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The Journal of Neuroscience, May 1, 2000, 20(9):3191-3199
Protein Aggregation after Transient Cerebral Ischemia
B. R.
Hu1,
M. E.
Martone2,
Y. Z.
Jones2, and
C. L.
Liu1
1 Laboratory of Neurochemistry, Center for the Study of
Neurological Disease, Queen's Medical Center, Honolulu, Hawaii
96813, and 2 National Center for Microscopy and Imaging
Research at San Diego, University of California, La Jolla, CA
92093-0608
Protein aggregates containing ubiquitinated proteins are commonly
present in neurodegenerative disorders and have been considered to
cause neuronal degeneration. Here, we report that transient cerebral
ischemia caused severe protein aggregation in hippocampal CA1 neurons.
By using ethanolic phosphotungstic acid electron microscopy (EM)
and ubiquitin immunogold EM, we found that protein aggregates were
accumulated in CA1 neurons destined to die 72 hr after 15 min of
cerebral ischemia. Protein aggregates appeared as clumps of
electron-dense materials that stained heavily for ubiquitin and were
associated with various intracellular membranous structures. The
protein aggregates appeared at 4 hr and progressively accumulated at 24 and 48 hr of reperfusion in CA1 dying neurons. However, they were
rarely observed in dentate gyrus neurons that were resistant to
ischemia. At 4 hr of reperfusion, protein aggregates were mainly
associated with intracellular vesicles in the soma and dendrites, and
the nuclear membrane. By 24 hr of reperfusion, the aggregates were also
associated with mitochondria, the Golgi apparatus, and the dendritic
plasmalemma. High-resolution confocal microscopy further demonstrated
that protein aggregates containing ubiquitin were persistently and
progressively accumulated in all CA1 dying neurons but not in neuronal
populations that survive in this model. We conclude that proteins are
severely aggregated in hippocampal neurons vulnerable to transient
brain ischemia. We hypothesize that the accumulation of protein
aggregates cause ischemic neuronal death.
Key words:
brain ischemia; protein aggregation; ubiquitin; neuronal
death; intracellular vesicles; mitochondrion; dendritic membranes; ethanolic phosphotungstic acid; electron microscopy; confocal
microscopy
Copyright © 2000 Society for Neuroscience 0270-6474/00/2093191-09$05.00/0
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