Neuropil threads of Alzheimer's disease show a marked alteration of the normal cytoskeleton
Open accessAbstract
Abnormal neurites, neuropil threads, are a widespread and characteristic lesion of Alzheimer's disease likely to play a major role in the cognitive impairment of this disease. Contrary to normal neurites, neuropil threads contain straight and paired helical filaments that contain the microtubule-associated protein tau and ubiquitin. It is not known whether these abnormal filaments are added to or replace the normal cytoskeleton. In this study, we examined the fine structure of neuropil threads and carried out a morphometric analysis of the neurofilaments and abnormal filaments contained in the neuropil threads by using an antiserum to tau and colloidal gold immuno- electron microscopy. Almost 70% of the neuropil threads contained straight or paired helical filaments with no neurofilaments. The total number of filaments in each neuropil thread remained essentially unchanged either when straight or paired helical filaments were present alone or when they coexisted either together or with neurofilaments. When the three types of filaments were expressed as a proportion of the total, a linear inverse correlation was found between neurofilaments and straight filaments as well as between straight and paired helical filaments. Approximately 10% of the neuropil threads were found to be myelinated axons. It is concluded that straight filaments are likely to replace neurofilaments, that they in turn might be replaced by paired helical filaments, and that this process occurs in axons as well as dendrites.
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Neuropil threads may represent the majority of tau burden in Alzheimer's disease, and they are thought to originate from neurons containing neurofibrillary tangles.
“Neuropil threads may represent the majority of tau burden in AD, and they are thought to originate from neurons containing NFTs [62–64].”
From The neuropathological diagnosis of Alzheimer's disease (2019) · cites this paper as [63]
Cites
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The neuropathological diagnosis of Alzheimer's disease
DeTure, M. A., & Dickson, D. W. (2019) · Molecular Neurodegeneration · doi:10.1186/s13024-019-0333-5 · Cited by 3,329 · see citing works
Oxidative Damage Is the Earliest Event in Alzheimer Disease
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Self-citationMitochondrial abnormalities in Alzheimer's disease
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Quinone reductase (NQO1), a sensitive redox indicator, is increased in Alzheimer’s disease
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- Authors
- Perry, G., Kawai, M., Tabaton, M., Onorato, M., Mulvihill, P., Richey, P., Morandi, A., Connolly, J., & Gambetti, P.
- Affiliations
- Case Western Reserve University (US)
- ORCID
- Perry, G
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1991-06-01
- Volume
- 11
- Issue
- 6
- Pages
- 1748-1755
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6575401
- OpenAlex
- W2106658584
- Cited by
- 140
- References
- 1
- Citations by year
- 2026: 1 · 2024: 1 · 2022: 1 · 2021: 4 · 2020: 3 · 2019: 6 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 3 · 2012: 2
- FWCI
- 8.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutial Research Information System (University of Genoa) (submittedVersion)
- Funders
- Britton Fund
- National Institutes of Health (5r37ag008155-10, 5r01ag007552-06, 5r01ag009287-08, AG07552, K04-AG00415)
- National Institute on Aging (AG-08155, AG07552, AG009287)
- Fogarty International Center
- 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, neuropil threads, straight filaments, paired helical filaments, neurofilaments, tau protein, ubiquitin, cytoskeleton, myelinated axons, neurofibrillary tangles
- MeSH terms
- Aged, Alzheimer Disease, Axons, Cerebral Cortex, Cytoskeleton, Hippocampus, Humans, Intermediate Filaments, Microtubule-Associated Proteins, Middle Aged, Nerve Tissue Proteins, Reference Values, Microscopy, Immunoelectron, tau Proteins
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