REST and stress resistance in ageing and Alzheimer's disease

Nature. 2014 Mar 27;507(7493):448-54. doi: 10.1038/nature13163. Epub 2014 Mar 19.

Abstract

Human neurons are functional over an entire lifetime, yet the mechanisms that preserve function and protect against neurodegeneration during ageing are unknown. Here we show that induction of the repressor element 1-silencing transcription factor (REST; also known as neuron-restrictive silencer factor, NRSF) is a universal feature of normal ageing in human cortical and hippocampal neurons. REST is lost, however, in mild cognitive impairment and Alzheimer's disease. Chromatin immunoprecipitation with deep sequencing and expression analysis show that REST represses genes that promote cell death and Alzheimer's disease pathology, and induces the expression of stress response genes. Moreover, REST potently protects neurons from oxidative stress and amyloid β-protein toxicity, and conditional deletion of REST in the mouse brain leads to age-related neurodegeneration. A functional orthologue of REST, Caenorhabditis elegans SPR-4, also protects against oxidative stress and amyloid β-protein toxicity. During normal ageing, REST is induced in part by cell non-autonomous Wnt signalling. However, in Alzheimer's disease, frontotemporal dementia and dementia with Lewy bodies, REST is lost from the nucleus and appears in autophagosomes together with pathological misfolded proteins. Finally, REST levels during ageing are closely correlated with cognitive preservation and longevity. Thus, the activation state of REST may distinguish neuroprotection from neurodegeneration in the ageing brain.

Publication types

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

MeSH terms

  • Aged
  • Aged, 80 and over
  • Aging / genetics
  • Aging / metabolism*
  • Aging / pathology
  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Amyloid beta-Peptides / antagonists & inhibitors
  • Amyloid beta-Peptides / toxicity
  • Animals
  • Autophagy
  • Brain / cytology
  • Brain / metabolism
  • Brain / pathology
  • Caenorhabditis elegans Proteins / metabolism
  • Cell Death / genetics
  • Cell Nucleus / metabolism
  • Chromatin Immunoprecipitation
  • Cognition
  • Cognitive Dysfunction / metabolism
  • DNA-Binding Proteins / metabolism
  • Down-Regulation
  • Frontotemporal Dementia / metabolism
  • Frontotemporal Dementia / pathology
  • Gene Expression Regulation
  • Humans
  • Lewy Body Disease / metabolism
  • Lewy Body Disease / pathology
  • Longevity
  • Mice
  • Neurons / cytology
  • Neurons / metabolism
  • Neurons / pathology
  • Neuroprotective Agents / metabolism
  • Oxidative Stress* / genetics
  • Oxidative Stress* / physiology
  • Phagosomes
  • Repressor Proteins / deficiency
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Transcription Factors / metabolism
  • Up-Regulation
  • Wnt Signaling Pathway
  • Young Adult

Substances

  • Amyloid beta-Peptides
  • Caenorhabditis elegans Proteins
  • DNA-Binding Proteins
  • Neuroprotective Agents
  • RE1-silencing transcription factor
  • Repressor Proteins
  • SPR-4 protein, C elegans
  • Transcription Factors

Associated data

  • GEO/GSE53890