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Erschienen in: Clinical Oral Investigations 6/2014

01.07.2014 | Original Article

TGF-βRI kinase activity mediates Emdogain-stimulated in vitro osteoclastogenesis

verfasst von: Reinhard Gruber, Gilles Roos, Jordi Caballé-Serrano, Rick Miron, Dieter D. Bosshardt, Anton Sculean

Erschienen in: Clinical Oral Investigations | Ausgabe 6/2014

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Abstract

Objectives

Emdogain, containing an extract of fetal porcine enamel matrix proteins, is a potent stimulator of in vitro osteoclastogenesis. The underlying molecular mechanisms are, however, unclear.

Material and methods

Here, we have addressed the role of transforming growth factor-beta receptor type 1 (TGF-βRI) kinase activity on osteoclastogenesis in murine bone marrow cultures.

Results

Inhibition of TGF-βRI kinase activity with SB431542 abolished the effect of Emdogain on osteoclastogenesis induced by receptor activator of nuclear factor kappa-B ligand or tumor necrosis factor-alpha. SB431542 also suppressed the Emdogain-mediated increase of OSCAR, a co-stimulatory protein, and dendritic cell-specific transmembrane protein and Atp6v0d2, the latter two being involved in cell fusion. Similar to transforming growth factor-beta1 (TGF-β), Emdogain could not compensate for the inhibition of IL-4 and IFNγ on osteoclast formation. When using the murine macrophage cell line RAW246.7, SB431542 and the smad-3 inhibitor SIS3 blocked Emdogain-stimulated expression of the transcription factor NFATc1.

Conclusions

Taken together, the data suggest that TGF-βRI kinase activity is necessary to mediate in vitro effects of Emdogain on osteoclastogenesis.

Clinical relevance

Based on these in vitro data, we can speculate that at least part of the clinical effects of Emdogain on osteoclastogenesis is mediated via TGF-β signaling.
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Metadaten
Titel
TGF-βRI kinase activity mediates Emdogain-stimulated in vitro osteoclastogenesis
verfasst von
Reinhard Gruber
Gilles Roos
Jordi Caballé-Serrano
Rick Miron
Dieter D. Bosshardt
Anton Sculean
Publikationsdatum
01.07.2014
Verlag
Springer Berlin Heidelberg
Erschienen in
Clinical Oral Investigations / Ausgabe 6/2014
Print ISSN: 1432-6981
Elektronische ISSN: 1436-3771
DOI
https://doi.org/10.1007/s00784-013-1129-6

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