Cited by 192Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchNeuroinflammation and Neurodegeneration Mechanisms

Tau conformational changes correspond to impairments of episodic memory in mild cognitive impairment and Alzheimer's disease

Ghoshal, N·2002·Experimental Neurology

Abstract

A multitiered strategy was adopted to assess tau conformational changes within fibrillar lesions during the progression of Alzheimer's disease (AD). Anti-tau monoclonal antibodies whose epitopes are distributed across much of the molecule were used to probe vulnerable brain regions in 37 clinically staged cases obtained from the Religious Orders Study. In this way, tau conformational changes were evaluated as the disease progressed from early cognitive decline to AD. These analyses revealed three main findings. First, the presence of granulovacuolar and fibrillar lesions correlates with several measures of episodic memory, suggesting that these lesions significantly contribute to cognitive dysfunction. Second, neuropil threads precede the appearance of neurofibrillary tangles that in turn precede the appearance of neuritic plaques. Third, tau structural changes, or "conformational signatures," emerged as a result of in situ reactivity to a subset of antibodies and nonreactivity to others, thereby reflecting the underlying status of the tau molecule within the fibrillar lesions. These signatures allowed us to document a sequence of tau conformational changes that occur during AD and to correlate these changes with episodic memory deficits. Furthermore, we were able to compare conformational signatures of tau among different lesion types and determine that the molecular profile of tau is lesion-specific.

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Crossref · 10.1006/exnr.2002.8014

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  • Extracellular Aβ can stimulate tau phosphorylation and aggregation in neurons with axons projecting into the injection site in p301L mice, but not wild type mice.

    “extracellular accumulations of Aβ can stimulate tau phosphorylation and aggregation in neurons with axons projecting into the injection site in mice expressing the mutant FTDP-17 (p301L) form of human tau, but not wild type mice19,20,22.”

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Authors
Ghoshal, N.
Affiliations
Northwestern University (US)
Corresponding author
Ghoshal, N
Venue
Experimental Neurology
Publisher
Elsevier BV
Published
2002-10
Volume
177
Issue
2
Pages
475-493
ISSN
0014-4886 (ISSN-L)
OpenAlex
W2079821580
Cited by
192
References
10
Citations by year
2026: 4 · 2025: 4 · 2024: 5 · 2023: 8 · 2022: 8 · 2021: 8 · 2020: 13 · 2019: 13 · 2018: 5 · 2017: 6 · 2016: 10 · 2015: 7 · 2014: 6 · 2013: 9 · 2012: 13
FWCI
4.80
Type
journal article
Language
en
Open access
closed
Locations
  • Experimental Neurology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute on Aging (AG-15819, AG 10161, AG-14449, AG09465, P01AG014449, AG09466, P30AG010161, P01AG009466)
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
tau protein, Alzheimer's disease, mild cognitive impairment, episodic memory, neurofibrillary tangles, neuritic plaques, neuropil threads, Religious Orders Study
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Antibody Specificity, Epitopes, Cognition Disorders, Female, Follow-Up Studies, Hippocampus, Humans, Longitudinal Studies, Male, Memory Disorders, Microscopy, Fluorescence, Neuropsychological Tests, Predictive Value of Tests, Protein Conformation, Protein Kinases, Neurofibrillary Tangles, tau Proteins, Disease Progression, Casein Kinases

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