Human immature myeloid dendritic cells trigger a TH2-polarizing program via Jagged-1/Notch interaction

J Allergy Clin Immunol. 2008 Apr;121(4):1000-5.e8. doi: 10.1016/j.jaci.2008.01.004. Epub 2008 Mar 4.

Abstract

Background: The mechanisms by which human dendritic cells (DCs) activate a TH1-polarizing or TH2-polarizing program are still partially unclear.

Objective: Study of the mechanisms responsible for the TH1/TH2-polarizing activity of human circulating myeloid DCs before and after ligation of their Toll-like receptors (TLRs).

Methods: IL-4 and IFN-gamma production by CD4+ T cells was assessed in cocultures with myeloid DCs before or after TLR triggering. Expression of Jagged-1 and Delta-4 Notch ligands and of GATA-3 and T-box expressed in T cells transcription factors was evaluated by real-time quantitative PCR. Signal transducer and activator of transcription 4 and 6 phosphorylation was assessed by flow cytometry. Knockdown of Jagged-1 or Delta-4 was performed by transfection of DCs with appropriate silencing mRNAs.

Results: Myeloid immature DCs constitutively expressed Jagged-1, which induces in CD4+ T cells a TH2 polarization, as shown by Jagged-1 gene silencing. The TH2 polarization associated with high GATA-3/T-box expressed in T cells ratio and was at least partially dependent on the early induction of IL-4. Maturation of DCs by TLR ligation resulted in the reduction of Jagged-1 and upregulation of Delta-4, which was at least in part responsible for the polarization of CD4+ T cells to the TH1 phenotype.

Conclusion: CD4+ T-cell responses are usually characterized by a prevalent TH2 phenotype unless TLRs are triggered on DCs by microbial components.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • Calcium-Binding Proteins / metabolism*
  • Calcium-Binding Proteins / physiology
  • Cell Communication / immunology*
  • Cell Differentiation / immunology*
  • Cells, Cultured
  • Dendritic Cells / cytology
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • GATA3 Transcription Factor / biosynthesis
  • GATA3 Transcription Factor / genetics
  • Humans
  • Immunophenotyping
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Intercellular Signaling Peptides and Proteins / physiology
  • Jagged-1 Protein
  • Membrane Proteins / metabolism*
  • Membrane Proteins / physiology
  • Myeloid Progenitor Cells / cytology
  • Myeloid Progenitor Cells / immunology*
  • Myeloid Progenitor Cells / metabolism
  • Receptors, Notch / metabolism*
  • Receptors, Notch / physiology
  • Serrate-Jagged Proteins
  • T-Box Domain Proteins / biosynthesis
  • T-Box Domain Proteins / genetics
  • Th2 Cells / cytology
  • Th2 Cells / immunology*
  • Th2 Cells / metabolism*
  • Up-Regulation / genetics
  • Up-Regulation / immunology

Substances

  • Calcium-Binding Proteins
  • GATA3 Transcription Factor
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • Jagged-1 Protein
  • Membrane Proteins
  • Receptors, Notch
  • Serrate-Jagged Proteins
  • T-Box Domain Proteins
  • T-box transcription factor TBX21