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Original Research
MRI and histological analysis of beta-amyloid plaques in both human Alzheimer's disease and APP/PS1 transgenic mice
Article first published online: 22 APR 2009
DOI: 10.1002/jmri.21731
Copyright © 2009 Wiley-Liss, Inc.
Additional Information
How to Cite
Meadowcroft, M. D., Connor, J. R., Smith, M. B. and Yang, Q. X. (2009), MRI and histological analysis of beta-amyloid plaques in both human Alzheimer's disease and APP/PS1 transgenic mice. J. Magn. Reson. Imaging, 29: 997–1007. doi: 10.1002/jmri.21731
Publication History
- Issue published online: 22 APR 2009
- Article first published online: 22 APR 2009
- Manuscript Accepted: 9 JAN 2009
- Manuscript Received: 14 OCT 2008
Funded by
- NIH. Grant Numbers: 5R01EB000459-4, R01AG027771
- George M. Leader Foundation
- Pennsylvania Department of Health
- Abstract
- Article
- References
- Cited By
Keywords:
- beta-amyloid (Aβ) plaques;
- MRI microscopy;
- iron;
- APP/PS1 mouse
Abstract
Purpose
To investigate the relationship between MR image contrast associated with beta-amyloid (Aβ) plaques and their histology and compare the histopathological basis of image contrast and the relaxation mechanism associated with Aβ plaques in human Alzheimer's disease (AD) and transgenic APP/PS1 mouse tissues.
Materials and Methods
With the aid of the previously developed histological coil, T
-weighted images and R
parametric maps were directly compared with histology stains acquired from the same set of Alzheimer's and APP/PS1 tissue slices.
Results
The electron microscopy and histology images revealed significant differences in plaque morphology and associated iron concentration between AD and transgenic APP/PS1 mice tissue samples. For AD tissues, T
contrast of Aβ-plaques was directly associated with the gradation of iron concentration. Plaques with significantly less iron load in the APP/PS1 animal tissues are equally conspicuous as the human plaques in the MR images.
Conclusion
These data suggest a duality in the relaxation mechanism where both high focal iron concentration and highly compact fibrillar beta-amyloid masses cause rapid proton transverse magnetization decay. For human tissues, the former mechanism is likely the dominant source of R
relaxation; for APP/PS1 animals, the latter is likely the major cause of increased transverse proton relaxation rate in Aβ plaques. The data presented are essential for understanding the histopathological underpinning of MRI measurement associated with Aβ plaques in humans and animals. J. Magn. Reson. Imaging 2009;29:997–1007. © 2009 Wiley-Liss, Inc.