The authors state that they have no conflicts of interest.
20(S)-Hydroxycholesterol Inhibits PPARγ Expression and Adipogenic Differentiation of Bone Marrow Stromal Cells Through a Hedgehog-Dependent Mechanism†
Article first published online: 16 JUL 2007
Copyright © 2007 ASBMR
Journal of Bone and Mineral Research
Volume 22, Issue 11, pages 1711–1719, November 2007
How to Cite
Kim, W.-K., Meliton, V., Amantea, C. M., Hahn, T. J. and Parhami, F. (2007), 20(S)-Hydroxycholesterol Inhibits PPARγ Expression and Adipogenic Differentiation of Bone Marrow Stromal Cells Through a Hedgehog-Dependent Mechanism. J Bone Miner Res, 22: 1711–1719. doi: 10.1359/jbmr.070710
- Issue published online: 4 DEC 2009
- Article first published online: 16 JUL 2007
- Manuscript Accepted: 9 JUL 2007
- Manuscript Revised: 1 JUN 2007
- Manuscript Received: 19 DEC 2006
- mesenchymal stem cells;
- peroxisome proliferator-activated receptor γ;
- CCAAT/enhancer-binding protein α
Specific oxysterols have been shown to be pro-osteogenic and anti-adipogenic. However, the molecular mechanism(s) by which oxysterols inhibit adipogenic differentiation is unknown. We show that the anti-adipogenic effects of osteogenic oxysterol, 20(S)-hydroxycholesterol, are mediated through a hedgehog-dependent mechanism(s) and are associated with inhibition of PPARγ expression.
Introduction: Multipotent bone marrow stromal cells (MSCs) are common progenitors of osteoblasts and adipocytes. A reciprocal relationship between osteogenic and adipogenic differentiation may explain the increased adipocyte and decreased osteoblast formation in aging and osteoporosis. We have previously reported that specific oxysterols stimulate osteogenic differentiation of MSCs while inhibiting their adipogenic differentiation.
Materials and Methods: The M2–10B4 (M2) murine pluripotent bone MSC line was used to assess the inhibitory effects of 20(S)-hydroxycholesterol (20S) and sonic hedgehog (Shh) on peroxisome proliferator-activated receptor γ (PPARγ) and adipogenic differentiation. All results were analyzed for statistical significance using ANOVA.
Results and Conclusions: Treatment of M2 cells with the osteogenic oxysterol 20S completely inhibited adipocyte formation induced by troglitazone after 10 days. PPARγ mRNA expression assessed by RT-qPCR was significantly induced by Tro after 48 (5-fold) and 96 h (130-fold), and this induction was completely inhibited by 20S. In contrast, 20S did not inhibit PPARγ transcriptional activity in M2 cells overexpressing PPARγ and retinoid X receptor (RXR). To elucidate the molecular mechanism(s) by which 20S inhibits PPARγ expression and adipogenic differentiation, we focused on the hedgehog signaling pathway, which we previously showed to be the mediator of osteogenic responses to oxysterols. The hedgehog signaling inhibitor, cyclopamine, reversed the inhibitory effects of 20S and Shh on troglitazone-induced adipocyte formation in 10-day cultures of M2 cells by 70% and 100%, respectively, and the inhibitory effect of 20S and Shh on troglitazone-induced PPARγ expression was fully reversed at 48 h by cyclopamine. Furthermore, 20S and Shh greatly inhibited PPARγ2 promoter activity induced by CCAAT/enhancer-binding protein α overexpression. These studies show that, similar to the induction of osteogenesis, the inhibition of adipogenesis in murine MSCs by the osteogenic oxysterol, 20S, is mediated through a hedgehog-dependent mechanism(s).