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愈创木酚通过阻断RANK与TRAF6和C-Src的相互作用以及抑制NF-κB、MAPK和AKT信号通路来抑制破骨细胞生成。

Guaiacol suppresses osteoclastogenesis by blocking interactions of RANK with TRAF6 and C-Src and inhibiting NF-κB, MAPK and AKT pathways.

作者信息

Zhi Xin, Fang Chao, Gu Yanqiu, Chen Huiwen, Chen Xiaofei, Cui Jin, Hu Yan, Weng Weizong, Zhou Qirong, Wang Yajun, Wang Yao, Jiang Hao, Li Xiaoqun, Cao Liehu, Chen Xiao, Su Jiacan

机构信息

Department of Orthopedics Trauma, Shanghai Changhai Hospital, Naval Military Medical University, Shanghai, China.

Basic Medical School, Naval Military Medical University, Shanghai, China.

出版信息

J Cell Mol Med. 2020 May;24(9):5122-5134. doi: 10.1111/jcmm.15153. Epub 2020 Mar 17.

DOI:10.1111/jcmm.15153
PMID:32185887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7205840/
Abstract

Angelica sinensis (AS; Dang Gui), a traditional Chinese herb, has for centuries been used for the treatment of bone diseases, including osteoporosis and osteonecrosis. However, the effective ingredient and underlying mechanisms remain elusive. Here, we identified guaiacol as the active component of AS by two-dimensional cell membrane chromatography/C18 column/time-of-flight mass spectrometry (2D CMC/C18 column/TOFMS). Guaiacol suppressed osteoclastogenesis and osteoclast function in bone marrow monocytes (BMMCs) and RAW264.7 cells in vitro in a dose-dependent manner. Co-immunoprecipitation indicated that guaiacol blocked RANK-TRAF6 association and RANK-C-Src association. Moreover, guaiacol prevented phosphorylation of p65, p50, IκB (NF-κB pathway), ERK, JNK, c-fos, p38 (MAPK pathway) and Akt (AKT pathway), and reduced the expression levels of Cathepsin K, CTR, MMP-9 and TRAP. Guaiacol also suppressed the expression of nuclear factor of activated T-cells cytoplasmic 1(NFATc1) and the RANKL-induced Ca oscillation. In vivo, it ameliorated ovariectomy-induced bone loss by suppressing excessive osteoclastogenesis. Taken together, our findings suggest that guaiacol inhibits RANKL-induced osteoclastogenesis by blocking the interactions of RANK with TRAF6 and C-Src, and by suppressing the NF-κB, MAPK and AKT signalling pathways. Therefore, this compound shows therapeutic potential for osteoclastogenesis-related bone diseases, including postmenopausal osteoporosis.

摘要

当归是一种传统中药,几个世纪以来一直用于治疗包括骨质疏松症和骨坏死在内的骨骼疾病。然而,其有效成分和潜在机制仍不清楚。在此,我们通过二维细胞膜色谱/C18柱/飞行时间质谱(2D CMC/C18柱/TOFMS)鉴定出愈创木酚是当归的活性成分。愈创木酚在体外以剂量依赖的方式抑制骨髓单核细胞(BMMCs)和RAW264.7细胞中的破骨细胞生成和破骨细胞功能。免疫共沉淀表明,愈创木酚阻断了RANK与TRAF6的结合以及RANK与C-Src的结合。此外,愈创木酚可阻止p65、p50、IκB(NF-κB途径)、ERK、JNK、c-fos、p38(MAPK途径)和Akt(AKT途径)的磷酸化,并降低组织蛋白酶K、CTR、MMP-9和TRAP的表达水平。愈创木酚还抑制活化T细胞核因子细胞质1(NFATc1)的表达以及RANKL诱导的钙振荡。在体内,它通过抑制过度的破骨细胞生成改善去卵巢诱导的骨质流失。综上所述,我们的研究结果表明,愈创木酚通过阻断RANK与TRAF6和C-Src的相互作用以及抑制NF-κB、MAPK和AKT信号通路来抑制RANKL诱导的破骨细胞生成。因此,这种化合物对包括绝经后骨质疏松症在内的与破骨细胞生成相关的骨骼疾病具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36c0/7205840/0d980d5ea3b4/JCMM-24-5122-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36c0/7205840/12e43a27d3c4/JCMM-24-5122-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36c0/7205840/0d980d5ea3b4/JCMM-24-5122-g008.jpg
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