Disclosure of potential conflicts of interest is found at the end of this article.
Embryonic Stem Cells/Induced Pluripotent Stem Cells
Article first published online: 2 MAR 2009
Copyright © 2009 AlphaMed Press
Volume 27, Issue 3, pages 550–558, March 2009
How to Cite
Duque, G., Huang, D. C., Macoritto, M., Rivas, D., Yang, X. F., Ste-Marie, L. G. and Kremer, R. (2009), Autocrine Regulation of Interferon γ in Mesenchymal Stem Cells Plays a Role in Early Osteoblastogenesis. STEM CELLS, 27: 550–558. doi: 10.1634/stemcells.2008-0886
Author contributions: G.D.: conception and design, collection and assembly of data, data analysis and interpretation, manuscript writing; D.C.H.: collection and assembly of data, data analysis; G.D. and D.C.H. contributed equally to the manuscript; L.G.S.M.: data analysis and interpretation, manuscript writing; R.K.: conception and design, collection and assembly of data, data analysis and interpretation, manuscript writing; M.M.: collection and assembly of data, data analysis and interpretation; D.R.: collection and assembly of data, data analysis; X.F.Y.: collection and assembly of data, data analysis.
First published online in STEM CELLSExpress December 18, 2008.
- Issue published online: 2 MAR 2009
- Article first published online: 2 MAR 2009
- Manuscript Accepted: 9 DEC 2008
- Manuscript Received: 8 SEP 2008
- Bone turnover;
- Mesenchymal stem cells;
- Interferon gamma;
Interferon (IFN)γ is a strong inhibitor of osteoclast differentiation and activity. However, its role in osteoblastogenesis has not been carefully examined. Using microarray expression analysis, we found that several IFNγ-inducible genes were upregulated during early phases of osteoblast differentiation of human mesenchymal stem cells (hMSCs). We therefore hypothesized that IFNγ may play a role in this process. We first observed a strong and transient increase in IFNγ production following hMSC induction to differentiate into osteoblasts. We next blocked this endogenous production using a knockdown approach with small interfering RNA and observed a strong inhibition of hMSC differentiation into osteoblasts with a concomitant decrease in Runx2, a factor indispensable for osteoblast development. Additionally, exogenous addition of IFNγ accelerated hMSC differentiation into osteoblasts in a dose-dependent manner and induced higher levels of Runx2 expression during the early phase of differentiation. We next examined IFNγ signaling in vivo in IFNγ receptor 1 knockout (IFNγR1−/−) mice. Compared with their wild-type littermates, IFNγR1−/− mice exhibited a reduction in bone mineral density. As in the in vitro experiments, MSCs obtained from IFNγR1−/− mice showed a lower capacity to differentiate into osteoblasts. In summary, we demonstrate that the presence of IFNγ plays an important role during the commitment of MSCs into the osteoblastic lineage both in vitro and in vivo, and that this process can be accelerated by exogenous addition of IFNγ. These data therefore support a new role for IFNγ as an autocrine regulator of hMSC differentiation and as a potential new target of bone-forming cells in vivo. STEM CELLS2009;27:550–558