EXPRESSION OF NMDAR2D GLUTAMATE-RECEPTOR SUBUNIT MESSENGER-RNA IN NEUROCHEMICALLY IDENTIFIED INTERNEURONS IN THE RAT NEOSTRIATUM, NEOCORTEXAND HIPPOCAMPUS
Dg. Standaert et al., EXPRESSION OF NMDAR2D GLUTAMATE-RECEPTOR SUBUNIT MESSENGER-RNA IN NEUROCHEMICALLY IDENTIFIED INTERNEURONS IN THE RAT NEOSTRIATUM, NEOCORTEXAND HIPPOCAMPUS, Molecular brain research, 42(1), 1996, pp. 89-102
NMDA receptors are composed of proteins from two families: NMDAR1, whi
ch are required for channel activity, and NMDAR2, which modulate prope
rties of the channels. The mRNA encoding the NMDAR2D subunit has a hig
hly restricted pattern of expression: in the forebrain, it is found in
only a small subset of cortical, neostriatal and hippocampal neurons.
We have used a quantitative double-label in situ hybridization method
to examine the expression of NMDAR2D mRNA in neurochemically defined
populations of neurons. In the neostriatum, NMDAR2D was expressed by t
he interneuron populations marked by preprosomatostatin (SOM), the 67-
kDa form of glutamic acid decarboxylase (GAD(67)), parvalbumin (PARV),
and choline acetyltransferase (ChAT) mRNAs but not by the projection
neurons expressing beta-preprotachykinin (SP) or preproenkephalin (ENK
) mRNAs. In the neocortex, NMDAR2D expression was observed in only a s
mall number of neurons, but these included almost all of the SOM-, GAD
(67)- and PARV-expressing interneurons. In the hippocampus, NMDAR2D wa
s not present in pyramidal or granule cells, but was abundant in SOM-,
GAD(67)-, and PARV-positive interneurons. NMDAR2D expression appears
to be a property shared by interneurons in several regions of the brai
n. The unique electrophysiological characteristics conveyed by this su
bunit, which include resistance to blockade by magnesium ion and long
channel offset latencies, may be important for the integrative functio
ns of these neurons. NMDAR2D-containing receptor complexes may prove t
o be important therapeutic targets in human disorders of movement. In
addition, the presence of NMDAR2D subunits may contribute to the diffe
rential vulnerability of interneurons to excitotoxic injury.