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The Journal of Neuroscience, April 1, 1999, 19(7):2706-2716
Reorganization of Cholinergic Terminals in the Cerebral Cortex
and Hippocampus in Transgenic Mice Carrying Mutated Presenilin-1 and
Amyloid Precursor Protein Transgenes
Tak Pan
Wong1,
Thomas
Debeir1,
Karen
Duff2, and
A. Claudio
Cuello1
1 Department of Pharmacology and Therapeutics, McGill
University, Montreal, Quebec, Canada, H3G 1Y6, and 2
Nathan Kline Institute, Orangeburg, New York 10962
Cholinergic deficits are one of the most consistent
neuropathological landmarks in Alzheimer's disease (AD). We have
examined transgenic mouse models (PS1M146L,
APPK670N,M671L) and a doubly transgenic line
(APPK670N,M671L + PS1M146L) that
overexpress mutated AD-related genes [presenilin-1 (PS1) and the
amyloid precursor protein (APP)] to investigate the effect of
AD-related gene overexpression and/or amyloidosis on cholinergic parameters.
The size of the basal forebrain cholinergic neurons and the pattern of
cholinergic synapses in the hippocampus and cerebral cortex were
revealed by immunohistochemical staining for choline acetyltransferase
and the vesicular acetylcholine transporter, respectively. At
the time point studied (8 months), no apparent changes in either the
size or density of cholinergic synapses were found in the
PS1M146L mutant relative to the nontransgenic controls.
However, the APPK670N,M671L mutant showed a significant elevation in the density of cholinergic synapses in the frontal and
parietal cortices. Most importantly, the double mutant
(APPK670N,M671L + PS1M146L), which had
extensive amyloidosis, demonstrated a prominent diminution in the
density of cholinergic synapses in the frontal cortex and a reduction
in the size of these synapses in the frontal cortex and hippocampus.
Nonetheless, no significant changes in the size of basal forebrain
cholinergic neurons were observed in these three mutants. This study
shows a novel role of APP and a synergistic effect of APP and PS1 that
correlates with amyloid load on the reorganization of the cholinergic
network in the cerebral cortex and hippocampus at the time point studied.
Key words:
Alzheimer's disease; cholinergic synapse; amyloid
precursor protein; presenilin-1; transgenic mice; vesicular
acetylcholine transporter
Copyright © 1999 Society for Neuroscience 0270-6474/99/1972706-11$05.00/0
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