Abstract
The majority of acetylcholinesterase-rich pyramidal neurons in neocortical layers III and V of the human brain displayed intense immunostaining with SMI-32, a monoclonal antibody which recognizes a non-phosphorylated epitope of neurofilament proteins. In contrast, very few of the heteromorphic acetylcholinesterase-rich perikarya embedded in the white matter of the cerebral hemispheres are associated with this type of immunostaining. These two groups of acetylcholinesterase-rich cortical neurons can thus be differentiated not only on the basis of morphology and location but also on the basis of cytochemical signature. The concurrent visualization of SMI-32 immunoreactivity and acetylcholinesterase enzyme activity also showed that SMI-32 immunoreactive neurons can be subdivided into several subgroups on the basis of their perikaryal acetylcholinesterase activity.
Original language | English (US) |
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Pages (from-to) | 169-173 |
Number of pages | 5 |
Journal | Brain research |
Volume | 544 |
Issue number | 1 |
DOIs | |
State | Published - Mar 22 1991 |
Funding
Supported m part by a Jav~ts Neurosc~ence Invesugator Award (NS20285), Alzheimer's Disease Research Center Grant (AG05134), the Alzheimer's Disease and Related Disorders Association, an NRSA Fellowship Award (AG05455), NS18IT0 and NS25785 Leah Christie, Knstin Bouve and Annemane Dineen provided expert secretarml and techmcal assistance
Keywords
- Acetylcholinesterase
- Alzheimer's disease
- Cerebral cortex
- Cytoskeleton
- Development
- Human brain
- Neurofilament protein
- SMI-32
ASJC Scopus subject areas
- Clinical Neurology
- Molecular Biology
- General Neuroscience
- Developmental Biology