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Cell Rep ; 34(11): 108839, 2021 03 16.
Article in English | MEDLINE | ID: mdl-33730567

ABSTRACT

Naive CD8+ T cell activation results in an autonomous program of cellular proliferation and differentiation. However, the mechanisms that underpin this process are unclear. Here, we profile genome-wide changes in chromatin accessibility, gene transcription, and the deposition of a key chromatin modification (H3K27me3) early after naive CD8+ T cell activation. Rapid upregulation of the histone demethylase KDM6B prior to the first cell division is required for initiating H3K27me3 removal at genes essential for subsequent T cell differentiation and proliferation. Inhibition of KDM6B-dependent H3K27me3 demethylation limits the magnitude of an effective primary virus-specific CD8+ T cell response and the formation of memory CD8+ T cell populations. Accordingly, we define the early spatiotemporal events underpinning early lineage-specific chromatin reprogramming that are necessary for autonomous CD8+ T cell proliferation and differentiation.


Subject(s)
CD8-Positive T-Lymphocytes/immunology , Cell Differentiation/immunology , Chromatin Assembly and Disassembly , Jumonji Domain-Containing Histone Demethylases/metabolism , Viruses/immunology , Animals , Demethylation , Female , Histones/metabolism , Humans , Immunologic Memory , Lymphocyte Activation , Lysine/metabolism , Male , Mice, Inbred C57BL , Protein Binding , Transcription Factors/metabolism , Up-Regulation
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