Reactive astrocytes are widespread in the cortical gray matter of amyotrophic lateral sclerosis
- 15 June 1994
- journal article
- research article
- Published by Wiley in Journal of Neuroscience Research
- Vol. 38 (3), 336-347
- https://doi.org/10.1002/jnr.490380312
Abstract
The distribution of reactive astrocytes was examined in the cortical gray matter of non-motor and motor regions from cases of familial and sporadic amyotrophic lateral sclerosis (ALS) and compared to that of β-amyloid deposits. By glial fibrillary acidic protein immunocytochemistry, patches of reactive astrocytes, characterized by multiple reactive astrocytes in a circular or patch-like formation, occurred in 12 of 15 ALS cases examined. These patches of reactive astrocytes were not restricted to the motor cortex but were found in the gray matter in ALS in all examined brain regions, including frontal, temporal, inferior parietal, cingulate, occipital, and motor cortices, from both familial and sporadic ALS cases. Reactive astrocytes were also found in the subpial region and at the gray/white matter junction. Because patches of astrocytes can occur in association with senile plaques, β-amyloid was localized. By immunostaining, β-amyloid deposits were observed in five of the 15 ALS cases: three cases had only early plaques, two had both early and classic plaques. The number of ALS cases with both astrocyte patches and amyloid plaques was four of 15, but typically astrocyte patches in ALS occurred without any evidence of an association with β-amyloid deposits. Therefore, the astrocyte patches in ALS are not the result of β-amyloid deposition. The widespread occurrence of reactive astrocytes, as patches in the cortical gray matter and in the subpial region and at the gray/white matter junction, is evidence of a widespread pathology in ALS cortex in both familial and sporadic forms of the disease.Keywords
This publication has 34 references indexed in Scilit:
- Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide DismutaseScience, 1993
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- Glial fibrillary acidic protein and βA4 protein deposits in temporal lobe of aging brain and senile dementia of the Alzheimer type: Relation with the cognitive state and with quantitative studies of senile plaques and neurofibrillary tanglesJournal of Neuroscience Research, 1990
- Patterns of gliosis in alzheimer's disease and aging cerebrumGlia, 1989
- The neuroexcitotoxic amino acids glutamate and aspartate are altered in the spinal cord and brain in amyotrophic lateral sclerosisAnnals of Neurology, 1988
- Cortical Motor-Sensory Hypometabolism in Amyotrophic Lateral SclerosisJournal of Computer Assisted Tomography, 1988
- Lowered cerebral glucose utilization in amyotrophic lateral sclerosisAnnals of Neurology, 1987
- Ganglioside patterns in amyotrophic lateral sclerosis brain regionsAnnals of Neurology, 1985
- Dementia and motor neuron disease: Morphometric, biochemical, and Golgi studiesAnnals of Neurology, 1984
- Degeneration of the human Betz cell due to amyotrophic lateral sclerosisExperimental Neurology, 1979