Overexpression of wild type but not an FAD mutant presenilin-1 promotes neurogenesis in the hippocampus of adult mice

Neurobiol Dis. 2002 Jun;10(1):8-19. doi: 10.1006/nbdi.2002.0490.

Abstract

Mutations in the presenilin-1 (PS-1) gene are one cause of familial Alzheimer's disease (FAD). However, the functions of the PS-1 protein as well as how PS-1 mutations cause FAD are incompletely understood. Here we investigated if neuronal overexpression of wild-type or FAD mutant PS-1 in transgenic mice affects neurogenesis in the hippocampus of adult animals. We show that either a wild-type or an FAD mutant PS-1 transgene reduces the number of neural progenitors in the dentate gyrus. However, the wild-type, but not the FAD mutant PS-1 promoted the survival and differentiation of progenitors leading to more immature granule cell neurons being generated in PS-1 wild type expressing animals. These studies suggest that PS-1 plays a role in regulating neurogenesis in adult hippocampus and that FAD mutants may have deleterious properties independent of their effects on amyloid deposition.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging / genetics
  • Aging / physiology
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / metabolism
  • Animals
  • Cell Count
  • Cell Differentiation / genetics
  • Cell Survival / genetics
  • Hippocampus / cytology*
  • Hippocampus / growth & development
  • Hippocampus / physiology*
  • Humans
  • Membrane Proteins / biosynthesis*
  • Membrane Proteins / genetics*
  • Membrane Proteins / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Mice, Transgenic
  • Mutation / physiology*
  • Neurons / cytology*
  • Neurons / metabolism
  • Neurons / physiology*
  • Presenilin-1
  • Stem Cells / cytology

Substances

  • Membrane Proteins
  • PSEN1 protein, human
  • Presenilin-1