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Aberrant Expression of the Glutamate Transporter Excitatory Amino Acid Transporter 1 (EAAT1) in Alzheimer's Disease
- Source :
- The Journal of Neuroscience. 22:RC206-RC206
- Publication Year :
- 2002
- Publisher :
- Society for Neuroscience, 2002.
-
Abstract
- Glutamate-mediated toxicity has been implicated in the neurodegeneration observed in Alzheimer's disease. In particular, glutamate transport dysfunction may increase susceptibility to glutamate toxicity, thereby contributing to neuronal cell injury and death. In this study, we examined the cellular localization of the glial glutamate transporter excitatory amino acid transporter 1 (EAAT1) in the cerebral cortex of control, Alzheimer's disease, and non-Alzheimer dementia cases. We found that EAAT1 was strongly expressed in a subset of cortical pyramidal neurons in dementia cases showing Alzheimer-type pathology. In addition, tau (which is a marker of neurofibrillary pathology) colocalized to those same pyramidal cells that expressed EAAT1. These findings suggest that EAAT1 changes are related to tau expression (and hence neurofibrillary tangle formation) in dementia cases showing Alzheimer-type pathology. This study implicates aberrant glutamate transporter expression as a mechanism involved in neurodegeneration in Alzheimer's disease.
- Subjects :
- Lewy Body Disease
Male
Immunocytochemistry
tau Proteins
Biology
Alzheimer Disease
medicine
Humans
Dementia
Amyotrophic lateral sclerosis
Cellular localization
Aged
Aged, 80 and over
Cerebral Cortex
Pyramidal Cells
General Neuroscience
Neurodegeneration
Glutamate receptor
Neurofibrillary Tangles
Parkinson Disease
Middle Aged
medicine.disease
Immunohistochemistry
Excitatory Amino Acid Transporter 1
Dementia, Multi-Infarct
medicine.anatomical_structure
Cerebral cortex
Toxicity
Female
Neuroscience
Rapid Communication
Biomarkers
Subjects
Details
- ISSN :
- 15292401 and 02706474
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- The Journal of Neuroscience
- Accession number :
- edsair.doi.dedup.....b5ddbff0dbeccba62c17b2bf91c2d0b2
- Full Text :
- https://doi.org/10.1523/jneurosci.22-03-j0004.2002