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Experimental & Molecular Medicine ; : 437-445, 2010.
Article Dans Anglais | WPRIM | ID: wpr-27759

Résumé

TNF-alpha, a proinflammatory cytokine, inhibits osteoblast differentiation under diverse inflammatory conditions; however, the underlying mechanisms in terms of the TNF-alpha signaling pathway remain unclear. In this study, we examined the role of Msx2 in TNF-alpha-mediated inhibition of alkaline phosphatase (ALP) expression and the signaling pathways involved. TNF-alpha down-regulated ALP expression induced by bone morphogenetic protein 2 (BMP2) in C2C12 and Runx2-/- calvarial cells. Over-expression of Msx2 suppressed BMP2-induced ALP expression. Furthermore, TNF-alpha induced Msx2 expression, and the knockdown of Msx2 by small interfering RNAs rescued ALP expression, which was inhibited by TNF-alpha. TNF-alpha activated the NF-kappaB and the JNK pathways. Inhibition of NF-kappaB or JNK activation reduced the inhibitory effect of TNF-alpha on ALP expression, whereas TNF-alpha-induced Msx2 expression was only suppressed by the inhibition of the NF-kappaB pathway. Taken together, these results indicate that Msx2 mediates the inhibitory action of TNF-alpha on BMP2-regulated osteoblast differentiation and that the TNF-alpha-activated NF-kappaB pathway is responsible for Msx2 induction.


Sujets)
Animaux , Souris , Phosphatase alcaline/génétique , Animaux nouveau-nés , Protéine morphogénétique osseuse de type 2/pharmacologie , Techniques de culture cellulaire , Différenciation cellulaire/effets des médicaments et des substances chimiques , Prolifération cellulaire/effets des médicaments et des substances chimiques , Cellules cultivées , Sous-unité alpha 1 du facteur CBF/génétique , Régulation négative/effets des médicaments et des substances chimiques , Régulation de l'expression des gènes/effets des médicaments et des substances chimiques , Protéines à homéodomaine/antagonistes et inhibiteurs , Souris de lignée ICR , Souris transgéniques , Ostéoblastes/effets des médicaments et des substances chimiques , Petit ARN interférent/pharmacologie , Facteur de nécrose tumorale alpha/pharmacologie
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