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In Vivo Multiphoton Imaging of a Transgenic Mouse Model of Alzheimer Disease Reveals Marked Thioflavine-S-Associated Alterations in Neurite Trajectories
by
KAJDASZ, S. T.
, MCLELLAN, M. E.
, HYMAN, B. T.
, DʼAMORE, J. D.
, STERN, E. A.
, BACSKAI, B. J.
in
Aging - metabolism
/ Aging - pathology
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer Disease - physiopathology
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Axons - metabolism
/ Axons - pathology
/ Biological and medical sciences
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - pathology
/ Cerebral Cortex - physiopathology
/ Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
/ Dendrites - metabolism
/ Dendrites - pathology
/ Dextrans
/ Disease Models, Animal
/ Fluorescent Dyes
/ Medical sciences
/ Mice
/ Mice, Inbred C57BL
/ Mice, Transgenic
/ Microscopy, Fluorescence, Multiphoton
/ Neurites - metabolism
/ Neurites - pathology
/ Neurology
/ Neuropil - metabolism
/ Neuropil - pathology
/ Plaque, Amyloid - metabolism
/ Plaque, Amyloid - pathology
/ Thiazoles - metabolism
2003
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In Vivo Multiphoton Imaging of a Transgenic Mouse Model of Alzheimer Disease Reveals Marked Thioflavine-S-Associated Alterations in Neurite Trajectories
by
KAJDASZ, S. T.
, MCLELLAN, M. E.
, HYMAN, B. T.
, DʼAMORE, J. D.
, STERN, E. A.
, BACSKAI, B. J.
in
Aging - metabolism
/ Aging - pathology
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer Disease - physiopathology
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Axons - metabolism
/ Axons - pathology
/ Biological and medical sciences
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - pathology
/ Cerebral Cortex - physiopathology
/ Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
/ Dendrites - metabolism
/ Dendrites - pathology
/ Dextrans
/ Disease Models, Animal
/ Fluorescent Dyes
/ Medical sciences
/ Mice
/ Mice, Inbred C57BL
/ Mice, Transgenic
/ Microscopy, Fluorescence, Multiphoton
/ Neurites - metabolism
/ Neurites - pathology
/ Neurology
/ Neuropil - metabolism
/ Neuropil - pathology
/ Plaque, Amyloid - metabolism
/ Plaque, Amyloid - pathology
/ Thiazoles - metabolism
2003
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In Vivo Multiphoton Imaging of a Transgenic Mouse Model of Alzheimer Disease Reveals Marked Thioflavine-S-Associated Alterations in Neurite Trajectories
by
KAJDASZ, S. T.
, MCLELLAN, M. E.
, HYMAN, B. T.
, DʼAMORE, J. D.
, STERN, E. A.
, BACSKAI, B. J.
in
Aging - metabolism
/ Aging - pathology
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer Disease - physiopathology
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Axons - metabolism
/ Axons - pathology
/ Biological and medical sciences
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - pathology
/ Cerebral Cortex - physiopathology
/ Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
/ Dendrites - metabolism
/ Dendrites - pathology
/ Dextrans
/ Disease Models, Animal
/ Fluorescent Dyes
/ Medical sciences
/ Mice
/ Mice, Inbred C57BL
/ Mice, Transgenic
/ Microscopy, Fluorescence, Multiphoton
/ Neurites - metabolism
/ Neurites - pathology
/ Neurology
/ Neuropil - metabolism
/ Neuropil - pathology
/ Plaque, Amyloid - metabolism
/ Plaque, Amyloid - pathology
/ Thiazoles - metabolism
2003
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In Vivo Multiphoton Imaging of a Transgenic Mouse Model of Alzheimer Disease Reveals Marked Thioflavine-S-Associated Alterations in Neurite Trajectories
Journal Article
In Vivo Multiphoton Imaging of a Transgenic Mouse Model of Alzheimer Disease Reveals Marked Thioflavine-S-Associated Alterations in Neurite Trajectories
2003
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Overview
Postmortem analyses of senile plaques reveal numerous dystrophic processes in their vicinity. We used in vivo multiphoton microscopy of a transgenic model of Alzheimer disease (AD) to simultaneously image senile plaques and nearby neuronal processes. Plaques were labeled by immunofluorescent staining or thioflavine-S and neuronal processes were labeled with a fluorescent dextran conjugate. Imaging of 3-dimensional volumes in the vicinity of plaques revealed subtle changes in neurite geometry in or near diffuse plaques. By contrast, disruptions in neurite morphology, including dystrophic neurites immediately surrounding plaques as well as major alterations in neurite trajectories, were seen in association with thioflavine-S-positive plaques. Nearly half of all labeled processes that came within 50 μm of a thioflavine-S-positive plaque were altered, suggesting a fairly large “halo” of neuropil alterations that extend beyond the discrete border of a thioflavine-S plaque. These results support the hypothesis that compact thioflavine-S-positive plaques disrupt the neuropil in AD.
Publisher
American Association of Neuropathologists, Inc,Lippincott Williams & Wilkins,Oxford University Press
Subject
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer Disease - physiopathology
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Biological and medical sciences
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - physiopathology
/ Dextrans
/ Mice
/ Microscopy, Fluorescence, Multiphoton
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