Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic β-amyloid pathology known as 'cotton wool' plaques

被引:35
|
作者
Mann, DMA
Takeuchi, A
Sato, S
Cairns, NJ
Lantos, PL
Rossor, MN
Haltia, M
Kalimo, H
Iwatsubo, T
机构
[1] Univ Manchester, Dept Med, Clin Neurosci Res Grp, Manchester M13 9PT, Lancs, England
[2] Univ Tokyo, Dept Neuropathol & Neurosci, Tokyo, Japan
[3] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Tokyo, Japan
[4] Inst Psychiat, Dept Neuropathol, Brain Bank, London SE5 8AF, England
[5] UCL Natl Hosp Neurol & Neurosurg, Dept Neurol, London WC1N 3BG, England
[6] Univ Helsinki, Dept Pathol, Helsinki, Finland
[7] Univ Helsinki, Cent Hosp, Helsinki, Finland
[8] Univ Turku, Dept Pathol, Turku, Finland
关键词
Alzheimer's disease; beta-amyloid; mutation; presenilin-1; gene; senile plaque;
D O I
10.1046/j.1365-2990.2001.00316.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The pattern of deposition of amyloid beta protein (A beta) was investigated, using the monoclonal antibodies BA27 and BC05 detecting the C-terminal species A beta (40) and A beta (42(43)), in six cases of Alzheimer's disease (AD) due to deletions in exon 9 of PS-1 gene. These cases are characterized histologically by the presence of very large rounded plaques within the frontal cortex, known as 'cotton wool' plaques, composed of both A beta (40) and A beta (42(43)) that are relatively free from neuritic changes and glial cell components, and usually devoid of a compact amyloid core. In the cerebellum the plaques are almost entirely of a compact type, again composed of A beta (40) and A beta (42(43)), with only few diffuse A beta (42(43)) containing plaques. The area fraction of A beta (40), and the ratio between A beta (40) and A beta (42(43)), in frontal cortex was significantly higher than that seen in other cases of AD due to different PS-1 mutations, or in cases of sporadic AD, all of similar APO E genotype. The area fractions of A beta (42(43)), however, did not significantly differ between these three groups. The unusual nature of the A beta deposition in these cases may reflect the uniqueness of the mutation, which results in a failure to constitutively cleave the PS-1 holoprotein into its active form, and the effect this might have on APP trafficking and catabolism.
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收藏
页码:189 / 196
页数:8
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