Attenuation of osteoclastogenesis and osteoclast function by apigenin

被引:80
作者
Bandyopadhyay, Sanghamitra
Lion, Jean-Marc
Mentaverri, Romuald
Ricupero, Dennis A.
Kamel, Said
Romero, Jose R.
Chattopadhyay, Naibedya
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Psychiat,Genet & Aging Res Unit, Charlestown, MA 02129 USA
[3] Fac Pharm, Unite Etude Mecan Resorpt Osseuse, F-80037 Amiens, France
[4] Fac Pharm, INSERM, F-80037 Amiens, France
关键词
flavonoids; bone resorption; osteoporosis; rheumatic arthritis; tumor necrosis factor; interferon gamma;
D O I
10.1016/j.bcp.2006.04.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The physiological effects of the flavone, apigenin on bone cells were studied. We first show that apigenin inhibits tumor necrosis factor alpha (TNF alpha)- and interferon gamma (IFN gamma)-induced secretion of several osteoclastogenic cytokines from MC3T3-E1 mouse calvarial osteoblast cell line. Ligands of the TNT receptor family constitute the most potent osteoclastic cytokines. In MC3T3-E1 cells, apigenin dose-dependently (from 5 to 20 mu M) inhibits TNF alpha-induced production of the osteoclastogenic cytokines, IL-6 (interleukin-6), RANTES (regulated upon activation, normal T cell-expressed and -secreted), monocyte chemoattractant protein-1 (MCP-1) and MCP-3. In addition, apigenin inhibits IFN gamma-stimulated secretion of monokines, CXCL-9, and -10 in MC3T3-E1 cells. Next, we show that apigenin strongly inhibits differentiation of 3T3-L1 preadipocytes to adipocytes with attendant inhibition of adipocyte differentiation -induced IL-6, MCP-1, and leptin production. Inhibition of adipogenic differentiation by apigenin could be due to induction of osteogensis as it robustly upregulates mRNA levels of bone morphogenetic protein-6 (BMP-6). Finally, the presence of apigenin inhibited osteoclast differentiation from the RAW 264.7 cell line by reducing receptor activator of nuclear factor kappa ligand (RANKL)-induced expression of tartrate-resistant acid phosphatase (TRAP), RANK, and calcitonin receptor but not CCR1, resulting in the inhibition of multinucleated osteoclast formation. Similarly, apigenin inhibited expression of the osteoclast differentiation markers TRAP, RANK, and c-Fms in osteoclast precursor cells obtained from mouse bone marrow following treatment with RANKL and macrophage colony stimulating factor (MCSF). Furthermore, apigenin induced apoptosis of mature osteoclasts obtained from rabbit long bone and inhibited bone resorption. In all instances, a structurally related compound, flavone had no significant effect. These data suggest that apigenin has multiple effects on all three bone cells that could prevent bone loss in vivo. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:184 / 197
页数:14
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