Nucleotide-binding oligomerization domain-containing protein 2 (Nod2) modulates T1DM susceptibility by gut microbiota

J Autoimmun. 2017 Aug:82:85-95. doi: 10.1016/j.jaut.2017.05.007. Epub 2017 Jun 4.

Abstract

Nucleotide-binding oligomerization domain-containing protein 2 (Nod2) is an innate immune receptor. To investigate the role of Nod2 in susceptibility to the autoimmune disease, type 1 diabetes mellitus (T1DM), we generated Nod2-/- non-obese diabetic (NOD) mice. The Nod2-/-NOD mice had different composition of the gut microbiota compared to Nod2+/+NOD mice and were significantly protected from diabetes, but only when housed separately from Nod2+/+NOD mice. This suggested that T1DM susceptibility in Nod2-/-NOD mice is dependent on the alteration of gut microbiota, which modulated the frequency and function of IgA-secreting B-cells and IL-10 promoting T-regulatory cells. Finally, colonizing germ-free NOD mice with Nod2-/-NOD gut microbiota significantly reduced pro-inflammatory cytokine-secreting immune cells but increased T-regulatory cells. Thus, gut microbiota modulate the immune system and T1D susceptibility. Importantly, our study raises a critical question about the housing mode in the interpretation of the disease phenotype of genetically-modified mouse strains in T1DM studies.

Keywords: Gut microbiota; Innate immunity; NOD; Nod2; Type 1 diabetes mellitus.

MeSH terms

  • Animals
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • Cytokines / metabolism
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Diabetes Mellitus, Type 1 / etiology*
  • Disease Models, Animal
  • Disease Susceptibility*
  • Female
  • Gastrointestinal Microbiome* / immunology
  • Humans
  • Immunity, Innate
  • Immunoglobulin A, Secretory / immunology
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mice, Inbred NOD
  • Mice, Knockout
  • Nod2 Signaling Adaptor Protein / genetics*
  • Nod2 Signaling Adaptor Protein / metabolism
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Cytokines
  • Immunoglobulin A, Secretory
  • Nod2 Signaling Adaptor Protein
  • Nod2 protein, mouse