Cutting edge: The orphan nuclear receptor Nr4a1 regulates CD8+ T cell expansion and effector function through direct repression of IRF4

Heba N. Nowyhed, Tridu R. Huynh, Graham D. Thomas, Amy Blatchley, Catherine C. Hedrick

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

The transcription factor IFN regulatory factor (IRF)4 was shown to play a crucial role in the protective CD8+ T cell response; however, regulation of IRF4 expression in CD8+ T cells remains unclear. In this article, we report a critical role for Nr4a1 in regulating the expansion, differentiation, and function of CD8+ T cells through direct transcriptional repression of Irf4. Without Nr4a1, the regulation of IRF4 is lost, driving an increase in Irf4 expression and, in turn, resulting in a faster rate of CD8 T cell proliferation and expansion. Nr4a1-deficient mice show increases in CD8 T cell effector responses with improved clearance of Listeria monocytogenes. Our data support a novel and critical role for Nr4a1 in the regulation of CD8+ T cell expansion and effector function through transcriptional repression of Irf4.

Original languageEnglish (US)
Pages (from-to)3515-3519
Number of pages5
JournalJournal of Immunology
Volume195
Issue number8
DOIs
StatePublished - Oct 15 2015
Externally publishedYes

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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