Immunohistochemical localization of N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor subunits in the substantianigra pars compacta of the rat
Ds. Albers et al., Immunohistochemical localization of N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor subunits in the substantianigra pars compacta of the rat, NEUROSCIENC, 89(1), 1999, pp. 209-220
Ionotropic glutamate receptors in the substantia nigra pars compacta regula
te the activity of dopamine neurons. We have used dual-label immunofluorese
nce and confocal laser microscopy to study the localization of subunits of
two types of ionotropic receptors within the substantia nigra pars compacta
of the rat. Immunostaining for N-methyl-D-aspartate receptor 1 and glutama
te receptor 2/3 was prominent in the soma and proximal dendrites of all tyr
osine hydroxylase-immunopositive cells, while only low amounts of N-methyl-
D-aspartate receptor 2A and N-methyl-D-aspartate receptor 2B were present.
Selective antibodies were used to determine the isoforms of N-methyl-D-aspa
rtate receptor 1 present. Immunostaining for the N1, C1 and C2 variably spl
iced segments of N-methyl-D-aspartate receptor 1 were scarce in the substan
tia nigra pars compacta, while immunoreactivity for the alternative C2' ter
minus of N-methyl-D-aspartate receptor 1 was quite abundant. Staining for g
lutamate receptor 1 was heterogeneous; about half of the tyrosine hydroxyla
se immunopositive cells stained intensely, while the other half were immuno
negative. The glutamate receptor 1-stained cells were concentrated in the v
entral tier of the substantia nigra pars compacta. Glutamate receptor 4 was
nor found in tyrosine hydroxylase-immunopositive cells within the substant
ia nigra pars compacta.
Together, these data demonstrate that dopaminergic neurons in the substanti
a nigra pars compacta express primarily glutamate receptor 1, glutamate rec
eptor 2/3 and,N-methyl-D-aspartate receptor 1 isoforms containing the alter
native C2' terminus. (C) 1998 IBRO. Published by Elsevier Science Ltd.