Evidence for axonal loss in regions occupied by senile plaques in Alzheimer cortex
Abstract
The studies described have sought to determine what, if any, relationship exists between axons and the senile plaque, a hallmark histopathological feature of Alzheimer's disease. A double stain was performed on both early and late Alzheimer frontal cortex tissues in order to examine the interaction between axons stained with antibodies against the 200,000 mol. wt neurofilament subunit (NFP-200) of the axon cytoskeleton and Thioflavin-S, a fluorescent dye that stains plaques. Serial photomicrographs of plaques were taken and axon and plaque profiles were three-dimensionally reconstructed. Analysis of computer-processed images revealed that there were fewer axons within plaques than in regions lying one and two plaque distances away. When axons were observed passing through plaques, swelling and disruption of normal morphology was frequently present. Statistical analyses of axon counts within and around placques showed a gradient of axon density, with increased numbers occurring at progressive distances from the placque. Similar patterns were seen for early and late stages of the disease. The results of this study indicate that disruption of the axonal cytoskeleton may occur within the regions occupied by plaques.
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The magnitude of DTI white matter alterations correlates with cognitive performance, making white matter damage a likely contributor to AD symptoms.
“The magnitude of DTI WM alterations correlates with cognitive performance, making WM damage a likely contributor to the symptoms experienced by patients and key to understanding AD pathophysiology3.”
From Amyloid-beta induced retrograde axonal degeneration in a mouse tauopathy model (2019) · cites this paper as [3]
Cites
Pathogenesis of Neuritic (Senile) and Amyloid Plaque Formation
Wisniewski, H. M., Vorbrodt, A. W., Moretz, R. C., Lossinsky, A. S., & Grundke-Iqbal, I. (1982) · Experimental Brain Research Supplementum · doi:10.1007/978-3-642-68507-1_1 · Cited by 45 · see citing works
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Emerging principles of altered neural circuitry in schizophrenia
Benes, F. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00041-7 · Cited by 513 · see citing works
Self-citationThe cause of neuronal degeneration in Alzheimer’s disease
Vickers, J. (2000) · Progress in Neurobiology · doi:10.1016/s0301-0082(99)00023-4 · Cited by 254 · see citing works
Amyloid-beta induced retrograde axonal degeneration in a mouse tauopathy model
Nishioka, C., Liang, H.-F., Barsamian, B., & Sun, S.-W. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.007 · Cited by 30 · see citing works
- Authors
- Benes, F. M., Farol, P. A., Majocha, R. E., Marotta, C. A., & Bird, E. D.
- Affiliations
- Harvard University (US)
- McLean Hospital (US)
- Corresponding author
- Benes, F.M.
- ORCID
- Benes, F.M.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1991-01
- Volume
- 42
- Issue
- 3
- Pages
- 651-660
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2037096800
- Cited by
- 40
- References
- 1
- Citations by year
- 2020: 2 · 2019: 2 · 2018: 3 · 2017: 2 · 2015: 2 · 2013: 2 · 2012: 1
- FWCI
- 1.93
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5p01ag002126-11)
- National Institute on Aging (AG 02126)
- National Institute of Mental Health (MH.NS 31862, MH00423)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Alzheimer's disease, amyloid plaques, axonal loss, axon cytoskeleton, neurofilament subunits, thioflavin S, frontal cortex, axonal swellings, axonal disruption
- MeSH terms
- Alzheimer Disease, Amyloid, Axons, Cytoskeleton, Fluorescent Antibody Technique, Fluorescent Dyes, Frontal Lobe, Humans, Image Processing, Computer-Assisted, Nerve Tissue Proteins, Thiazoles, Neurofilament Proteins, Benzothiazoles
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