Chen Yueqi, Hu Wenhui, Wang Yiran, Li Yuheng, Li Xiaoming, Li Haibo, Tang Yong, Zhang Lincheng, Dong Yutong, Yang Xiaochao, Wei Ye, Dong Shiwu
Department of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Department of Orthopaedics, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, PR China.
Clin Transl Med. 2020 Dec;10(8):e240. doi: 10.1002/ctm2.240.
Inflammatory osteolysis is a severe infectious bone disorder that occurs during orthopaedic surgery and is caused by disruptions in the dynamic balance of bone matrix homeostasis, which makes this condition a burden on surgical procedures. Developing novel therapeutic drugs about inhibiting excessive osteoclastogenesis acts as an efficient approach to preventing inflammatory bone destruction.
To study this, we explored the potential effects and mechanisms of compound 17 on inflammatory osteolysis in vitro. Meanwhile, a lipopolysaccharide (LPS)-induced calvarial osteolysis mouse model was used to evaluate the protective effect of compound 17 on inflammatory bone destruction in vivo.
In our study, we found that compound 17 could inhibit osteoclast (OC) differentiation and bone resorption during RANKL and LPS stimulation in a time- and dose-dependent manner, while compounds 5 and 13 did not have the same effects. Mechanistically, compound 17 promoted phosphatase and tensin homologue (PTEN) activity by reducing PTEN ubiquitination, thereby restraining the RANKL-induced NF-κB pathway, resulting in the inhibition of the expression of osteoclastogenesis-related genes and the formation of the NLRP3 inflammasome. Additionally, we also investigated whether compound 17 could negatively modulate macrophage polarization and repolarization due to its anti-inflammatory effects. Moreover, compound 17 also plays an important role in osteoblast differentiation and mineralization. In vivo experiments showed that compound 17 could effectively protect mice from LPS-induced inflammatory bone destruction by inhibiting osteoclastogenesis and inflammation.
Taken together, these results show that compound 17 might play protective role in inflammatory bone destruction through inhibiting osteoclastogenesis and inflammation. These findings imply a possible role of compound 17 in inflammatory osteolysis-related diseases.
炎性骨溶解是一种严重的感染性骨疾病,发生于骨科手术期间,由骨基质稳态动态平衡的破坏所致,这使得这种情况成为手术过程中的一个负担。开发抑制破骨细胞过度生成的新型治疗药物是预防炎性骨破坏的有效方法。
为研究此问题,我们在体外探究了化合物17对炎性骨溶解的潜在作用及机制。同时,使用脂多糖(LPS)诱导的颅骨溶解小鼠模型在体内评估化合物17对炎性骨破坏的保护作用。
在我们的研究中,发现化合物17能在RANKL和LPS刺激期间以时间和剂量依赖性方式抑制破骨细胞(OC)分化和骨吸收,而化合物5和13则没有相同效果。机制上,化合物17通过减少PTEN泛素化来促进磷酸酶和张力蛋白同源物(PTEN)活性,从而抑制RANKL诱导的NF-κB途径,导致破骨细胞生成相关基因的表达受到抑制以及NLRP3炎性小体的形成受到抑制。此外,我们还研究了化合物17是否因其抗炎作用而对巨噬细胞极化和再极化产生负调节作用。而且,化合物17在成骨细胞分化和矿化中也起重要作用。体内实验表明,化合物17可通过抑制破骨细胞生成和炎症有效保护小鼠免受LPS诱导的炎性骨破坏。
综上所述,这些结果表明化合物17可能通过抑制破骨细胞生成和炎症在炎性骨破坏中发挥保护作用。这些发现暗示了化合物17在炎性骨溶解相关疾病中的可能作用。