Notch signaling regulates PD-1 expression during CD8(+) T-cell activation

Immunol Cell Biol. 2013 Jan;91(1):82-8. doi: 10.1038/icb.2012.53. Epub 2012 Oct 16.

Abstract

Programmed cell death 1 (PD-1) is an inhibitory receptor involved in T-cell activation, tolerance and exhaustion. Little is known on how the expression of PD-1 is controlled during T-cell activation. Recent studies demonstrated that NFATc1 and IRF9 regulate Pdcd1 (PD-1) transcription and that T-bet acts as a transcriptional repressor. In this study, we have investigated the role of the Notch signaling pathway in PD-1 regulation. Using specific inhibitors of the Notch signaling pathway, we showed decreased PD-1 expression and inhibition of Pdcd1 transcription by activated CD8(+) T cells. Chromatin immunoprecipitation further showed occupancy of the Pdcd1 promoter with RBPJk and Notch1 intracellular domain at RBPJk-binding sites. Our results identify the Notch signaling pathway as an important regulator of PD-1 expression by activated CD8(+) T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Cell Line
  • Gene Expression Regulation / genetics
  • Gene Expression Regulation / immunology*
  • Interferon-Stimulated Gene Factor 3, gamma Subunit / genetics
  • Interferon-Stimulated Gene Factor 3, gamma Subunit / immunology
  • Interferon-Stimulated Gene Factor 3, gamma Subunit / metabolism
  • Lymphocyte Activation / physiology*
  • Mice
  • NFATC Transcription Factors / genetics
  • NFATC Transcription Factors / immunology
  • NFATC Transcription Factors / metabolism
  • Programmed Cell Death 1 Receptor / biosynthesis
  • Programmed Cell Death 1 Receptor / genetics
  • Programmed Cell Death 1 Receptor / immunology*
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / immunology*
  • Receptor, Notch1 / metabolism
  • Response Elements / genetics
  • Response Elements / immunology
  • Signal Transduction / physiology*
  • Transcription, Genetic / genetics
  • Transcription, Genetic / immunology

Substances

  • IRF9 protein, mouse
  • Interferon-Stimulated Gene Factor 3, gamma Subunit
  • NFATC Transcription Factors
  • Nfatc1 protein, mouse
  • Notch1 protein, mouse
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor
  • Receptor, Notch1