Department of Orthopaedics, The Fourth Affiliated Hospital of Harbin Medical University, 150006, Harbin, China.
Department of Orthopaedics, The Fourth Affiliated Hospital of Harbin Medical University, 150006, Harbin, China.
Biochem Biophys Res Commun. 2020 Aug 27;529(3):629-634. doi: 10.1016/j.bbrc.2020.05.192. Epub 2020 Jul 17.
Periprosthetic osteolysis (PIO) caused by wear particles is the main cause of implant failure, which is regulated by nuclear factor κ B receptor activator ligand (RANKL)/osteoprotegerin (OPG) system. At present, there is a lack of effective drugs to prevent or treat PIO. Previous studies have confirmed that DNA methylation is closely related to postmenopausal osteoporosis and can affect the expression of OPG and RANKL. However, the relationship between DNA methylation and PIO is not clear. In this study, we investigated the inhibitory effect of 5-Aza-2-deoxycytidine (AzadC) on osteolysis induced by titanium particles in a mouse model. This inhibition mechanism is achieved by changing the ratio of RANKL/OPG in the osteolysis model. In conclusion, there is a relationship between DNA methylation and PIO. AzadC has a certain inhibitory effect on osteolysis induced by titanium particles. Regulating DNA methylation may be a new way to treat PIO. Our findings lay a foundation for epigenetic understanding and intervention of osteolysis.
假体周围骨溶解(PIO)是由磨损颗粒引起的,是导致植入物失效的主要原因,其受核因子 κ B 受体激活配体(RANKL)/骨保护素(OPG)系统调控。目前,缺乏有效的药物来预防或治疗 PIO。先前的研究已经证实,DNA 甲基化与绝经后骨质疏松症密切相关,可影响 OPG 和 RANKL 的表达。然而,DNA 甲基化与 PIO 的关系尚不清楚。在本研究中,我们研究了 5-氮杂-2-脱氧胞苷(AzadC)对小鼠模型中钛颗粒诱导的溶骨的抑制作用。这种抑制机制是通过改变溶骨模型中 RANKL/OPG 的比值来实现的。总之,DNA 甲基化与 PIO 之间存在一定的关系。AzadC 对钛颗粒诱导的溶骨具有一定的抑制作用。调节 DNA 甲基化可能是治疗 PIO 的一种新方法。我们的研究结果为骨溶解的表观遗传学理解和干预奠定了基础。