Cited by 148Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchAdvanced MRI Techniques and Applications

In Vivo Magnetic Resonance Microimaging of Individual Amyloid Plaques in Alzheimer's Transgenic Mice

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Jack, Clifford R., Wengenack, Thomas M., Reyes, Denise A., Garwood, Michael, Curran, Geoffrey L., Borowski, Bret J., Lin, Joseph, Preboske, Gregory M. +3 more·2005·The Journal of Neuroscience

Abstract

The ability to detect individual Alzheimer's amyloid plaques in vivo by magnetic resonance microimaging (MRI) should improve diagnosis and also accelerate discovery of effective therapeutic agents for Alzheimer's disease (AD). Here, we perform in vivo and ex vivo MRI on double transgenic AD mice as well as wild-type mice at varying ages and correlate these with thioflavin-S and iron staining histology. Quantitative counts of individual plaques on MRI increase with age and correlate with histologically determined plaque burden. Plaques 20 microm in diameter can be detected in AD mice as young as 3 months of age with ex vivo MRI. Plaques 35 microm in diameter can be detected by 9 months of age with in vivo MRI. In vivo MRI of individual Alzheimer's amyloid plaques provides a noninvasive estimate of plaque burden in transgenic AD mice that might be useful in assessing the efficacy of amyloid reduction therapies.

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Crossref · 10.1523/jneurosci.2588-05.2005

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  • Aβ plaques could also be detected in mouse AD models using a high-resolution T2-weighted spin-echo sequence.

    “The Aβ plaques could also be detected in mouse AD models using a high-resolution T2-weighted spin-echo sequence (Jack et al., 2005).”
  • MRI scans of post-mortem human brains and a mouse model of Alzheimer's disease show decreases in hippocampal T2* MRI, which is sensitive to the magnetic properties of iron or its spatial variance, attributed in part to iron in Aβ plaques.

    “MRI scans of post-mortem human brains and a mouse model of Alzheimer’s disease show decreases in hippocampal T2* MRI, which is sensitive to the magnetic properties of iron86,87 or its spatial variance, attributed in part to iron in Aβ plaques.88–90”

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References 28 · Cited by 148

Authors
Jack, C. R., Wengenack, T. M., Reyes, D. A., Garwood, M., Curran, G. L., Borowski, B. J., Lin, J., Preboske, G. M., Holasek, S. S., Adriany, G., & Poduslo, J. F.
Affiliations
  • Mayo Clinic (US)
  • University of Minnesota (US)
Venue
The Journal of Neuroscience
Published
2005-10-26
Volume
25
Issue
43
Pages
10041-10048
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2102489568
Cited by
148
References
28
Citations by year
2026: 2 · 2025: 1 · 2024: 1 · 2022: 2 · 2021: 4 · 2020: 2 · 2019: 2 · 2018: 8 · 2017: 5 · 2016: 8 · 2015: 5 · 2014: 7 · 2013: 10 · 2012: 9
FWCI
7.62
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • W. M. Keck Foundation
  • National Institutes of Health (RR08079)
  • National Institute on Aging (AG22034, R01AG022034)
  • National Center for Research Resources (RR 08079, P41RR008079)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
Keywords
Alzheimer's disease, amyloid plaques, transgenic mice, plaque detection, plaque burden, thioflavin S staining, iron staining, non-invasive imaging, ex vivo MRI
MeSH terms
Age Factors, Alzheimer Disease, Animals, Brain Mapping, Disease Models, Animal, Magnetic Resonance Imaging, Mice, Transgenic, Staining and Labeling, Thiazoles, Mice, Benzothiazoles, Plaque, Amyloid

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