Interferon-sensitive response element (ISRE) is mainly responsible for IFN-alpha-induced upregulation of programmed death-1 (PD-1) in macrophages

Biochim Biophys Acta. 2008 Dec;1779(12):811-9. doi: 10.1016/j.bbagrm.2008.08.003. Epub 2008 Aug 15.

Abstract

Programmed death-1 (PD-1), an immunoinhibitory receptor, is upregulated in T cells, B cells, NKT cells, and monocytes upon activation. More specifically, T-cell-associated PD-1 is critically important for maintaining peripheral tolerance through the PD-1-B7-H1 pathway. However, the physiological role of macrophage-associated PD-1 remains unclear. We addressed the molecular mechanism underlying the regulation of PD-1 expression on macrophages in response to IFN-alpha. Based on a luciferase assay using promoter constructs, we found that the promoter region located between -1090 and -1105 nucleotides from the translational start site is essential for PD-1 expression. Electrophoretic mobility-shift assay and site-directed mutagenesis revealed that interferon-sensitive responsive element (ISRE) and STAT1 and STAT2 are primarily responsible for the constitutive expression of PD-1, as well as for the IFN-alpha-mediated upregulation of PD-1. In addition, AG490, a Janus-activated kinase/signal transducer and activator of transcription (JAK/STAT) inhibitor, markedly abolished the responsiveness of bone marrow-derived macrophages (BMM) to IFN-alpha. Our findings support the essential roles of ISRE, STAT1, and STAT2 in the regulation of constitutive and IFN-alpha-mediated PD-1 expression in macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism*
  • Apoptosis Regulatory Proteins / metabolism*
  • Base Sequence
  • Bone Marrow Cells / metabolism
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation*
  • Humans
  • Interferon-alpha / metabolism*
  • Macrophages / metabolism*
  • Mice
  • Molecular Sequence Data
  • Programmed Cell Death 1 Receptor
  • Response Elements*
  • STAT1 Transcription Factor / metabolism
  • STAT2 Transcription Factor / metabolism
  • Tyrphostins / pharmacology
  • Up-Regulation*

Substances

  • Antigens, CD
  • Apoptosis Regulatory Proteins
  • Enzyme Inhibitors
  • Interferon-alpha
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT2 Transcription Factor
  • STAT2 protein, human
  • Stat1 protein, mouse
  • Stat2 protein, mouse
  • Tyrphostins
  • alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide