Amyloid precursor protein increases cortical neuron size in transgenic mice

Neurobiol Aging. 2009 Aug;30(8):1238-44. doi: 10.1016/j.neurobiolaging.2007.12.024. Epub 2008 Mar 4.

Abstract

The amyloid precursor protein (APP) is the source of beta-amyloid, a pivotal peptide in the pathogenesis of Alzheimer's disease (AD). This study examines the possible effect of APP transgene expression on neuronal size by measuring the volumes of cortical neurons (microm(3)) in transgenic mouse models with familial AD Swedish mutation (APPswe), with or without mutated presenilin1 (PS1dE9), as well as in mice carrying wild-type APP (APPwt). Overexpression of APPswe and APPwt protein, but not of PS1dE9 alone, resulted in a greater percentage of medium-sized neurons and a proportionate decrease in the percentage of small-sized neurons. Our observations indicate that the overexpression of mutant (APPswe) or wild-type APP in transgenic mice is necessary and sufficient for hypertrophy of cortical neurons. This is highly suggestive of a neurotrophic effect and also raises the possibility that the lack of neuronal loss in transgenic mouse models of AD may be attributed to overexpression of APP.

Publication types

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

MeSH terms

  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism*
  • Analysis of Variance
  • Animals
  • Cell Size*
  • Cerebral Cortex / cytology*
  • Cerebral Cortex / metabolism
  • Female
  • Male
  • Mice
  • Mice, Transgenic
  • Mutation
  • Neurons / cytology*
  • Neurons / metabolism
  • Presenilin-1 / genetics
  • Presenilin-1 / metabolism
  • Protease Nexins
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*
  • Sex Characteristics

Substances

  • Amyloid beta-Protein Precursor
  • Presenilin-1
  • Protease Nexins
  • Receptors, Cell Surface