Abstract |
An immunohistochemical study focusing on glial cells was performed using monoclonal antibodies against microtubule-associated proteins (MAP1, MAP2 and MAP5), transferrin, leukocyte common antigen (LCA) and glial fibrillary acidic protein (GFAP) in 5 cases of multiple system atrophy (MSA) exhibiting olivopontocerebellar atrophy and striatonigral degeneration. An antibody to MAP5, a fetal antigen in developing brain, was strongly demonstrated in the glial cytoplasmic inclusions (GCIs) which have recently drawn a great deal of attention and were observed in all 5 cases of MSA. Moreover, MAP5-positive glial cells (MAP5-Gs) were present in significantly higher number than in the controls in various regions where GCIs were found, predominantly in putamen, substantia nigra, cerebellar white matter and internal capsule. LCA and transferrin, markers of microglia and oligodendroglia, respectively, were immunohistochemically detected in some MAP5-Gs. GFAP, on the other hand, was not expressed in MAP5-Gs at all. These findings suggest that MAP5-Gs consist of reactive microglia and oligodendroglia. Our study is the first to demonstrate immunohistochemical detection of MAP5 in glial pathological changes in MSA.
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Authors | N Arai, M Nishimura, M Oda, Y Morimatsu, R Ohe, H Nagatomo |
Journal | Journal of the neurological sciences
(J Neurol Sci)
Vol. 109
Issue 1
Pg. 102-6
(May 1992)
ISSN: 0022-510X [Print] Netherlands |
PMID | 1517758
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Biomarkers
- Microtubule-Associated Proteins
- Nerve Tissue Proteins
- Transferrin
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Topics |
- Aged
- Atrophy
- Biomarkers
- Brain Chemistry
- Corpus Striatum
(chemistry, pathology)
- Female
- Gene Expression
- Humans
- Macrophages
(metabolism, pathology)
- Male
- Microtubule-Associated Proteins
(biosynthesis)
- Middle Aged
- Neoplasms
(metabolism)
- Nerve Degeneration
- Nerve Tissue Proteins
(biosynthesis)
- Oligodendroglia
(metabolism, pathology)
- Olivopontocerebellar Atrophies
(metabolism, pathology)
- Pneumonia
(metabolism)
- Shy-Drager Syndrome
(metabolism, pathology)
- Substantia Nigra
(chemistry, pathology)
- Transferrin
(analysis)
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