Acetylcholinesterase is increased in the brains of transgenic mice expressing the C-terminal fragment (CT100) of the beta-amyloid protein precursor of Alzheimer's disease

J Neurochem. 1998 Aug;71(2):723-31. doi: 10.1046/j.1471-4159.1998.71020723.x.


Acetylcholinesterase (AChE) expression is markedly affected in Alzheimer's disease (AD). AChE activity is lower in most regions of the AD brain, but it is increased within and around amyloid plaques. We have previously shown that AChE expression in P19 cells is increased by the amyloid beta protein (A beta). The aim of this study was to investigate AChE expression using a transgenic mouse model of A beta overproduction. The beta-actin promoter was used to drive expression of a transgene encoding the 100-amino acid C-terminal fragment of the human amyloid precursor protein (APP CT100). Analysis of extracts from transgenic mice revealed that the human sequences of full-length human APP CT100 and A beta were overexpressed in the brain. Levels of salt-extractable AChE isoforms were increased in the brains of APP CT100 mice. There was also an increase in amphiphilic monomeric form (G1A) of AChE in the APP CT100 mice, whereas other isoforms were not changed. An increase in the proportion of G1A AChE was also detected in samples of frontal cortex from AD patients. Analysis of AChE by lectin binding revealed differences in the glycosylation pattern in APP CT100 mice similar to those observed in frontal cortex samples from AD. The results are consistent with the possibility that changes in AChE isoform levels and glycosylation patterns in the AD brain may be a direct consequence of altered APP metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / metabolism*
  • Amyloid beta-Protein Precursor / genetics*
  • Animals
  • Butyrylcholinesterase / metabolism
  • Cerebral Cortex / cytology
  • Cerebral Cortex / enzymology
  • Choline O-Acetyltransferase / metabolism
  • Down Syndrome / metabolism
  • Gene Expression / physiology
  • Glycosylation
  • Humans
  • Isoenzymes / metabolism
  • Mice
  • Mice, Transgenic / metabolism*
  • Middle Aged
  • Neurons / enzymology
  • Peptide Fragments / genetics*
  • Substrate Specificity


  • Amyloid beta-Protein Precursor
  • Isoenzymes
  • Peptide Fragments
  • amyloid precursor protein, carboxy-terminal 100 residues
  • Choline O-Acetyltransferase
  • Acetylcholinesterase
  • Butyrylcholinesterase