TMED4 facilitates regulatory T cell suppressive function via ROS homeostasis in tumor and autoimmune mouse models

J Clin Invest. 2024 Oct 31;135(1):e179874. doi: 10.1172/JCI179874.

Abstract

Endoplasmic reticulum stress (ERS) plays crucial roles in maintaining Treg stability and function, yet the underlying mechanism remains largely unexplored. Here, we demonstrate that (Tmed4ΔTreg) mice with Treg-specific KO of ERS-related protein transmembrane p24 trafficking protein 4 (TMED4) had more Tregs with impaired Foxp3 stability, Treg signatures, and suppressive activity, which led to T cell hyperactivation and an exacerbated inflammatory phenotype and boosted antitumor immunity in mice. Mechanistically, loss of Tmed4 caused defects in ERS and a nuclear factor erythroid 2-related factor 2-related (NRF2-related) antioxidant response, which resulted in excessive ROS that reduced the Foxp3 stability and suppressive function of Tregs in an IRE1α/XBP1 axis-dependent manner. The abnormalities could be effectively rescued by the ROS scavenger, NRF2 inducer, or by forcible expression of IRE1α. Moreover, TMED4 suppressed IRE1α proteosome degradation via the ER-associated degradation (ERAD) system including the ER chaperone binding immunoglobulin protein (BIP). Our study reveals that TMED4 maintained the stability of Tregs and their suppressive function through IRE1α-dependent ROS and the NRF2-related antioxidant response.

Keywords: Adaptive immunity; Autoimmune diseases; Immunology; T cells.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Endoplasmic Reticulum Stress* / immunology
  • Endoribonucleases / genetics
  • Endoribonucleases / immunology
  • Endoribonucleases / metabolism
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / immunology
  • Forkhead Transcription Factors / metabolism
  • Homeostasis* / immunology
  • Membrane Proteins / genetics
  • Membrane Proteins / immunology
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Knockout*
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / immunology
  • NF-E2-Related Factor 2 / metabolism
  • Protein Serine-Threonine Kinases* / genetics
  • Protein Serine-Threonine Kinases* / immunology
  • Protein Serine-Threonine Kinases* / metabolism
  • Reactive Oxygen Species* / metabolism
  • T-Lymphocytes, Regulatory* / immunology
  • X-Box Binding Protein 1

Substances

  • Reactive Oxygen Species
  • Protein Serine-Threonine Kinases
  • NF-E2-Related Factor 2
  • Endoribonucleases
  • Membrane Proteins
  • Ern1 protein, mouse
  • Foxp3 protein, mouse
  • Nfe2l2 protein, mouse
  • Forkhead Transcription Factors
  • Xbp1 protein, mouse
  • X-Box Binding Protein 1