High-fat diet causes rapid loss of intestinal group 3 innate lymphoid cells through microbiota-driven inflammation and mitochondrial stress

 Highlights

  • •
    Microbiota-driven inflammation and lipid uptake drive intestinal ILC3 lipotoxicity
  • •
    Inflammatory signaling suppresses fatty acid oxidation in ILC3s but not Th17 cells
  • •
    ILC3-specific immunometabolic vulnerability is conserved in intestine of mice and human
  • •
    HFD-mediated intestinal ILC3 depletion is reversible upon dietary normalization

Summary

Group 3 innate lymphoid cells (ILC3s) are key sensors of the intestinal environment, integrating dietary and microbial cues to maintain intestinal immunity. We found that intestinal ILC3s were reduced in overweight and obese humans and in high-fat diet (HFD)-fed mice. ILC3 loss occurred independently of caloric excess, weight gain, or glucose intolerance. Instead, impairment arose within hours of HFD consumption and was initiated by microbiota-driven intestinal barrier permeability and concomitant activation of inflammatory mononuclear phagocytes (MNPs). This response to inflammation impaired fatty acid oxidation in lipid-loaded ILC3s, resulting in mitochondrial damage and cell death. Intestinal ILC3 cell death was rescued by removal of excess fats from the diet. ILC3s from individuals with obesity also exhibited impaired fatty acid oxidation. Together, our findings define a malleable mechanism whereby dietary fats and microbial cues drive ILC3 maladaptation and death, with consequences for intestinal homeostasis.

Read full article at:
https://www.sciencedirect.com/science/article/abs/pii/S1074761326000841



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