Abnormal glial cytoskeleton in progressive supranuclear palsy

被引：9

作者：

Amano, N

Takahashi, T

Yagishita, S

Inoue, M

Matsushita, M

机构：

[1] UNIV TOKYO,FAC MED,DEPT PSYCHIAT,TOKYO 113,JAPAN

[2] KANAGAWA REHABIL CTR,DEPT NEUROPSYCHIAT,KANAGAWA,JAPAN

[3] KANAGAWA REHABIL CTR,DEPT PATHOL,KANAGAWA,JAPAN

来源：

NEUROPATHOLOGY | 1996年 / 16卷 / 02期

关键词：

abnormal glial cytoskeleton; argyrophilic thread; glial coiled body; neuropathology; progressive supranuclear palsy;

D O I：

10.1111/j.1440-1789.1996.tb00169.x

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Progressive supranuclear palsy (PSP) is characterized by neurodegenerative changes of the basal ganglia, brainstem and the cerebellum. Moreover, it is noteworthy that abnormal cytoskeleton of glial cells is distributed widely in the brain. The morphological, immunohistochemical and ultrastructural properties of the peculiar glia have been elucidated, However, many factors remain unsettled regarding the abnormalities. The purpose of this paper is to define the properties of PSP, to present its distributional characteristics, and to examine the correlation of PSP with neuronal loss and astrocytosis.

引用

页码：139 / 144

页数：6

共 15 条

[1]

AMANO N, 1989, Brain and Nerve (Tokyo), V41, P35

[2]

AMANO N, 1993, JPN J GERIATR PSYCHI, V4, P1129

[3]

AMANO N, 1994, DEMENTIA, V8, P94

[4] SILVER IMPREGNATION OF ALZHEIMER NEUROFIBRILLARY CHANGES COUNTERSTAINED FOR BASOPHILIC MATERIAL AND LIPOFUSCIN PIGMENT [J].