Em. Mineff et al., Immunocytochemical localization of the AMPA receptor subunits in the mesencephalic trigeminal nucleus of the rat, ARCH PHYS B, 106(3), 1998, pp. 203-209
The mesencephalic trigeminal nucleus is composed of large (35-50 mu m) pseu
do-unipolar neurons. Closely associated with them are small (< 20 mu m) mul
tipolar neurons. An unique peculiarity of the pseudo-unipolar perikarya is
that they receive synaptic input from various sources, which sets them apar
t from the dorsal root and cranial nerves sensory ganglia neurons. Whereas
glutamate is the best neurotransmitter candidate in pseudo-unipolar neurons
, glutamatergic input into them has not yet been reported. AMPA glutamate r
eceptors are implicated in fast excitatory glutamatergic synaptic transmiss
ion. They have been localized ultrastructurally at postsynaptic sites. This
study demonstrates that the pseudo-unipolar neurons of the mesencephalic t
rigeminal nucleus express AMPA glutamate receptor subunits, which indicates
that these neurons receive glutamatergic input. Serial sections from the r
ostral pens and midbrain of Sprague-Dawley rats were immunostained with ant
ibodies against C-terminus of AMPA receptor subunits: GluR1, GluR2/3, and G
luR4. The immunoreaction was visualized with avidin-biotin-peroxidase/DAB f
or light and electron microscopy. With GluR1 antibody only the smallest mul
tipolar neurons were recognized as immunopositive within the mesencephalic
trigeminal nucleus. GluR2/3 stained the pseudo-unipolar neurons intensely w
ithin the entire rostro-caudal extent of the nucleus. In addition the forme
r antibody stained small multipolar neurons within the mesencephalic trigem
inal nucleus, though with somewhat larger dimensions than those immunoreact
ive for GluR1. Whereas the overall staining with GluR4 antibody was scant,
those pseudo-unipolar neurons that were stained, were strongly stained. Fur
thermore, a considerable number of microglial cells within and surrounding
the mesencephalic trigeminal nucleus displayed very intense immunoreactivit
y for GluR4. These results are discussed in the light of the glutamate rece
ptor subunit composition.