Suppr超能文献

干细胞再生因子1通过抑制芳烃受体--Src-核因子κB/磷酸化细胞外信号调节激酶丝裂原活化蛋白激酶-活化T细胞核因子c1信号通路来减弱核因子κB受体活化因子配体诱导的破骨细胞生成。

StemRegenin 1 attenuates the RANKL-induced osteoclastogenesis via inhibiting AhR--src-NF-κB/p-ERK MAPK-NFATc1 signaling pathway.

作者信息

Zhou Shengji, Li Jiarui, Ying Tiantian, Wang Yuxin, Wang Quan, Li Xiang, Zhao Fengchao

机构信息

Department of Orthopaedic Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, P.R. China.

出版信息

iScience. 2024 Apr 6;27(5):109682. doi: 10.1016/j.isci.2024.109682. eCollection 2024 May 17.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/885e/11039397/170663f5e312/fx1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验