LSD1 protects against hippocampal and cortical neurodegeneration

Nat Commun. 2017 Oct 9;8(1):805. doi: 10.1038/s41467-017-00922-9.

Abstract

To investigate the mechanisms that maintain differentiated cells, here we inducibly delete the histone demethylase LSD1/KDM1A in adult mice. Loss of LSD1 leads to paralysis, along with widespread hippocampus and cortex neurodegeneration, and learning and memory defects. We focus on the hippocampus neuronal cell death, as well as the potential link between LSD1 and human neurodegenerative disease and find that loss of LSD1 induces transcription changes in common neurodegeneration pathways, along with the re-activation of stem cell genes, in the degenerating hippocampus. These data implicate LSD1 in the prevention of neurodegeneration via the inhibition of inappropriate transcription. Surprisingly, we also find that transcriptional changes in the hippocampus are similar to Alzheimer's disease (AD) and frontotemporal dementia (FTD) cases, and LSD1 is specifically mislocalized to pathological protein aggregates in these cases. These data raise the possibility that pathological aggregation could compromise the function of LSD1 in AD and FTD."LSD1 is a histone demethylase that plays many roles during development. Here, the authors provide evidence that loss of LSD1 in adult mice leads to paralysis and neurodegeneration in the hippocampus and cortex and suggest a potential link between LSD1 and human neurodegenerative disease.

Publication types

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

MeSH terms

  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Animals
  • Case-Control Studies
  • Cell Differentiation
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology*
  • DNA-Binding Proteins / metabolism
  • Frontotemporal Dementia / metabolism
  • Frontotemporal Dementia / pathology
  • Gene Expression Regulation
  • Hippocampus / metabolism
  • Hippocampus / pathology*
  • Histone Demethylases / genetics*
  • Histone Demethylases / metabolism*
  • Humans
  • Memory Disorders / genetics
  • Memory Disorders / pathology
  • Mice, Transgenic
  • Motor Neurons
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / pathology
  • Stem Cells / pathology
  • Stem Cells / physiology
  • tau Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • MAPT protein, human
  • TARDBP protein, human
  • tau Proteins
  • Histone Demethylases
  • KDM1a protein, mouse
  • KDM1A protein, human