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dc.contributor.authorShakibaei, M.
dc.contributor.authorBuhrmann, C.
dc.contributor.authorMobasheri, A.
dc.date.accessioned2014-04-28T11:20:02Z
dc.date.available2014-04-28T11:20:02Z
dc.date.issued2011
dc.identifier.citationShakibaei, M., Buhrmann, C., Mobasheri, A. (2011) Resveratrol-mediated SIRT-1 interactions with p300 modulate receptor activator of NF-kappaB ligand (RANKL) activation of NF-kappaB signaling and inhibit osteoclastogenesis in bone-derived cells. J Biol Chem, 286 (13), 11492-11505.
dc.identifier.urihttp://hdl.handle.net/10454/6182
dc.description.abstractResveratrol is a polyphenolic phytoestrogen that has been shown to exhibit potent anti-oxidant, anti-inflammatory, and anti-catabolic properties. Increased osteoclastic and decreased osteoblastic activities result in bone resorption and loss of bone mass. These changes have been implicated in pathological processes in rheumatoid arthritis and osteoporosis. Receptor activator of NF-kappaB ligand (RANKL), a member of the TNF superfamily, is a major mediator of bone loss. In this study, we investigated the effects of resveratrol on RANKL during bone morphogenesis in high density bone cultures in vitro. Untreated bone-derived cell cultures produced well organized bone-like structures with a bone-specific matrix. Treatment with RANKL induced formation of tartrate-resistant acid phosphatase-positive multinucleated cells that exhibited morphological features of osteoclasts. RANKL induced NF-kappaB activation, whereas pretreatment with resveratrol completely inhibited this activation and suppressed the activation of IkappaBalpha kinase and IkappaBalpha phosphorylation and degradation. RANKL up-regulated p300 (a histone acetyltransferase) expression, which, in turn, promoted acetylation of NF-kappaB. Resveratrol inhibited RANKL-induced acetylation and nuclear translocation of NF-kappaB in a time- and concentration-dependent manner. In addition, activation of Sirt-1 (a histone deacetylase) by resveratrol induced Sirt-1-p300 association in bone-derived and preosteoblastic cells, leading to deacetylation of RANKL-induced NF-kappaB, inhibition of NF-kappaB transcriptional activation, and osteoclastogenesis. Co-treatment with resveratrol activated the bone transcription factors Cbfa-1 and Sirt-1 and induced the formation of Sirt-1-Cbfa-1 complexes. Overall, these results demonstrate that resveratrol-activated Sirt-1 plays pivotal roles in regulating the balance between the osteoclastic versus osteoblastic activity result in bone formation in vitro thereby highlighting its therapeutic potential for treating osteoporosis and rheumatoid arthritis-related bone loss.
dc.relation.isreferencedbyhttp://dx.doi.org/10.1074/jbc.M110.198713
dc.subjectAnimals;
dc.subjectBone marrow cells; Metabolism;
dc.subjectCell line;
dc.subjectCore binding factor Alpha 1 subunit; Genetics;
dc.subjectDogs;
dc.subjectEnzyme inhibitors; Pharmacology;
dc.subjectHumans;
dc.subjectMice;
dc.subjectMultiprotein complexes;
dc.subjectNF-kappa B;
dc.subjectOsteoclasts;
dc.subjectOsteoporosis; Drug therapy;
dc.subjectRANK Ligand;
dc.subjectRheumatic fever;
dc.subjectSignal transduction; Drug effects;
dc.subjectSirtuin 1;
dc.subjectStilbenes;
dc.subjectUp-regulation;
dc.subjectp300-CBP transcription factors;
dc.subjectREF 2014
dc.titleResveratrol-mediated SIRT-1 interactions with p300 modulate receptor activator of NF-kappaB ligand (RANKL) activation of NF-kappaB signaling and inhibit osteoclastogenesis in bone-derived cells
dc.typeArticle


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