Cellular stress/the unfolded protein response: relevance to sleep and sleep disorders

Sleep Med Rev. 2009 Jun;13(3):195-204. doi: 10.1016/j.smrv.2009.01.001. Epub 2009 Mar 28.

Abstract

Recent transcript profiling and microarray studies are beginning to unveil some of the mysteries of sleep. One of the most important clues has been the identification of the endoplasmic reticulum (ER) resident chaperone, immunoglobulin binding protein (BiP), that increases with sleep deprivation in all species studied. BiP, an ER resident chaperone, is the key cellular marker and master regulator of a signaling pathway called the ER stress response or unfolded protein response. The ER stress response occurs in 3 phases. It is healthy, protective and adaptive when the ER stress is moderate. Failure of the adaptive response leads to the activation of an inflammatory response. When the ER stress burden is great and prolonged, executioner pathways are activated. Collectively this work provides new evidence that modest sleep deprivation induces cellular stress that activates an adaptive response. Aging tilts the response to sleep deprivation from one that is adaptive and protective to one that is maladaptive. Understanding the pathways activated by sleep loss and the mechanisms by which they occur will allow the development of therapies to protect the brain during prolonged wakefulness and specifically in sleep disorders including those associated with aging.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Activating Transcription Factor 6 / genetics
  • Activating Transcription Factor 6 / metabolism
  • Adaptation, Physiological / physiology
  • Aging / physiology
  • Apoptosis / physiology
  • Brain / physiopathology
  • Caspases / genetics
  • Endoplasmic Reticulum / physiology
  • Endoplasmic Reticulum Chaperone BiP
  • Endoribonucleases / genetics
  • Endoribonucleases / metabolism
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism
  • Heat-Shock Proteins / physiology*
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Motor Neurons / physiology
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Protein Array Analysis
  • Protein Biosynthesis
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Transport
  • Signal Transduction / physiology
  • Sleep Deprivation / genetics
  • Sleep Deprivation / metabolism
  • Sleep Deprivation / physiopathology
  • Sleep Wake Disorders / genetics
  • Sleep Wake Disorders / metabolism
  • Sleep Wake Disorders / physiopathology*
  • Wakefulness / physiology
  • eIF-2 Kinase / genetics
  • eIF-2 Kinase / metabolism

Substances

  • ATF6 protein, human
  • Activating Transcription Factor 6
  • Endoplasmic Reticulum Chaperone BiP
  • Heat-Shock Proteins
  • Membrane Proteins
  • NF-kappa B
  • ERN2 protein, human
  • PERK kinase
  • Protein Serine-Threonine Kinases
  • eIF-2 Kinase
  • Endoribonucleases
  • Caspases