Cellular and subcellular distribution of AMPA-type glutamate receptor subunits and metabotropic glutamate receptor 1 alpha in the cochlear nucleus ofthe horseshoe bat (Rhinolophus rouxi)
M. Kemmer et M. Vater, Cellular and subcellular distribution of AMPA-type glutamate receptor subunits and metabotropic glutamate receptor 1 alpha in the cochlear nucleus ofthe horseshoe bat (Rhinolophus rouxi), HEARING RES, 156(1-2), 2001, pp. 128-142
Ionotropic alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) sel
ective glutamate receptors (GluRs) are the main mediators of fast excitator
y neurotransmission and composed of a variable combination of four differen
t subunits (GluR1-4). The metabotropic glutamate receptor 1 alpha (mGluR1 a
lpha) is involved in plastic synaptic events, Since horseshoe bats strongly
depend on temporal cues for acoustic imaging by echolocation and exhibit p
rominent species specific specializations of the cochlear nucleus (CN), the
subunit distribution of AMPA selective GluRs and the distribution of mGluR
1 alpha was studied at the light and electron microscopic level with preemb
edding immunocytochemistry. Immunoreactivity to GluR1 was low throughout th
e CN. All types of projection neurons of the ventral CN expressed distinct
GluR2/3 and GluR4 immunoreactivity with GluR4-labeling especially prominent
in multipolar and octopus cell-like neurons of the posteroventral CN. The
AMPA and metabotropic receptor inventory of the laminated ventral subdivisi
on of the dorsal CN (DCNv) agreed with that reported in other mammals, wher
eas the specialized dorsal non-laminated subdivision of DCN (DCNd) lacked t
he prominent labeling for GluR2/3 and mGluR1 alpha that characterizes cartw
heel cells of DCNv. Distinct GluR2/3 and GluR4 immunoreactivity combined wi
th low expression of mGluR1 alpha immunoreactivity was characteristic for f
usiform cells of DCNv and DCNd. Tuberculoventral cells of both the deep DCN
v and the DCNd exhibited light to moderate GluR2/3 and GluR4 immunoreactivi
ty. The staining patterns in DCNd thus indicate a loss of cerebellar-like m
icrocircuits and a conservation of frequency specific circuitry of the deep
and fusiform cell layers of the mammalian DCN. (C) 2001 Elsevier Science B
.V. All rights reserved.