Inhibition of transforming growth factor-beta/SMAD signalling by the interferon-gamma/STAT pathway.
Transforming growth factor-beta (TGF-beta) and interferon-gamma (IFN-gamma) have opposite effects on diverse cellular functions, but the basis for this antagonism is not known. TGF-beta signals through a receptor serine kinase that phosphorylates and activates the transcription factors Smads 2 and 3, whereas the IFN-gamma receptor and its associated protein tyrosine kinase Jak1 mediate phosphorylation and activation of the transcription factor Stat1. Here we present a basis for the integration of TGF-beta and IFN-gamma signals. IFN-gamma inhibits the TGF beta-induced phosphorylation of Smad3 and its attendant events, namely, the association of Smad3 with Smad4, the accumulation of Smad3 in the nucleus, and the activation of TGFbeta-responsive genes. Acting through Jak1 and Stat1, IFN-gamma induces the expression of Smad7, an antagonistic SMAD, which prevents the interaction of Smad3 with the TGF-beta receptor. The results indicate a mechanism of transmodulation between the STAT and SMAD signal-transduction pathways.
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Related Subject Headings
- Transforming Growth Factor beta
- Trans-Activators
- Smad7 Protein
- Smad3 Protein
- Signal Transduction
- STAT1 Transcription Factor
- Receptors, Transforming Growth Factor beta
- Protein-Tyrosine Kinases
- Phosphorylation
- Molecular Sequence Data
Citation
Published In
DOI
EISSN
ISSN
Publication Date
Volume
Issue
Start / End Page
Related Subject Headings
- Transforming Growth Factor beta
- Trans-Activators
- Smad7 Protein
- Smad3 Protein
- Signal Transduction
- STAT1 Transcription Factor
- Receptors, Transforming Growth Factor beta
- Protein-Tyrosine Kinases
- Phosphorylation
- Molecular Sequence Data