Department of Orthopaedic Surgery, Shengzhou People's Hospital (the First Affiliated Hospital of Zhejiang University Shengzhou Branch), Shaoxing, 312000, Zhejiang, China.
Department of Orthopaedic Surgery, Huating First People's Hospital, Pingliang, 744000, Gansu, China.
Calcif Tissue Int. 2022 Aug;111(2):211-223. doi: 10.1007/s00223-022-00980-2. Epub 2022 May 19.
Aseptic loosening of the prosthesis caused by wear-particle-induced osteolysis is a long-term complication and one of the most common reasons for the failure of joint implants. The primary cause of aseptic loosening of the prosthesis is overactive bone resorption caused by wear-particle-activated osteoclasts in both direct and indirect ways. Therefore, drugs that can inhibit differentiation and bone resorption of osteoclasts need investigation as a potential therapeutic strategy to prevent and treat peri-prosthetic osteolysis and thereby prolong the service life of the prosthesis. This study has verified the potential inhibitory effect of LY450139 on inflammatory osteolysis induced by titanium particles in a mice skull model. In addition, we found that LY450139 inhibited receptor activator of NF-κB ligand (RANKL)-induced osteoclastogenesis, bone resorption, and podosomal actin belt formation in a dose-dependent manner without evidence of cytotoxicity in vitro. In addition, LY450139 significantly decreased the expression of osteoclast-specific markers, including TRAP, CTSK, V-ATPase d2, CTR, DC-STAMP, NFATc1, and the downstream target gene Hes1 in Notch signaling pathway. Further investigation of the molecular mechanism demonstrated that LY450139 inhibited the formation of osteoclasts via inhibition of the NF-κB and Notch signaling pathways. In summary, LY450139 inhibited the formation of RANKL-mediated osteoclasts via NF-κB and Notch signaling and inhibited Ti particle-induced inflammatory osteolysis in vivo. LY450139 is a potential targeted drug for the treatment of peri-prosthetic osteolysis and other osteolytic disease associated with overactive osteoclasts.
假体无菌性松动是由磨损颗粒诱导的骨溶解引起的一种长期并发症,也是关节植入物失效的最常见原因之一。假体无菌性松动的主要原因是磨损颗粒激活的破骨细胞通过直接和间接途径引起的过度骨吸收。因此,需要研究能够抑制破骨细胞分化和骨吸收的药物,作为一种潜在的治疗策略,以预防和治疗假体周围骨溶解,从而延长假体的使用寿命。本研究已验证 LY450139 对钛颗粒诱导的小鼠颅骨模型炎症性骨溶解的潜在抑制作用。此外,我们发现 LY450139 可抑制核因子-κB 受体激活配体(RANKL)诱导的破骨细胞生成、骨吸收和破骨细胞足突带形成,且体外无细胞毒性。此外,LY450139 可显著降低破骨细胞特异性标志物的表达,包括 TRAP、CTSK、V-ATPase d2、CTR、DC-STAMP、NFATc1 和 Notch 信号通路中的下游靶基因 Hes1。进一步的分子机制研究表明,LY450139 通过抑制 NF-κB 和 Notch 信号通路抑制破骨细胞的形成。综上所述,LY450139 通过 NF-κB 和 Notch 信号通路抑制 RANKL 介导的破骨细胞形成,并抑制体内 Ti 颗粒诱导的炎症性骨溶解。LY450139 是一种潜在的治疗假体周围骨溶解和其他与过度活跃的破骨细胞相关的溶骨性疾病的靶向药物。