| Literature DB >> 33730567 |
Jasmine Li1, Kristine Hardy2, Moshe Olshansky1, Adele Barugahare1, Linden J Gearing3, Julia E Prier4, Xavier Y X Sng5, Michelle Ly Thai Nguyen4, Dana Piovesan4, Brendan E Russ1, Nicole L La Gruta5, Paul J Hertzog3, Sudha Rao6, Stephen J Turner7.
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.Entities:
Keywords: CD8(+) T cell; T cell activation; T cell memory; chromatin; histone demethylase; virus immunity
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Year: 2021 PMID: 33730567 DOI: 10.1016/j.celrep.2021.108839
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423