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 |
Keywords
- Acetylcholinesterase
- Alzheimer's disease
- Cerebral cortex
- Cytoskeleton
- Development
- Human brain
- Neurofilament protein
- SMI-32
ASJC Scopus subject areas
- Neuroscience(all)
- Molecular Biology
- Clinical Neurology
- Developmental Biology