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Increased expression of NR2A subunit does not alter NMDA‐evoked responses in cultured fetal trisomy 16 mouse hippocampal neurons
Author(s) -
Klein Rebecca C.,
Siarey Richard J.,
Caruso Alessandra,
Rapoport Stanley I.,
Castellino Francis J.,
Galdzicki Zygmunt
Publication year - 2001
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2001.00170.x
Subject(s) - nmda receptor , ifenprodil , hippocampal formation , spermine , biology , glutamate receptor , microbiology and biotechnology , neuroscience , receptor , biochemistry , enzyme
The trisomy 16 (Ts16) mouse is an animal model for human trisomy 21 (Down's syndrome). The gene encoding the NR2A subunit of the NMDA receptor has been localized to mouse chromosome 16. In the present study, western blot analysis revealed a 2.5‐fold increase of NR2A expression in cultured Ts16 embryonic hippocampal neurons. However, this increase did not affect the properties of NMDA‐evoked currents in response to various modulators. The sensitivity of NMDA receptors to transient applications of NMDA, spermine, and Zn 2+ was investigated in murine Ts16 and control diploid cultured embryonic hippocampal neurons. Peak and steady‐state currents evoked by NMDA were potentiated by spermine at concentrations < 1 m m , and inhibited by Zn 2+ in a dose‐dependent and voltage‐independent manner. No marked difference was observed between Ts16 and control diploid neurons for any of these modulators with regard to IC 50 and EC 50 values or voltage dependency. Additionally, inhibition by the NR2B selective inhibitor, ifenprodil, was similar. These results demonstrate that NMDA‐evoked currents are not altered in cultured embryonic Ts16 neurons and suggest that Ts16 neurons contain similar functional properties of NMDA receptors as diploid control neurons despite an increased level of NR2A expression.