Correlations between the morphology of diffuse and primitive beta-amyloid (A beta) deposits and the frequency of associated cells in Down's syndrome

被引:29
作者
Armstrong, RA
机构
[1] Vision Sciences, Aston University, Birmingham
[2] Vision Sciences, Aston University
关键词
Down's syndrome; A beta deposits; neurons; glial cells; cortex; hippocampus;
D O I
10.1111/j.1365-2990.1996.tb01131.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Correlations between the morphology of beta-amyloid (A beta) deposits and the frequency with which they are associated with neurons and glial cells were studied in Down's syndrome. The diameter of diffuse deposits was positively correlated with the frequency of large (>25 mu m) neuronal cell bodies in the isocortex and with glial cells in the hippocampus, Diameters of primitive deposits were positively correlated with glial cells in the hippocampus and with glial cells and neurons in the isocortex. Staining intensity was positively correlated with glial cells especially in the hippocampus. The data suggest that: ii) diffuse deposits develop from neurons and primitive deposits from glia; (ii) the size of A beta deposits depends on the numbers of neurons and glia: (iii) glial cells are also involved in the conversion of A beta to amyloid; and (iv) the increased density of primitive deposits in the hippocampus is determined by the high density of glial cells.
引用
收藏
页码:527 / 530
页数:4
相关论文
共 18 条
[1]
EARLY SENILE PLAQUES IN DOWNS-SYNDROME BRAINS SHOW A CLOSE RELATIONSHIP WITH CELL-BODIES OF NEURONS [J].
ALLSOP, D ;
HAGA, SI ;
HAGA, C ;
IKEDA, SI ;
MANN, DMA ;
ISHII, T .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1989, 15 (06) :531-542
[2]
FACTORS DETERMINING THE MORPHOLOGY OF BETA-AMYLOID (A-BETA) DEPOSITS IN DOWNS-SYNDROME [J].
ARMSTRONG, RA .
NEURODEGENERATION, 1995, 4 (02) :179-186
[3]
WHAT DETERMINES THE SIZE FREQUENCY-DISTRIBUTION OF BETA-AMYLOID (A-BETA) DEPOSITS IN ALZHEIMERS-DISEASE PATIENTS [J].
ARMSTRONG, RA ;
MYERS, D ;
SMITH, CUM .
NEUROSCIENCE LETTERS, 1995, 187 (01) :13-16
[4]
EVIDENCE FOR A DIFFUSIONAL MODEL OF ALZHEIMER AMYLOID A4 (BETA-AMYLOID) DEPOSITION DURING NEURITIC PLAQUE-FORMATION [J].
BENES, FM ;
REIFEL, JL ;
MAJOCHA, RE ;
MAROTTA, CA .
NEUROSCIENCE, 1989, 33 (03) :483-488
[5]
THE HUMAN ENTORHINAL CORTEX - NORMAL MORPHOLOGY AND LAMINA-SPECIFIC PATHOLOGY IN VARIOUS DISEASES [J].
BRAAK, H ;
BRAAK, E .
NEUROSCIENCE RESEARCH, 1992, 15 (1-2) :6-31
[6]
BETA-AMYLOID OF ALZHEIMERS-DISEASE INDUCES REACTIVE GLIOSIS THAT INHIBITS AXONAL OUTGROWTH [J].
CANNING, DR ;
MCKEON, RJ ;
DEWITT, DA ;
PERRY, G ;
WUJEK, JR ;
FREDERICKSON, RCA ;
SILVER, J .
EXPERIMENTAL NEUROLOGY, 1993, 124 (02) :289-298
[7]
CRAS P, 1990, AM J PATHOL, V137, P241
[8]
BETA-AMYLOID ACCUMULATION IN AGED CANINE BRAIN - A MODEL OF EARLY PLAQUE-FORMATION IN ALZHEIMERS-DISEASE [J].
CUMMINGS, BJ ;
SU, JH ;
COTMAN, CW ;
WHITE, R ;
RUSSELL, MJ .
NEUROBIOLOGY OF AGING, 1993, 14 (06) :547-560
[9]
SUBTYPES AND DIFFERENTIAL LAMINAR DISTRIBUTIONS OF BETA-A4 DEPOSITS IN ALZHEIMERS-DISEASE - RELATIONSHIP WITH THE INTELLECTUAL STATUS OF 26 CASES [J].
DELAERE, P ;
DUYCKAERTS, C ;
HE, Y ;
PIETTE, F ;
HAUW, JJ .
ACTA NEUROPATHOLOGICA, 1991, 81 (03) :328-335
[10]
REGIONAL DIFFERENCES IN REACTIVE GLIOSIS INDUCED BY SUBSTRATE-BOUND BETA-AMYLOID [J].
HOKE, A ;
CANNING, DR ;
MALEMUD, CJ ;
SILVER, J .
EXPERIMENTAL NEUROLOGY, 1994, 130 (01) :56-66