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Mechanism of osteogenic induction by FK506 via BMP/Smad pathways.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2005 Dec 16; Vol. 338 (2), pp. 872-9. Date of Electronic Publication: 2005 Oct 14. - Publication Year :
- 2005
-
Abstract
- FK506 is an immunosuppressant that exerts effects by binding to FK506-binding protein 12 (FKBP12). Recently, FK506 has also been reported to promote osteogenic differentiation when administered locally or in vitro in combination with bone morphogenetic proteins (BMPs), although the underlying mechanism remains unclarified. The present study initially showed that FK506 alone at a higher concentration (1muM) induced osteogenic differentiation of mesenchymal cell lines, which was suppressed by adenoviral introduction of Smad6. FK506 rapidly activates the BMP-dependent Smads in the absence of BMPs, and the activation was blocked by Smad6. Overexpression of FKBP12, which was reported to block the ligand-independent activation of BMP type I receptor A (BMPRIA), suppressed Smad signaling induced by FK506, but not that induced by BMP2. BMPRIA and FKBP12 bound to each other, and this binding was suppressed by FK506. These data suggest that FK506 promotes osteogenic differentiation by activating BMP receptors through interacting with FKBP12.
- Subjects :
- Animals
Cell Differentiation drug effects
Cell Differentiation physiology
Cell Line
Dose-Response Relationship, Drug
Gene Expression Regulation drug effects
Gene Expression Regulation physiology
Mesenchymal Stem Cells drug effects
Mice
Osteogenesis drug effects
Signal Transduction drug effects
Bone Morphogenetic Proteins metabolism
Mesenchymal Stem Cells cytology
Mesenchymal Stem Cells physiology
Osteogenesis physiology
Signal Transduction physiology
Smad Proteins metabolism
Tacrolimus administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 338
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 16246307
- Full Text :
- https://doi.org/10.1016/j.bbrc.2005.10.024