The pathogen recognition receptor NOD2 regulates human FOXP3+ T cell survival

J Immunol. 2010 Jun 15;184(12):7247-56. doi: 10.4049/jimmunol.0901479. Epub 2010 May 7.

Abstract

The expression of pathogen recognition receptors in human FOXP3+ T regulatory cells is established, yet the function of these receptors is currently obscure. In the process of studying the function of both peripheral and lamina propria FOXP3+ lymphocytes in patients with the human inflammatory bowel disease Crohn's disease, we observed a clear deficiency in the quantity of FOXP3+ lymphocytes in patients with disease-associated polymorphisms in the pathogen recognition receptor gene NOD2. Subsequently, we determined that the NOD2 ligand, muramyl dipeptide (MDP), activates NF-kappaB in primary human FOXP3+ T cells. This activation is functionally relevant, as MDP-stimulated human FOXP3+ T cells are protected from death receptor Fas-mediated apoptosis. Importantly, apoptosis protection was not evident in MDP-stimulated FOXP3+ T cells isolated from a patient with the disease-associated polymorphism. Thus, we propose that one function of pathogen recognition receptors in human T regulatory cells is the protection against death receptor-mediated apoptosis in a Fas ligand-rich environment, such as that of the inflamed intestinal subepithelial space.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / genetics
  • Apoptosis / immunology*
  • Blotting, Western
  • Cell Separation
  • Cell Survival
  • Crohn Disease / genetics
  • Crohn Disease / immunology*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Flow Cytometry
  • Forkhead Transcription Factors / immunology*
  • Forkhead Transcription Factors / metabolism
  • Genotype
  • Humans
  • Immunohistochemistry
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism
  • Male
  • Middle Aged
  • Nod2 Signaling Adaptor Protein / genetics
  • Nod2 Signaling Adaptor Protein / immunology*
  • Nod2 Signaling Adaptor Protein / metabolism
  • Polymorphism, Single Nucleotide
  • RNA, Small Interfering
  • Reverse Transcriptase Polymerase Chain Reaction
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • Transfection

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein
  • RNA, Small Interfering