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PMID: 7778678 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Widespread cytoskeletal pathology characterizes corticobasal degeneration.

The American journal of pathology ·Vol. 146 ·No. 6 ·1995-06-00 ·Pages 1388-96

Feany MB, Dickson DW

Abstract

Corticobasal degeneration (CBD) is a rare, progressive neurological disorder characterized by widespread neuronal and glial pathology. Using immunohistochemistry and laser confocal microscopy, we demonstrate that the nonamyloid cortical plaques of CBD are actually collections of abnormal tau in the distal processes of astrocytes. These glial cells express both vimentin and CD44, markers of astrocyte activation. Glial pathology also includes tau-positive cytoplasmic inclusions, here localized to Leu 7-expressing oligodendrocytes. In addition, a wide array of neuronal pathology is defined with tau-positive inclusions in multiple domains of a variety of cortical neurons. CBD thus exhibits widespread glial and neuronal cytoskeletal pathology, including a novel structure, the astrocytic plaque. CBD is a disease of generalized cytoskeletal disruption affecting several cell types and multiple domains of these cells. The further definition of CBD pathology refines the diagnosis and pathophysiological understanding of this unique disease and has important implications for other neurodegenerative diseases, like Alzheimer's disease, characterized by abnormal tau deposition.

MeSH Terms
Aged Aged, 80 and over Basal Ganglia Diseases/pathology Cytoskeleton/pathology Female Humans Immunoenzyme Techniques Male Nerve Degeneration/physiology Oligodendroglia/chemistry tau Proteins/analysis
Chemicals
tau Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Feany M B
Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Dickson D W
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Article Info
Journal
The American journal of pathology
Abbr.
Am J Pathol
ISSN
0002-9440
Published
1995-06-00
Pages
1388-96
Language
English
Region
United States
NLM ID
0370502
PMCID
PMC1870913
Subset
IM
Grants
NIA NIH HHS · AG06803 · United States
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