Egr2 induced during DC development acts as an intrinsic negative regulator of DC immunogenicity

Eur J Immunol. 2013 Sep;43(9):2484-96. doi: 10.1002/eji.201243046. Epub 2013 Jul 1.

Abstract

Early growth response gene 2 (Egr2), which encodes a zinc finger transcription factor, is rapidly and transiently induced in various cell types independently of de novo protein synthesis. Although a role for Egr2 is well established in T-cell development, Egr2 expression and its biological function in dendritic cells (DCs) have not yet been described. Here, we demonstrate Egr2 expression during DC development, and its role in DC-mediated immune responses. Egr2 is expressed in the later stage of DC development from BM precursor cells. Even at steady state, Egr2 is highly expressed in mouse splenic DCs. Egr2-knockdown (Egr2-KD) DCs showed increased levels of major histocompatability complex (MHC) class I and II and co-stimulatory molecules, and enhanced antigen uptake and migratory capacities. Furthermore, Egr2-KD abolished SOCS1 expression and signal transducer and activator of transcription 5 (STAT5) activation during DC development, probably resulting in the enhancement of IL-12 expression and Th1 immunogenicity of a DC vaccine. DC-mediated cytotoxic T lymphocyte (CTL) activation and antitumor immunity were significantly enhanced by Egr2-KD, and impaired by Egr2 overexpression in antigen-pulsed DC vaccines. These data suggest that Egr2 acts as an intrinsic negative regulator of DC immunogenicity and can be an attractive molecular target for DC vaccine development.

Keywords: DC development; Egr2; Immunotherapy; Negative regulator; Th1 immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / immunology
  • Bone Marrow Cells / metabolism
  • Cancer Vaccines / immunology
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Early Growth Response Protein 2 / genetics*
  • Early Growth Response Protein 2 / metabolism*
  • Female
  • Genes, MHC Class I
  • Genes, MHC Class II
  • Interleukin-12 / biosynthesis
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • RNA Interference
  • RNA, Small Interfering
  • STAT5 Transcription Factor / metabolism
  • Spleen / cytology
  • Spleen / immunology
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling Proteins / biosynthesis
  • T-Lymphocytes, Cytotoxic / immunology
  • Th1 Cells / immunology

Substances

  • Cancer Vaccines
  • Early Growth Response Protein 2
  • Egr2 protein, mouse
  • RNA, Small Interfering
  • STAT5 Transcription Factor
  • Socs1 protein, mouse
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Interleukin-12