Nur77 serves as a molecular brake of the metabolic switch during T cell activation to restrict autoimmunity

Proc Natl Acad Sci U S A. 2018 Aug 21;115(34):E8017-E8026. doi: 10.1073/pnas.1721049115. Epub 2018 Aug 2.

Abstract

T cells critically depend on reprogramming of metabolic signatures to meet the bioenergetic demands during activation and clonal expansion. Here we identify the transcription factor Nur77 as a cell-intrinsic modulator of T cell activation. Nur77-deficient T cells are highly proliferative, and lack of Nur77 is associated with enhanced T cell activation and increased susceptibility for T cell-mediated inflammatory diseases, such as CNS autoimmunity, allergic contact dermatitis and collagen-induced arthritis. Importantly, Nur77 serves as key regulator of energy metabolism in T cells, restricting mitochondrial respiration and glycolysis and controlling switching between different energy pathways. Transcriptional network analysis revealed that Nur77 modulates the expression of metabolic genes, most likely in close interaction with other transcription factors, especially estrogen-related receptor α. In summary, we identify Nur77 as a transcriptional regulator of T cell metabolism, which elevates the threshold for T cell activation and confers protection in different T cell-mediated inflammatory diseases.

Keywords: Nur77; T cells; autoimmunity; immunometabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmunity*
  • Central Nervous System / immunology
  • Central Nervous System / metabolism
  • ERRalpha Estrogen-Related Receptor
  • Gene Expression Profiling
  • Inflammation / genetics
  • Inflammation / immunology
  • Inflammation / metabolism
  • Lymphocyte Activation*
  • Mice
  • Mice, Knockout
  • Mitochondria* / genetics
  • Mitochondria* / immunology
  • Mitochondria* / metabolism
  • Nuclear Receptor Subfamily 4, Group A, Member 1* / genetics
  • Nuclear Receptor Subfamily 4, Group A, Member 1* / immunology
  • Nuclear Receptor Subfamily 4, Group A, Member 1* / metabolism
  • Oxygen Consumption / immunology*
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / immunology
  • Receptors, Estrogen / metabolism
  • T-Lymphocytes* / immunology
  • T-Lymphocytes* / metabolism

Substances

  • Nr4a1 protein, mouse
  • Nuclear Receptor Subfamily 4, Group A, Member 1
  • Receptors, Estrogen