Guaiacol suppresses osteoclastogenesis by blocking interactions of RANK with TRAF6 and C-Src and inhibiting NF-κB, MAPK and AKT pathways.
Xin ZhiChao FangYanqiu GuHuiwen ChenXiaofei ChenJin CuiYan HuWeizong WengQirong ZhouYajun WangYao WangHao JiangXiaoqun LiLiehu CaoXiao ChenXiaolong LiPublished in: Journal of cellular and molecular medicine (2020)
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 Ca2+ 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.
Keyphrases
- bone loss
- signaling pathway
- induced apoptosis
- pi k akt
- nuclear factor
- high glucose
- diabetic rats
- bone marrow
- cell cycle arrest
- bone mineral density
- poor prognosis
- cell proliferation
- postmenopausal women
- toll like receptor
- oxidative stress
- mass spectrometry
- drug induced
- mesenchymal stem cells
- lps induced
- endothelial cells
- high resolution
- dendritic cells
- immune response
- combination therapy
- cell death
- protein kinase
- tandem mass spectrometry
- long non coding rna
- soft tissue