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The Journal of Neuroscience, January 15, 2000, 20(2):660-665
Restricted Expression of G86R Cu/Zn Superoxide Dismutase in
Astrocytes Results in Astrocytosis But Does Not Cause Motoneuron
Degeneration
Yun H.
Gong1,
Alexander
S.
Parsadanian2,
Albina
Andreeva1,
William D.
Snider3, and
Jeffrey L.
Elliott1
1 Department of Neurology, University of Texas,
Southwestern Medical Center, Dallas, Texas 75235, 2 Department of Neurology, Washington University School of
Medicine, St. Louis, Missouri 63110, and 3 University of
North Carolina Neuroscience Center, School of Medicine, University of
North Carolina, Chapel Hill, North Carolina 27599
Evidence garnered from both human autopsy studies and genetic
animal models has suggested a potential role for astrocytes in the
pathogenesis of amyotrophic lateral sclerosis (ALS). Currently, mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1) represent the only known cause of motoneuron loss in the disease, producing 21q linked familial ALS (FALS). To determine whether astrocytic dysfunction has a primary role in familial ALS, we have
generated multiple lines of transgenic mice expressing G86R mutant SOD1
restricted to astrocytes. In GFAP-m SOD1 mice, astrocytes exhibit
significant hypertrophy and increased GFAP reactivity as the animals
mature. However, GFAP-mutant SOD1 transgenic mice develop normally and
do not experience spontaneous motor deficits with increasing age.
Histological examination of spinal cord in aged GFAP-mSOD1 mice reveals
normal motoneuron and microglial morphology. These results indicate
that 21q linked FALS is not a primary disorder of astrocytes, and that
expression of mutant SOD1 restricted to astrocytes is not sufficient to
cause motoneuron degeneration in vivo. Expression of
mutant SOD1 in other cell types, most likely neurons, is critical for
the initiation of disease.
Key words:
amyotrophic lateral sclerosis; glutamate; mouse; transgenic; glia; gliosis
Copyright © 2000 Society for Neuroscience 0270-6474/00/202660-06$05.00/0
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