16.

Abstract

Numerous experiments in vitro and in vivo have shown that an appropriate increase intake of silicon can facilitate the synthesis of collagen and its stabilization and promote the differentiation and mineralization of osteoblasts. In this study, we examined whether ortho-silicic acid restrains the differentiation of osteoclast through the receptor activator of nuclear factor κB ligand (RANKL)/receptor activator of nuclear factor κB (RANK)/osteoprotegerin (OPG) signaling pathway by investigating its effect in vitro and in vivo. Bone marrow macrophage (BMM) cells were isolated and cultured with or without ortho-silicic acid, and then TRAP staining and immunofluorescence were performed to detect the differentiation of osteoclast. The RANKL-induced osteoclast marker gene and protein expression including c-Fos, nuclear factor of activated T cells cl (NFATcl), tumor necrosis factor receptor-associated factor 6 (TRAF6), nuclear factor kappa B P50 (NF-κB P50), NF-κB P52, RANK, integrin β3, cathepsin K (CTSK), DC-STAMP, and TRAP were quantitatively detected by western blot and RT-PCR. Ovariectomized (OVX) rats were injected with ortho-silicic acid (OVX+Si group) and normal saline (OVX group), and sham-operated rats were injected with normal saline (Sham group). And micro-CT, H&E, and TRAP staining, ELISA, and western blot were performed. Ortho-silicic acid could inhibit the differentiation of osteoclast, and the marker genes and proteins were decreased. The OVX-induced bone loss could be reversed by ortho-silicic acid. Our finding demonstrated that ortho-silicic acid suppresses RANKL-induced osteoclastogenesis and has potential value as a therapeutic agent for OVX-induced bone loss.

摘要

大量的体外和体内实验表明,适当增加硅的摄入可以促进胶原蛋白的合成及其稳定,并促进成骨细胞的分化和矿化。在这项研究中,我们通过研究其在体外和体内的作用,来检验正硅酸是否通过核因子κB 受体激活剂配体(RANKL)/核因子κB 受体激活剂(RANK)/骨保护素(OPG)信号通路来抑制破骨细胞的分化。分离和培养骨髓巨噬细胞(BMM)细胞,用或不用正硅酸,然后进行 TRAP 染色和免疫荧光检测破骨细胞的分化。通过 Western blot 和 RT-PCR 定量检测 RANKL 诱导的破骨细胞标记基因和蛋白的表达,包括 c-Fos、激活 T 细胞核因子 cl(NFATcl)、肿瘤坏死因子受体相关因子 6(TRAF6)、核因子κB P50(NF-κB P50)、NF-κB P52、RANK、整合素β3、组织蛋白酶 K(CTSK)、DC-STAMP 和 TRAP。去卵巢(OVX)大鼠注射正硅酸(OVX+Si 组)和生理盐水(OVX 组),假手术大鼠注射生理盐水(Sham 组)。并进行微 CT、H&E 和 TRAP 染色、ELISA 和 Western blot。正硅酸可以抑制破骨细胞的分化,标记基因和蛋白的表达减少。正硅酸可以逆转 OVX 诱导的骨丢失。我们的发现表明,正硅酸抑制 RANKL 诱导的破骨细胞生成,具有作为 OVX 诱导的骨丢失治疗剂的潜在价值。

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