Sleep loss induces cholesterol-associated myelin dysfunction

Proc Natl Acad Sci U S A. 2026 Jan 27;123(4):e2523438123. doi: 10.1073/pnas.2523438123. Epub 2026 Jan 20.

Abstract

The increasing prevalence of sleep deprivation poses a public health challenge in modern society. Manifestations of reduced alertness, such as slowed reaction times and increased errors, are well-documented behavioral indicators of sleep loss (SL). Yet, the biological consequences of sleep deprivation and their role in behavioral impairment remain elusive. Our study reveals significant effects of sleep deprivation on myelin integrity. As a result, we identify increased conduction delays in nerve signal propagation, hindered interhemispheric synchronization, and impaired cognitive and motor performance associated with SL. By profiling oligodendrocyte transcriptome and lipidome, we observe SL-induced endoplasmic reticulum stress and lipid metabolism dysregulation, particularly affecting cholesterol homeostasis. Boosting cholesterol transport to myelin sheaths prevents SL effects on nerve signal propagation and behavior. Our findings highlight a possible role of oligodendrocyte cholesterol dysregulation in behavioral deficits associated with SL and unveil a novel target for intervention.

Keywords: myelin; oligodendrocyte; sleep; white matter.

MeSH terms

  • Animals
  • Cholesterol* / metabolism
  • Endoplasmic Reticulum Stress
  • Lipid Metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myelin Sheath* / metabolism
  • Myelin Sheath* / pathology
  • Oligodendroglia / metabolism
  • Oligodendroglia / pathology
  • Sleep Deprivation* / metabolism
  • Sleep Deprivation* / physiopathology

Substances

  • Cholesterol