DEVELOPMENTAL EXPRESSION OF NMDA RECEPTOR SUBUNITS AND THE EMERGENCE OF GLUTAMATE NEUROTOXICITY IN PRIMARY CULTURES OF MURINE CEREBRAL CORTICAL-NEURONS
I. Mizuta et al., DEVELOPMENTAL EXPRESSION OF NMDA RECEPTOR SUBUNITS AND THE EMERGENCE OF GLUTAMATE NEUROTOXICITY IN PRIMARY CULTURES OF MURINE CEREBRAL CORTICAL-NEURONS, Cellular and molecular life sciences, 54(7), 1998, pp. 721-725
Using primary cultures of murine cerebral cortices, we investigated th
e developmental expression of N-methyl-D-aspartate (NMDA) receptor sub
units in relation to the appearance of NMDA receptor-mediated glutamat
e neurotoxicity. The cultures were not affected by glutamate exposure
on culture days 7-9, but became sensitive to glutamate neurotoxicity o
n day II. The expression of NMDA receptor subunit messenger RNAs (mRNA
s) was investigated by means of reverse transcription polymerase chain
reaction (RT-PCR). The epsilon 3-NR2C and epsilon 4-NR2D transcripts
could not be detected in the culture. The epsilon 2-NR2B and zeta 1-NR
1 subunit mRNAs, on the other hand, could be detected clearly and cont
inuously from the culture initiation, and the epsilon 1-NR2A subunit m
RNA became clearly detectable on culture day 4. The expression of thes
e three subunits' proteins in the glutamate-insensitive stage (culture
day 8) and the sensitive stage (day 11) were studied by means of West
ern blotting. The epsilon 2-NR2B and zeta 1-NR1 subunit proteins were
clearly expressed on culture days 8 and 11, but the epsilon 1-NR2A sub
unit protein could hardly be detected on either day 8 or day 11. These
results suggest that the glutamate neurotoxicity in the primary cultu
re was mediated mainly by epsilon 2/zeta 1 NMDA receptors. The time la
g between the protein expression of the epsilon 2-NR2B and zeta 1-NR1
subunits and the emergence of glutamate neurotoxicity may be necessary
for the maturation of functional NMDA receptor systems, including het
eromeric receptor formation, increase in receptor density and maturati
on of the postreceptor signal transduction system.