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Publication : The crosstalk between transforming growth factor-β1 and delta like-1 mediates early chondrogenesis during embryonic endochondral ossification.

First Author  Taipaleenmäki H Year  2012
Journal  Stem Cells Volume  30
Issue  2 Pages  304-13
PubMed ID  22102178 Mgi Jnum  J:190188
Mgi Id  MGI:5448356 Doi  10.1002/stem.792
Citation  Taipaleenmaki H, et al. (2012) The crosstalk between transforming growth factor-beta1 and delta like-1 mediates early chondrogenesis during embryonic endochondral ossification. Stem Cells 30(2):304-13
abstractText  Delta like-1 (Dlk1)/preadipocyte factor-1 (Pref-1)/fetal antigen-1 (FA1) is a novel surface marker for embryonic chondroprogenitor cells undergoing lineage progression from proliferation to prehypertrophic stages. However, mechanisms mediating control of its expression during chondrogenesis are not known. Thus, we examined the effect of a number of signaling molecules and their inhibitors on Dlk1 expression during in vitro chondrogenic differentiation in mouse embryonic limb bud mesenchymal micromass cultures and mouse embryonic fibroblast (MEF) pellet cultures. Dlk1/Pref-1 was initially expressed during mesenchymal condensation and chondrocyte proliferation, in parallel with expression of Sox9 and Col2a1, and was downregulated upon the expression of Col10a1 by hypertrophic chondrocytes. Among a number of molecules that affected chondrogenesis, transforming growth factor-beta1 (TGF-beta1)-induced proliferation of chondroprogenitors was associated with decreased Dlk1 expression. This effect was abolished by TGF-beta signaling inhibitor SB431542, suggesting regulation of Dlk1/FA1 by TGF-beta1 signaling in chondrogenesis. TGF-beta1-induced Smad phosphorylation and chondrogenesis were significantly increased in Dlk1(-/-) MEF, while they were blocked in Dlk1 overexpressing MEF, in comparison with wild-type MEF. Furthermore, overexpression of Dlk1 or addition of its secreted form FA1 dramatically inhibited TGF-beta1-induced Smad reporter activity. In conclusion, our data identified Dlk1/FA1 as a downstream target of TGF-beta1 signaling molecule that mediates its function in embryonic chondrogenesis. The crosstalk between TGF-beta1 and Dlk1/FA1 was shown to promote early chondrogenesis during the embryonic endochondral ossification process.
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