Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity

Hong Yu, Hiroshi Nishio, Joseph Barbi, Marisa Mitchell-Flack, Paolo D.A. Vignali, Ying Zheng, Andriana Lebid, Kwang Yu Chang, Juan Fu, Makenzie Higgins, Ching Tai Huang, Xuehong Zhang, Zhiguang Li, Lee Blosser, Ada Tam, Charles Drake, Drew Pardoll

Research output: Contribution to journalArticlepeer-review

Abstract

The adaptive T cell response is accompanied by continuous rewiring of the T cell's electric and metabolic state. Ion channels and nutrient transporters integrate bioelectric and biochemical signals from the environment, setting cellular electric and metabolic states. Divergent electric and metabolic states contribute to T cell immunity or tolerance. Here, we report in mice that neuritin (Nrn1) contributes to tolerance development by modulating regulatory and effector T cell function. Nrn1 expression in regulatory T cells promotes its expansion and suppression function, while expression in the T effector cell dampens its inflammatory response. Nrn1 deficiency in mice causes dysregulation of ion channel and nutrient transporter expression in Treg and effector T cells, resulting in divergent metabolic outcomes and impacting autoimmune disease progression and recovery. These findings identify a novel immune function of the neurotrophic factor Nrn1 in regulating the T cell metabolic state in a cell context-dependent manner and modulating the outcome of an immune response.

Original languageEnglish (US)
JournaleLife
Volume13
DOIs
StatePublished - Nov 20 2024

Keywords

  • Treg
  • autoimmunity
  • cell fate
  • effector T cell
  • electric state
  • immunology
  • inflammation
  • metabolism
  • mouse

ASJC Scopus subject areas

  • General Neuroscience
  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology

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