Butyrylcholinesterase in the life cycle of amyloid plaques

被引:270
作者
Guillozet, AL
Smiley, JF
Mash, DC
Mesulam, MM
机构
[1] Northwestern Univ, Cognit Neurol & Alzheimer Dis Ctr, Sch Med, Chicago, IL 60611 USA
[2] Univ Miami, Sch Med, Dept Neurol, Miami, FL USA
关键词
D O I
10.1002/ana.410420613
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Deposits of diffuse beta-amyloid (A beta) may exist in the brain for many years before leading to neuritic degeneration and dementia. The factors that contribute to the putative transformation of the A beta amyloid from a relatively inert to a pathogenic state remain unknown and may involve interactions with additional plaque constituents. Matching brain sections from 2 demented and 4 nondemented subjects were processed for the demonstration of A beta immunoreactivity, butyrylcholinesterase (BChE) enzyme activity, and thioflavine S binding. Additional sections were processed for the concurrent demonstration of two or three of these markers. A comparative analysis of multiple cytoarchitectonic areas processed with each of these markers indicated that A beta plaque deposits are likely to undergo three stages of maturation, ie, a "diffuse" thioflavine S-negative stage, a thioflavine S-positive (ie, compact) but nonneuritic stage, and a compact neuritic stage. A multiregional analysis showed that BChE-positive plaques were not found in cytoarchitectonic areas or cortical layers that contained only the thioflavine S-negative, diffuse type of A beta plaques. The BChE-positive plaques were found only in areas containing thioflavine S-positive compact plaques, both neuritic and nonneuritic Within such areas, almost all (>98%) BChE-containing plaques bound thioflavine S, and almost all (93%) thioflavine S plaques contained BChE. These results suggest that BChE becomes associated with amyloid plaques at approximately the same time that the A beta deposit assumes a compact beta-pleated conformation. BChE may therefore participate in the transformation of A beta from an initially benign form to an eventually malignant form associated with neuritic tissue degeneration and clinical dementia.
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页码:909 / 918
页数:10
相关论文
共 80 条
[1]   IMMUNOCHEMICAL IDENTIFICATION OF THE SERINE PROTEASE INHIBITOR ALPHA-1-ANTICHYMOTRYPSIN IN THE BRAIN AMYLOID DEPOSITS OF ALZHEIMERS-DISEASE [J].
ABRAHAM, CR ;
SELKOE, DJ ;
POTTER, H .
CELL, 1988, 52 (04) :487-501
[2]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[3]  
Barber K. L., 1996, Society for Neuroscience Abstracts, V22, P1172
[4]   A PEPTIDASE ACTIVITY EXHIBITED BY HUMAN-SERUM PSEUDOCHOLINESTERASE [J].
BOOPATHY, R ;
BALASUBRAMANIAN, AS .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 162 (01) :191-197
[5]  
BURDICK D, 1992, J BIOL CHEM, V267, P546
[6]   EARLY-ONSET ALZHEIMERS-DISEASE CAUSED BY MUTATIONS AT CODON-717 OF THE BETA-AMYLOID PRECURSOR PROTEIN GENE [J].
CHARTIERHARLIN, MC ;
CRAWFORD, F ;
HOULDEN, H ;
WARREN, A ;
HUGHES, D ;
FIDANI, L ;
GOATE, A ;
ROSSOR, M ;
ROQUES, P ;
HARDY, J ;
MULLAN, M .
NATURE, 1991, 353 (6347) :844-846
[7]   SP-40,40 IS A CONSTITUENT OF ALZHEIMERS AMYLOID [J].
CHOIMIURA, NH ;
IHARA, Y ;
FUKUCHI, K ;
TAKEDA, M ;
NAKANO, Y ;
TOBE, T ;
TOMITA, M .
ACTA NEUROPATHOLOGICA, 1992, 83 (03) :260-264
[8]  
Citron M., 1996, Society for Neuroscience Abstracts, V22, P278
[9]   DIFFERENTIAL LAMINAR DISTRIBUTION OF ACETYLCHOLINESTERASE AND BUTYRYLCHOLINESTERASE CONTAINING TANGLES IN THE CEREBRAL-CORTEX OF ALZHEIMERS-DISEASE [J].
COLEMAN, AE ;
GEULA, C ;
PRICE, BH ;
MESULAM, MM .
BRAIN RESEARCH, 1992, 596 (1-2) :340-344
[10]   beta-amyloid deposition and other measures of neuropathology predict cognitive status in Alzheimer's disease [J].
Cummings, BJ ;
Pike, CJ ;
Shankle, R ;
Cotman, CW .
NEUROBIOLOGY OF AGING, 1996, 17 (06) :921-933