KDM6B-dependent chromatin remodeling underpins effective virus-specific CD8+ T cell differentiation

Cell Rep. 2021 Mar 16;34(11):108839. doi: 10.1016/j.celrep.2021.108839.

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.

Keywords: CD8(+) T cell; T cell activation; T cell memory; chromatin; histone demethylase; virus immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

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

Substances

  • Histones
  • Transcription Factors
  • Jumonji Domain-Containing Histone Demethylases
  • Kdm6b protein, mouse
  • Lysine