IL-4/STAT6 immune axis regulates peripheral nutrient metabolism and insulin sensitivity

Proc Natl Acad Sci U S A. 2010 Dec 28;107(52):22617-22. doi: 10.1073/pnas.1009152108. Epub 2010 Dec 13.

Abstract

Immune cells take residence in metabolic tissues, providing a framework for direct regulation of nutrient metabolism. Despite conservation of this anatomic relationship through evolution, the signals and mechanisms by which the immune system regulates nutrient homeostasis and insulin action remain poorly understood. Here, we demonstrate that the IL-4/STAT6 immune axis, a key pathway in helminth immunity and allergies, controls peripheral nutrient metabolism and insulin sensitivity. Disruption of signal transducer and activator of transcription 6 (STAT6) decreases insulin action and enhances a peroxisome proliferator-activated receptor α (PPARα) driven program of oxidative metabolism. Conversely, activation of STAT6 by IL-4 improves insulin action by inhibiting the PPARα-regulated program of nutrient catabolism and attenuating adipose tissue inflammation. These findings have thus identified an unexpected molecular link between the immune system and macronutrient metabolism, suggesting perhaps the coevolution of these pathways occurred to ensure access to glucose during times of helminth infection.

Publication types

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

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism
  • Animals
  • Cell Line
  • Cells, Cultured
  • Dietary Fats / administration & dosage
  • Dietary Fats / adverse effects
  • Energy Metabolism / drug effects*
  • Female
  • Hepatocytes / cytology
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Immunoblotting
  • Insulin Resistance / physiology*
  • Interleukin-4 / pharmacology*
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Obesity / etiology
  • Obesity / metabolism
  • Obesity / physiopathology
  • PPAR alpha / metabolism
  • Phosphorylation / drug effects
  • STAT6 Transcription Factor / genetics
  • STAT6 Transcription Factor / metabolism*
  • Signal Transduction / drug effects

Substances

  • Dietary Fats
  • PPAR alpha
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Interleukin-4