IMR Press / FBL / Volume 10 / Issue 1 / DOI: 10.2741/1563

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with Frontiers in Bioscience.


TGF-β signaling in chondrocytes

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1 Center for Musculoskeletal Research, Department of Orthopaedics, University of Rochester School of Medicine, Rochester, NY 14642, USA
Front. Biosci. (Landmark Ed) 2005, 10(1), 681–688;
Published: 1 January 2005

Transforming growth factor-β (TGF-β) regulates a large variety of cellular activities. Binding of TGF-β to its cell surface receptor triggers several signaling cascades, among which the TGF-β-Smad pathway is the most extensively studied. TGF-β also activates protein kinases, including MAPK, PKA and PKC, and modulates gene expression via its delicate interaction with other signaling pathways. During endochondral bone formation, TGF-β acts as a potent inhibitor of the terminal differentiation of epiphyseal growth plate chondrocytes. This effect appears to be primarily mediated by Smad molecules, although MAPK-ATF2 signaling is also involved. The rate of chondrocyte maturation is tightly regulated through the interactions of Smad-mediated signaling, the Wnt signaling pathway, and the transcription factor Runx2. Improving our understanding of the exact mechanisms underlying TGF-β-mediated signaling pathways and their effects may greatly impact the diagnosis and treatment of many common orthopaedic diseases.

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