N-cadherin-based adhesion enhances Abeta release and decreases Abeta42/40 ratio

J Neurochem. 2009 Jan;108(2):350-60. doi: 10.1111/j.1471-4159.2008.05760.x. Epub 2008 Nov 25.

Abstract

In neurons, Presenilin 1(PS1)/gamma-secretase is located at the synapses, bound to N-cadherin. We have previously reported that N-cadherin-mediated cell-cell contact promotes cell-surface expression of PS1/gamma-secretase. We postulated that N-cadherin-mediated trafficking of PS1 might impact synaptic PS1-amyloid precursor protein interactions and Abeta generation. In the present report, we evaluate the effect of N-cadherin-based contacts on Abeta production. We demonstrate that stable expression of N-cadherin in Chinese hamster ovary cells, expressing the Swedish mutant of human amyloid precursor protein leads to enhanced secretion of Abeta in the medium. Moreover, N-cadherin expression decreased Abeta(42/40) ratio. The effect of N-cadherin expression on Abeta production was accompanied by the enhanced accessibility of PS1/gamma-secretase to amyloid precursor protein as well as a conformational change of PS1, as demonstrated by the fluorescence lifetime imaging technique. These results indicate that N-cadherin-mediated synaptic adhesion may modulate Abeta secretion as well as the Abeta(42/40) ratio via PS1/N-cadherin interactions.

Publication types

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

MeSH terms

  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Antigens, CD / chemistry
  • Antigens, CD / genetics
  • Antigens, CD / physiology*
  • Cadherins / chemistry
  • Cadherins / genetics
  • Cadherins / physiology*
  • Cells, Cultured
  • Cricetinae
  • Cricetulus
  • Culture Media, Serum-Free / pharmacology
  • Embryo, Mammalian
  • Extracellular Fluid / drug effects
  • Extracellular Fluid / metabolism
  • Gene Expression / physiology
  • Gene Expression Regulation / genetics
  • Hippocampus / cytology
  • Humans
  • Mutation / genetics
  • Neurons / metabolism
  • Peptide Fragments / metabolism*
  • Presenilin-1 / genetics
  • Presenilin-1 / metabolism
  • Rats
  • Structure-Activity Relationship
  • Transfection / methods
  • Trichothecenes / metabolism

Substances

  • Amyloid beta-Peptides
  • Antigens, CD
  • CDH2 protein, human
  • Cadherins
  • Culture Media, Serum-Free
  • Peptide Fragments
  • Presenilin-1
  • Trichothecenes
  • amyloid beta-protein (1-40)
  • amyloid beta-protein (1-42)
  • baccharin