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Volume 17, Number 2,
Issue of January 15, 1997
pp. 819-833
Copyright ©1997 Society for Neuroscience
Cellular, Subcellular, and Subsynaptic Distribution of AMPA-Type
Glutamate Receptor Subunits in the Neostriatum of the Rat
Received Sept. 4, 1996; revised Oct. 29, 1996; accepted Nov. 4, 1996.
Véronique Bernard,
Peter Somogyi, and
J. Paul Bolam
Medical Research Council, Anatomical Neuropharmacology Unit,
University Department of Pharmacology, Oxford University, Oxford
OX1 3TH, United Kingdom
Glutamate released in the basal ganglia is involved in the
expression of clinical symptoms of neurodegenerative diseases like Parkinson's or Huntington's. Neostriatal neurons are the targets of
glutamatergic inputs derived from the cortex and the thalamus acting
via AMPA-type as well as other glutamate receptors. To determine the
location of subunits of the AMPA subclass of glutamate receptors (GluR)
in the rat neostriatum, we applied multiple immunocytochemical techniques using anti-peptide antibodies against the GluR1, GluR2/3, and GluR4 subunits at both the light and electron microscopic levels.
All medium spiny efferent neurons, some of which were identified as
striatonigral neurons, displayed immunoreactivity for GluR1 and GluR2/3
subunits. Double immunofluorescence revealed that at least 70-90% of
parvalbumin-immunopositive GABAergic interneurons were immunoreactive
for each of GluR1, GluR2/3, or GluR4 subunits and that at least 40% of
choline acetyltransferase-immunopositive cholinergic interneurons were
immunopositive for GluR1 or GluR4 subunits. The majority of nitric
oxide synthase-immunopositive neurons had no detectable
immunoreactivity for any of the AMPA receptor subunits. Electron
microscopic analysis confirmed the presence of immunoreactivity for
GluR1 and GluR2/3 in the perikarya of spiny neurons and interneurons
and GluR4 in perikarya of interneurons only. GluR1 and GluR2/3 subunits
were detected in dendrites and spines. A significant population of
extrasynaptic receptors was revealed by pre-embedding immunogold
labeling along the plasma membranes of perikarya, dendrites, and
spines. Receptors were concentrated in the postsynaptic membrane
specialization of asymmetrical synapses, as revealed by the
postembedding immunogold method. Quantitative analysis demonstrated
that immunoreactivity for the GluR1 and GluR2/3 subunits is higher at
the periphery than at the middle of the postsynaptic membrane
specialization.
Our results demonstrate that AMPA receptor subunits are distributed
widely and heterogeneously among striatal neurons and are concentrated
on the postsynaptic membrane of asymmetrical synaptic specializations,
although extrasynaptic receptors are also present.
Key words:
synaptic junction;
immunohistochemistry;
immunogold;
GluR1;
GluR2/3;
GluR4
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