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The coffee diterpene kahweol prevents osteoclastogenesis via impairment of NFATc1 expression and blocking of Erk phosphorylation
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نویسنده
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fumimoto r. ,sakai e. ,yamaguchi y. ,sakamoto h. ,fukuma y. ,nishishita k. ,okamoto k. ,tsukuba t.
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منبع
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journal of pharmacological sciences - 2012 - دوره : 118 - شماره : 4 - صفحه:479 -486
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چکیده
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Osteoclasts (ocls) are multinucleated bone resorbing cells whose differentiation is regulated by receptor activator of nuclear factor kappa-b ligand (rankl) and macrophage colony-stimulating factor (m-csf). it is known that inflammatory cytokines and oxidative stress stimulate differentiation of ocls. here we evaluated the effects of kahweol,a coffee-specific diterpene,which has been reported to possess anti-oxidant and anti-inflammatory properties,on the differentiation of bone marrow-derived macrophages (bmms) or murine monocytic cell line raw-d cells into ocls. kahweol dose-dependently inhibited the formation of tartrate-resistant acid phosphatase staining-positive ocls from both bmms and raw-d cells. in addition,kahweol prevented the bone resorbing activity of ocls. kahweol completely abolished rankl-stimulated phosphorylation of extracellular signal-regulated kinase and impaired phosphorylation of akt. moreover,the protein levels of nuclear factor of activated t cells cytoplasmic-1 (nfatc1),a master regulator for ocl differentiation; and ocl markers transcriptionally regulated by nfatc1 such as src and cathepsin k were down-regulated by kahweol treatment. as one of the molecular mechanisms for the inhibitory effects of kahweol,we also showed that kahweol up-regulated heme oxygenase-1 and inhibited high mobility group box 1 release. thus,kahweol in coffee is a useful constituent for inhibition of ocl differentiation. © the japanese pharmacological society.
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کلیدواژه
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Extracellular signal-regulated kinase (Erk); Kahweol; Nuclear factor of activated T cells cytoplasmic-1 (NFATc1); Osteoclast; Receptor activator of nuclear factor kappa-B ligand (RANKL)
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آدرس
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division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan, division of oral pathopharmacology,nagasaki university,graduate school of biomedical sciences,1-7-1 sakamoto,nagasaki 852-8588, Japan
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Authors
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