QUANTITATION OF ALZHEIMERS AMYLOID PEPTIDE AND IDENTIFICATION OF RELATED AMYLOID PROTEINS BY DOT-BLOT IMMUNOASSAY

被引:22
作者
PERMANNE, B
BUEE, L
DAVID, JP
FALLETBIANCO, C
DIMENZA, C
DELACOURTE, A
机构
[1] INSERM,U422,F-59045 LILLE,FRANCE
[2] HOP EMILE ROUX,F-94450 LIMEIL BREVANNES,FRANCE
关键词
AGING; AMYLOIDOSIS; APOLIPOPROTEIN E; NEUROPATHOLOGY; PROTEOGLYCANS;
D O I
10.1016/0006-8993(95)00431-O
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In Alzheimer's disease, the main component of amyloid deposits is a 39-43 amino acid peptide referred to as amyloid peptide or A beta. A crucial issue in the study of this disorder is to define the sequence of events that lead to amyloid deposition. In the present study, a new approach was developed that allows to specifically solubilize A beta peptide trapped within amyloid deposits and to quantify its amount by dot-blot immunoassay. The present method also permits to isolate components tightly bound to A beta and that are likely to catalyze its aggregation. Biochemical A beta quantitation was performed in 4 Brodmann areas from 17 elderly individuals exhibiting different degrees of amyloidosis. In parallel, classical neuropathology was done by histochemical and immunohistochemical methods. A beta amounts (pmol) were correlated to the number of amyloid deposits determined by neuropathology showing high statistical significance. Moreover, amyloid-binding proteins including apolipoprotein E and heparan sulfate proteoglycans were also found associated to A beta in the amyloid preparation. The present biochemical procedure is a new and reliable method to quantify amyloid deposition in brain. Furthermore, it allows to detect amyloid-associated components such as apolipoprotein E, that may be involved in the pathological process of amyloidogenesis.
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页码:154 / 162
页数:9
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