Direct and indirect induction by 1,25-dihydroxyvitamin D3 of the NOD2/CARD15-defensin beta2 innate immune pathway defective in Crohn disease

J Biol Chem. 2010 Jan 22;285(4):2227-31. doi: 10.1074/jbc.C109.071225. Epub 2009 Nov 30.

Abstract

Vitamin D signaling through its nuclear vitamin D receptor has emerged as a key regulator of innate immunity in humans. Here we show that hormonal vitamin D, 1,25-dihydroxyvitamin D(3), robustly stimulates expression of pattern recognition receptor NOD2/CARD15/IBD1 gene and protein in primary human monocytic and epithelial cells. The vitamin D receptor signals through distal enhancers in the NOD2 gene, whose function was validated by chromatin immunoprecipitation and chromatin conformation capture assays. A key downstream signaling consequence of NOD2 activation by agonist muramyl dipeptide is stimulation of NF-kappaB transcription factor function, which induces expression of the gene encoding antimicrobial peptide defensin beta2 (DEFB2/HBD2). Pretreatment with 1,25-dihydroxyvitamin D(3) synergistically induced NF-kappaB function and expression of genes encoding DEFB2/HBD2 and antimicrobial peptide cathelicidin in the presence of muramyl dipeptide. Importantly, this synergistic response was also seen in macrophages from a donor wild type for NOD2 but was absent in macrophages from patients with Crohn disease homozygous for non-functional NOD2 variants. These studies provide strong molecular links between vitamin D deficiency and the genetics of Crohn disease, a chronic incurable inflammatory bowel condition, as Crohn's pathogenesis is associated with attenuated NOD2 or DEFB2/HBD2 function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylmuramyl-Alanyl-Isoglutamine / pharmacology
  • Adjuvants, Immunologic / pharmacology
  • Calcitriol / metabolism
  • Calcitriol / pharmacology*
  • Crohn Disease* / genetics
  • Crohn Disease* / immunology
  • Crohn Disease* / metabolism
  • Drug Synergism
  • Epithelial Cells / immunology
  • Humans
  • Macrophages / immunology
  • Macrophages / metabolism
  • Monocytes / immunology
  • Monocytes / metabolism
  • NF-kappa B / metabolism
  • Nod2 Signaling Adaptor Protein / genetics*
  • Signal Transduction / immunology
  • Transcriptional Activation / immunology
  • Vitamin D Deficiency* / genetics
  • Vitamin D Deficiency* / immunology
  • Vitamin D Deficiency* / metabolism
  • beta-Defensins / genetics*

Substances

  • Adjuvants, Immunologic
  • DEFB4A protein, human
  • NF-kappa B
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein
  • beta-Defensins
  • Acetylmuramyl-Alanyl-Isoglutamine
  • Calcitriol