Metabolic disruption exacerbates intestinal damage during sleep deprivation by abolishing HIF1α-mediated repair

Cell Rep. 2024 Nov 26;43(11):114915. doi: 10.1016/j.celrep.2024.114915. Epub 2024 Nov 10.

Abstract

Sleep deprivation (SD) has been reported to induce intestinal damage by several mechanisms, yet its role in modulating epithelial repair remains unclear. In this study, we find that chronic SD leads to colonic damage through continuous hypoxia. However, HIF1α, which generally responds to hypoxia to modulate barrier integrity, was paradoxically dysregulated in the colon. Further investigation revealed that a metabolic disruption during SD causes accumulation of α-ketoglutarate in the colon. The excessive α-ketoglutarate degrades HIF1α protein through PHD2 (prolyl hydroxylase 2) to abolish the intestinal repair functions of HIF1α. Collectively, these findings provide insights into how SD can exacerbate intestinal damage by fine-tuning metabolism to abolish HIF1α-mediated repair.

Keywords: CP: Metabolism; CP: Neuroscience; HIF1α; PHD2; intestinal barrier repairing; metabolic dysfunction; sleep deprivation; α-ketoglutarate.

MeSH terms

  • Animals
  • Colon / metabolism
  • Colon / pathology
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit* / metabolism
  • Hypoxia-Inducible Factor-Proline Dioxygenases* / metabolism
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Intestines / pathology
  • Ketoglutaric Acids / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Sleep Deprivation* / metabolism
  • Sleep Deprivation* / pathology

Substances

  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • Ketoglutaric Acids
  • Egln1 protein, mouse
  • Hif1a protein, mouse