Emodin Regulates Bone Remodeling by Inhibiting Osteoclastogenesis and Stimulating Osteoblast Formation

被引:79
作者
Kim, Ju-Young [1 ]
Cheon, Yoon-Hee [2 ,3 ,4 ]
Kwak, Sung Chul [2 ,3 ,4 ]
Baek, Jong Min [2 ,3 ,4 ]
Yoon, Kwon-Ha [1 ,5 ]
Lee, Myeung Su [1 ,2 ,6 ]
Oh, Jaemin [1 ,2 ,3 ,4 ,6 ,7 ]
机构
[1] Wonkwang Univ, Imaging Sci Based Lung & Bone Dis Res Ctr, Iksan 570749, Jeonbuk, South Korea
[2] Wonkwang Univ, Sch Med, Dept Anat, Iksan 570749, Jeonbuk, South Korea
[3] Wonkwang Univ, Program BK21Plus, Iksan 570749, Jeonbuk, South Korea
[4] Wonkwang Univ, Grad Sch, Dept Smart Life Care Convergence, Iksan 570749, Jeonbuk, South Korea
[5] Wonkwang Univ, Sch Med, Dept Radiol, Iksan 570749, Jeonbuk, South Korea
[6] Wonkwang Univ, Inst Skeletal Dis, Iksan 570749, Jeonbuk, South Korea
[7] Wonkwang Univ, Dept Internal Med, Div Rheumatol, Iksan 570749, Jeonbuk, South Korea
关键词
BONE REMODELING; EMODIN; OSTEOBLAST; OSTEOCLAST; OSTEOPOROSIS; NF-KAPPA-B; RETRACTED ARTICLE. SEE; P2X(7) RECEPTOR; P2X7; RECEPTORS; TRANSCRIPTION FACTORS; LIGAND RANKL; IN-VITRO; DIFFERENTIATION; ACTIVATION; EXPRESSION;
D O I
10.1002/jbmr.2183
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone remodeling, a physiological process in which new bone is formed by osteoblasts and the preexisting bone matrix is resorbed by osteoclasts, is vital for the maintenance of healthy bone tissue in adult humans. Imbalances in this process can cause various pathological conditions, including osteoporosis. Emodin, a naturally occurring anthraquinone derivative found in Asian herbal medicines, has numerous beneficial pharmacologic effects, including anticancer and antidiabetic activities. However, the effect of emodin on the regulation of osteoblast and osteoclast activity has not yet been investigated. We show here that emodin is a potential target for osteoporosis therapeutics, as treatment with this agent enhances osteoblast differentiation and bone growth and suppresses osteoclast differentiation and bone resorption. In this study, emodin suppressed receptor activator of nuclear factor-kappa B (NF-kappa B) ligand (RANKL)-induced osteoclast differentiation of bone marrow macrophages (BMMs) and the bone-resorbing activity of mature osteoclasts by inhibiting RANKL-induced NF-kappa B, c-Fos, and NFATc1 expression. Emodin also increased ALP, Alizarin Red-mineralization activity, and the expression of osteoblastogenic genemarkers, such as Runx2, osteocalcin (OCN), and ALP in mouse calvarial primary osteoblasts, as well as activated the p38-Runx2 pathway, which enhanced osteoblast differentiation. Moreover, mice treated with emodin showed marked attenuation of lipopolysaccharide (LPS)-induced bone erosion and increased bone-forming activity in a mouse calvarial bone formation model based on micro-computed tomography and histologic analysis of femurs. Our findings reveal a novel function for emodin in bone remodeling, and highlight its potential for use as a therapeutic agent in the treatment of osteoporosis that promotes bone anabolic activity and inhibits osteoclast differentiation. (C) 2014 American Society for Bone and Mineral Research.
引用
收藏
页码:1541 / 1553
页数:13
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