IL-4 acts as a potent stimulator of IFN-? expression in CD8+ T cells through STAT6-dependent and independent induction of Eomesodermin and T-bet.

ABSTRACT: CD8+ T cell synthesis of IFN-? is an important component of the CD8+ T cell immune response. In short-term cultures of murine pan-T cells, we found that IL-4 was the principal cytokine responsible for driving IFN-? synthesis by CD3/CD28-activated CD8+ T cells. IL-4 was able to induce low levels of IFN-? mRNA in CD8+ T cells even in the absence of CD3/CD28 engagement, although concomitant CD3/CD28 stimulation was necessary for IFN-? secretion. IL-4 induction of IFN-? was explained by its ability to induce Eomesodermin and T-bet transcription factors whose expression was further increased by CD3/CD28. Expression of Eomesodermin, T-bet and IFN-? induced by IL-4 was partially dependent upon activation of MAPK and PI3K but independent of the canonical IL-4-activated transcription factor, STAT6. In contrast, expression of IFN-? induced by IL-4/CD3/CD28 stimulation showed additional dependency upon STAT6 which functions to increase expression of Eomesodermin specifically. These novel findings point to a function for IL-4 as a direct regulator of IFN-? expression in CD8+ T cells and reveal the molecular mechanisms involved.

SUBMITTER: Oliver JA 

PROVIDER: S-EPMC3246089 | biostudies-literature | 2012 Jan

REPOSITORIES: biostudies-literature