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Cutting Edge: Changes in Histone Acetylation at the <i>IL-4</i> and <i>IFN-γ</i> Loci Accompany Th1/Th2 Differentiation
333
Citations
29
References
2002
Year
Lymphocyte DevelopmentEpigenetic ChangeImmunologyMolecular BiologyHistone Acetylation StatusCd4 T Cell ResponsesEpigeneticsTranscriptional RegulationChromatin ChangesCell SignalingGene ExpressionEpigenetic RegulationCell BiologySignature Cytokine LociChromatin FunctionChromatinChromatin StructureChromatin RemodelingNatural SciencesEpigenomicsCellular Immune ResponseTranscription FactorsMedicineHistone Acetylation
Peripheral T cell differentiation is accompanied by chromatin changes at the signature cytokine loci. Using chromatin immunoprecipitation we demonstrate that profound increases in histone acetylation occur at the IFN-gamma and IL-4 loci during Th1/Th2 differentiation. These changes in histone acetylation status are locus and lineage specific, and are maintained by the transcription factors Tbet and GATA3 in a STAT-dependent manner. Our results suggest a model of cytokine locus activation in which TCR signals initiate chromatin remodeling and locus opening in a cytokine-independent fashion. Subsequently, cytokine signaling reinforces polarization by expanding and maintaining the accessible state at the relevant cytokine locus (IL-4 or IFN-gamma). In this model, GATA3 and Tbet serve as transcriptional maintenance factors, which keep the locus accessible to the transcriptional machinery.
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