Journal of Biological Chemistry · 2014 · 25 citations · 32 references
Life SciencesCell BiologyImmunologyCellular ImmunologySignal TransductionTranscriptional RegulationCell-mediated ImmunityCytokine BiologyHelper T Cell SubsetsImmune Cell SignalingT Cell ActivationT Cell BiologyCytokine-mediated T Cell ResponsesT Cell Activation CytokinesT Helper 2 DifferentiationT Helper 2 Immune ResponsesTh2 Effector FunctionTh2 Immune Response
Th2 memory lymphocytes have imprinted their Il4 genes epigenetically for expression in dependence of T cell receptor restimulation. However, in a given restimulation, not all Th cells with a memory for IL-4 expression express IL-4. Here, we show that in reactivated Th2 cells, the transcription factors NFATc2, NF-kB p65, c-Maf, p300, Brg1, STAT6, and GATA-3 assemble at the Il4 promoter in Th2 cells expressing IL-4 but not in Th2 cells not expressing it. NFATc2 is critical for assembly of this transcription factor complex. Because NFATc2 translocation into the nucleus occurs in an all-or-none fashion, dependent on complete dephosphorylation by calcineurin, NFATc2 controls the frequencies of cells reexpressing Il4, translates analog differences in T cell receptor stimulation into a digital decision for Il4 reexpression, and instructs all reexpressing cells to express the same amount of IL-4. This analog-to-digital conversion may be critical for the immune system to respond to low concentrations of antigens.
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