Journal article
Hyperactivation of Stat3 in gp130 mutant mice promotes gastric hyperproliferation and desensitizes TGF-β signaling
BJ Jenkins, D Grail, T Nheu, M Najdovska, B Wang, P Waring, M Inglese, RM McLoughlin, SA Jones, N Topley, H Baumann, LM Judd, AS Giraud, A Boussioutas, HJ Zhu, M Ernst
Nature Medicine | NATURE PUBLISHING GROUP | Published : 2005
DOI: 10.1038/nm1282
Abstract
The latent transcription factor Stat3 is activated by gp130, the common receptor for the interleukin (IL)-6 cytokine family and other growth factor and cytokine receptors. Ligand-induced dimerization of gp130 leads to activation of the Stat1, Stat3 and Shp2-Ras-Erk signaling pathways. Here we assess genetically the contribution of exaggerated Stat3 activation to the phenotype of gp130 Y757F/Y757F mice, in which a knock-in mutation disrupts the negative feedback mechanism on gp130-dependent Stat signaling. Compared to gp130 Y757F/Y757F mice, reduced Stat3 activation in gp130 Y757F/Y757F Stat3+/- mice increased their lifespan, prevented splenomegaly, normalized exaggerated hepatic acute-phase ..
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