Publication | Open Access
Lck Mediates Th2 Differentiation through Effects on T-bet and GATA-3
30
Citations
37
References
2010
Year
Th2 DifferentiationLymphocyte DevelopmentMolecular RegulationT-regulatory CellImmunologyImmune RegulationMolecular BiologyImmunologic MechanismCellular PhysiologyInflammationSignaling PathwayCell RegulationCell SignalingTh2 CellsAutoimmune DiseaseAutoimmunityGene ExpressionCell BiologyProtein PhosphorylationCytokineSignal TransductionDevelopmental BiologyImmune Cell DevelopmentTh2 Effector FunctionsNatural SciencesMedicine
The Src family kinase Lck has been shown to be crucial in T cell signaling and development. However, its role in Th effector functions is not well understood. Lck has previously been shown to play a role in the cytokine expression of Th2 cells, but the mechanism by which Lck influences Th2 effector functions is unknown. Using a mouse model, we report that Lck is important in regulating the expression of IL-4 in Th2 skewed cells but is not as necessary for the expression of Th2 cytokines IL-5, IL-10, and IL-13. Furthermore, in the absence of Lck, T-bet and GATA-3 expression is aberrant. Moreover, this atypical expression pattern of T-bet and GATA-3 correlates with increased histone 3 acetylation at the Ifng locus and production of the Th1 cytokine IFN-gamma. We find overexpression of GATA-3 restores IL-4 expression in lck(-/-) Th2 cells; this indicates that the decreased IL-4 expression is due in part to reduced amounts of GATA-3. Taken together, these data imply that Lck mediates Th2 differentiation through effects on T-bet and GATA-3.
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