TY - JOUR
T1 - Differential assembly of coexpressed glutamate receptor subunits in neurons of rat cerebral cortex
AU - Brose, Nils
AU - Huntley, George W.
AU - Stern-Bach, Yael
AU - Sharma, Geeta
AU - Morrison, John H.
AU - Heinemann, Stephen F.
PY - 1994/6/17
Y1 - 1994/6/17
N2 - In the rat, subunits of the glutamate receptor family fall into three pharmacologically distinct groups: α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid preferring receptors (Glu R1-4), kainate preferring receptors (Glu R5-7, KA 1, KA 2), and N-methyl-D-aspartate preferring receptors (NMDA R1, NMDA R2A-2D). In the present study, we demonstrate immunocytochemically that the majority of neurons in rat cerebral cortex coexpress members of all three groups of glutamate receptor subunits, Glu R2/3, Glu R5/6/7, and NMDA R1. Using immunoaffinity purified or immunoprecipitated α-amino-3-hydroxy- 5-methyl-4-isoxazole propionic acid, kainate and N-methyl-D-aspartate receptors, we show that α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors containing Glu R1-4, kainate receptors containing Glu R6, Glu R7, and KA 2 and N-methyl-D-aspartate receptors containing NMDA R1 each form distinct protein complexes that do not share subunits. Our data indicate that a mechanism exists which allows for the specific assembly of selected glutamate receptor subunits into functionally and structurally distinct heteromeric receptors.
AB - In the rat, subunits of the glutamate receptor family fall into three pharmacologically distinct groups: α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid preferring receptors (Glu R1-4), kainate preferring receptors (Glu R5-7, KA 1, KA 2), and N-methyl-D-aspartate preferring receptors (NMDA R1, NMDA R2A-2D). In the present study, we demonstrate immunocytochemically that the majority of neurons in rat cerebral cortex coexpress members of all three groups of glutamate receptor subunits, Glu R2/3, Glu R5/6/7, and NMDA R1. Using immunoaffinity purified or immunoprecipitated α-amino-3-hydroxy- 5-methyl-4-isoxazole propionic acid, kainate and N-methyl-D-aspartate receptors, we show that α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors containing Glu R1-4, kainate receptors containing Glu R6, Glu R7, and KA 2 and N-methyl-D-aspartate receptors containing NMDA R1 each form distinct protein complexes that do not share subunits. Our data indicate that a mechanism exists which allows for the specific assembly of selected glutamate receptor subunits into functionally and structurally distinct heteromeric receptors.
UR - http://www.scopus.com/inward/record.url?scp=0028341877&partnerID=8YFLogxK
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C2 - 8207001
AN - SCOPUS:0028341877
SN - 0021-9258
VL - 269
SP - 16780
EP - 16784
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 24
ER -