Differential regulation of Notch ligands in dendritic cells upon interaction with T helper cells

Scand J Immunol. 2011 Jul;74(1):62-70. doi: 10.1111/j.1365-3083.2011.02541.x.

Abstract

The Notch signalling pathway has recently been linked to T helper 1 (Th1)/T helper 2 (Th2) cell polarization via a mechanism involving differential expression of Notch ligands, Delta-like and Jagged, in antigen-presenting cells. However, whether stimuli other than pathogen-derived factors are involved in the regulation of Notch ligand expression in dendritic cells (DCs) remains unknown. Here, we address the effect of T helper cells (Th1 and Th2) on Delta-like 4 and Jagged 2 expression in bone marrow-derived DCs. We demonstrate that both Th1 and Th2 cells induce Delta-like 4 mRNA expression in DCs, in a process that is, in part, mediated by CD40 signalling. In contrast, only Th2 cells induce a significant increase in Jagged 2 mRNA levels in DCs. Additionally, we show that IL-4, a hallmark Th2 cytokine, plays a role in Jagged 2 expression, as evidenced by the fact that cholera toxin, a Th2-promoting stimulus, induces Jagged 2 mRNA expression in DCs only in the presence of IL-4. Finally, we demonstrate that DCs also express Notch 1 and that this expression is downregulated by IL-4. These data suggest that Notch ligands are differentially regulated in DCs: Delta-like 4 is regulated by T helper cells and by pathogen-derived Th1 stimuli, whereas Jagged 2 is regulated by Th2 cells and pathogen-derived Th2-promoting stimuli. Based on our results, we propose that the positive feedback loop that Th2 cells exert on T cell polarization may involve the induction of Jagged 2 expression in DCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • CD40 Antigens / immunology
  • Calcium-Binding Proteins
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Host-Pathogen Interactions / immunology
  • Interleukin-4 / immunology
  • Intracellular Signaling Peptides and Proteins / genetics
  • Jagged-2 Protein
  • Membrane Proteins / biosynthesis*
  • Membrane Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Signal Transduction
  • Th1 Cells / immunology*
  • Th2 Cells / immunology*

Substances

  • Adaptor Proteins, Signal Transducing
  • CD40 Antigens
  • Calcium-Binding Proteins
  • DLL4 protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • Jag2 protein, mouse
  • Jagged-2 Protein
  • Membrane Proteins
  • Interleukin-4