Essential role of Stat6 in IL-4 signalling

Abstract

INTERLEUKIN-4(IL-4) is a pleiotropic lymphokine which plays an important role in the immune system¹. IL-4 activates two distinct signalling pathways through tyrosine phosphorylation of Stat6, a signal transducer and activator of transcription, and of a 170K protein called 4PS^2–7. To investigate the functional role of Stat6 in IL-4 signalling, we generated mice deficient in Stat6 by gene targeting. We report here that in the mutant mice, expression of CD23 and major histocompatibility complex (MHC) class II in resting B cells was not enhanced in response to IL-4. IL-4-induced B-cell proliferation costimulated by anti-IgM antibody was abolished. The T-cell proliferative response was also notably reduced. Furthermore, production of Th2 cytokines from T cells as well as IgE and IgGl responses after nematode infection were profoundly reduced. These findings agreed with those obtained in IL-4-deficient mice^8,9 or using antibodies to IL-4¹⁰ and the IL-4 receptor¹¹. We conclude that Stat6 plays a central role in exerting IL-4-mediated biological responses.