Zhou Shengji, Li Jiarui, Ying Tiantian, Wang Yuxin, Wang Quan, Li Xiang, Zhao Fengchao
Department of Orthopaedic Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, P.R. China.
iScience. 2024 Apr 6;27(5):109682. doi: 10.1016/j.isci.2024.109682. eCollection 2024 May 17.
The aryl hydrocarbon receptor (AhR) pathway may play an important role in the regulation of osteoclasts, but there are still conflicting studies on this aspect, and the specific mechanism of action has not been fully elucidated. Therefore, we conducted this study to find a drug to treat osteoporosis that targets AhR. We found that StemRegenin 1 inhibited RANKL-induced osteoclastogenesis in a concentration-dependent and time-dependent manner. Through further experiments, we found that SR1 can inhibit nuclear transcription of AhR and inhibit c-src phosphorylation, and ultimately regulates the activation of the NF-κB and -ERK/mitogen-activated protein kinase pathways. Therefore, for the first time, we discovered the way in which the AhR--src-NF-κB/p-ERK MAPK-NFATc1 signaling pathway regulates the expression of osteoclast differentiation-associated proteins. Finally, SR1 was shown to successfully reverse bone loss in OVX mice. These studies provide us with ideas for finding new way to treat osteoporosis.
芳烃受体(AhR)通路可能在破骨细胞的调节中发挥重要作用,但在这方面仍存在相互矛盾的研究,其具体作用机制尚未完全阐明。因此,我们开展了本研究,以寻找一种靶向AhR的治疗骨质疏松症的药物。我们发现,StemRegenin 1以浓度和时间依赖性方式抑制RANKL诱导的破骨细胞生成。通过进一步实验,我们发现SR1可抑制AhR的核转录并抑制c-src磷酸化,最终调节NF-κB和-ERK/丝裂原活化蛋白激酶通路的激活。因此,我们首次发现了AhR--src-NF-κB/p-ERK MAPK-NFATc1信号通路调节破骨细胞分化相关蛋白表达的方式。最后,SR1被证明可成功逆转去卵巢小鼠的骨质流失。这些研究为我们寻找治疗骨质疏松症的新方法提供了思路。