Accumulation of microbial DNAs promotes to islet inflammation and β cell abnormalities in obesity in mice

Nat Commun. 2022 Jan 28;13(1):565. doi: 10.1038/s41467-022-28239-2.

Abstract

Various microbial products leaked from gut lumen exacerbate tissue inflammation and metabolic disorders in obesity. Vsig4+ macrophages are key players preventing infiltration of bacteria and their products into host tissues. However, roles of islet Vsig4+ macrophages in the communication between microbiota and β cells in pathogenesis of obesity-associated islet abnormalities are unknown. Here, we find that bacterial DNAs are enriched in β cells of individuals with obesity. Intestinal microbial DNA-containing extracellular vesicles (mEVs) readily pass through obese gut barrier and deliver microbial DNAs into β cells, resulting in elevated inflammation and impaired insulin secretion by triggering cGAS/STING activation. Vsig4+ macrophages prevent mEV infiltration into β cells through a C3-dependent opsonization, whereas loss of Vsig4 leads to microbial DNA enrichment in β cells after mEV treatment. Removal of microbial DNAs blunts mEV effects. Loss of Vsig4+ macrophages leads to microbial DNA accumulation in β cells and subsequently obesity-associated islet abnormalities.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • DNA, Bacterial / blood
  • DNA, Bacterial / genetics
  • DNA, Bacterial / metabolism*
  • Diet, High-Fat / adverse effects
  • Extracellular Vesicles / genetics
  • Extracellular Vesicles / metabolism
  • Gastrointestinal Microbiome / genetics
  • Humans
  • Inflammation / etiology
  • Inflammation / genetics
  • Inflammation / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / metabolism*
  • Islets of Langerhans / metabolism*
  • Islets of Langerhans / pathology
  • Macrophages / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / metabolism
  • Obesity / genetics
  • Obesity / metabolism*
  • Receptors, Complement / genetics
  • Receptors, Complement / metabolism
  • Signal Transduction / genetics

Substances

  • DNA, Bacterial
  • Membrane Proteins
  • Receptors, Complement
  • Sting1 protein, mouse
  • VSIG4 protein, mouse
  • Nucleotidyltransferases
  • cGAS protein, mouse