STAT6 is activated by growth factors and cytokines, especially by interleukin-4 and interleukin-13.
STAT6 shares structural similarity with the other STAT proteins and consists of the N-terminal domain, DNA binding domain, SH3-like domain, SH2 domain, and transactivation domain (TAD).[7]
STAT proteins are activated by Janus family tyrosine kinases (JAKs) in response to cytokine exposure. STAT6 is activated by the cytokines interleukin-4 (IL-4) and interleukin-13 (IL-13) with their receptors, both containing the α-subunit of the IL-4 receptor (IL-4Rα). Tyrosine phosphorylation of STAT6 after stimulation by IL-4 leads to the formation of STAT6 homodimers that bind specific DNA elements via a DNA-binding domain.
Function: The STAT6-mediated signaling pathway is required for T helper type 2 (Th2) cell development and the Th2 immune response. The STAT6 protein is critical for IL4-mediated biological responses.
Activation of the STAT6 pathway is important for macrophage function and is required for activation of the M2 subtype of macrophages.
The STAT6 protein also regulates other transcription factors such as Gata3, which is an important regulator of Th2 differentiation. STAT6 is also required for the development of interleukin-9-secreting T cells.
STAT6 also plays a critical role in Th2 inflammatory responses in the lung, including clearance of parasitic infections and in the pathogenesis of asthma.
STAT6 interacts with:
-
CREB-binding protein
- EP300
- IRF4
- NFKB1
- Nuclear receptor coactivator 1
- SND1.