Qi Wenting, Gao Yan, Tian Jun, Jiang Hongwei
Department of Operative Dentistry and Endodontics, Guanghua School and Hospital of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Sun Yat‑sen University, Guangzhou, Guangdong 510055, P.R. China.
Int J Mol Med. 2014 Dec;34(6):1483-91. doi: 10.3892/ijmm.2014.1941. Epub 2014 Sep 22.
Osteoclastogenesis is a complex process that is highly dependent on the dynamic regulation of the actin cytoskeleton. Adseverin (Ads), a member of the gelsolin superfamily of actin-binding proteins, regulates actin remodeling by severing and capping actin filaments. The objective of the present study was to characterize the role of Ads during osteoclastogenesis by assessing Ads expression and using a knockdown strategy. Immunoblot analyses were used to examine Ads expression during osteoclastogenesis. A stable Ads knockdown macrophage cell line was generated using a retroviral shRNA construct. Osteoclast differentiation was morphologically examined via cell staining with osteoclast specific markers and light microscopy. The results showed that Ads expression was significantly increased in response to receptor activator of nuclear factor-κB ligand during osteoclastogenesis, and Ads was highly expressed in mature osteoclasts. Ads-knockdown macrophages showed major osteoclastogenesis defects, most likely caused by a pre-osteoclast fusion defect. These results indicate that Ads deficiency in monocytes inhibits osteoclastogenesis. Thus, in future studies it could be noteworthy to investigate the function of Ads in bone marrow monocytes during osteoclastogenesis.
破骨细胞生成是一个复杂的过程,高度依赖于肌动蛋白细胞骨架的动态调节。Adseverin(Ads)是肌动蛋白结合蛋白凝溶胶蛋白超家族的成员,通过切断和封端肌动蛋白丝来调节肌动蛋白重塑。本研究的目的是通过评估Ads表达并采用敲低策略来表征Ads在破骨细胞生成过程中的作用。免疫印迹分析用于检测破骨细胞生成过程中Ads的表达。使用逆转录病毒shRNA构建体生成稳定的Ads敲低巨噬细胞系。通过用破骨细胞特异性标记物进行细胞染色和光学显微镜对破骨细胞分化进行形态学检查。结果表明,在破骨细胞生成过程中,Ads的表达响应核因子-κB受体激活剂配体而显著增加,并且Ads在成熟破骨细胞中高表达。Ads敲低的巨噬细胞表现出主要的破骨细胞生成缺陷,最可能是由破骨前体细胞融合缺陷引起的。这些结果表明单核细胞中Ads的缺乏会抑制破骨细胞生成。因此,在未来的研究中,研究Ads在破骨细胞生成过程中在骨髓单核细胞中的功能可能是值得关注的。