Astrocytes degenerate in frontotemporal dementia: possible relation to hypoperfusion

被引:61
作者
Martin, JA [1 ]
Craft, DK
Su, JH
Kim, RC
Cotman, CW
机构
[1] Univ Calif Irvine, Alzheimers Dis Res Ctr, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Pathol, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
关键词
frontotemporal dementia; degeneration; astrogliosis; GFAP; TdT; confocal imaging; SPECT; hypoperfusion;
D O I
10.1016/S0197-4580(00)00231-1
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
To understand the extent and specificity of astrocyte pathology in sporadic frontotemporal dementia (FTD), we examined several FTD cases for molecular and morphologic characteristics of astrocyte degeneration. We quantified reactive and degenerating astrocytes in sections of frontal, temporal, parietal, and occipital cortex identified using glial fibrillary acidic protein (GFAP) immunoreactivity, terminal deoxynucleotidyl transferase (TdT) labeling, and morphological characteristics and compared them with nondemented, age-matched control brains. Conventional and confocal microscopy revealed that a subpopulation of GFAP(+) astrocytes exhibited positive TdT labeling and beading of their processes in the frontal, temporal, and parietal cortices in 5 of 7 FTD cases that also exhibited gliosis. This morphology was reproduced in cultured astrocytes using ischemic insults. Degenerating astrocytes in FTD correlated inversely with cerebral blood flow as measured by single photon emission computed tomography (SPECT) analysis of Xe-133 inhalation (r = 0.55, p < 0.05). Furthermore, areas of significant astrogliosis corresponded to areas of SPECT hypoperfusion, suggesting that astrocytes may be affected by or perhaps have a causal role in the disturbances of cerebral perfusion in FTD. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:195 / 207
页数:13
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