Premium
Pre‐synaptic glycine GlyT1 transporter – NMDA receptor interaction: relevance to NMDA autoreceptor activation in the presence of Mg 2+ ions
Author(s) -
Musante Veronica,
Summa Maria,
Cunha Rodrigo A.,
Raiteri Maurizio,
Pittaluga Anna
Publication year - 2011
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 - 10.1111/j.1471-4159.2011.07223.x
Subject(s) - nmda receptor , glycine , chemistry , glutamatergic , autoreceptor , glutamate receptor , kynurenic acid , agonist , dizocilpine , glycine receptor , sarcosine , biophysics , biochemistry , amino acid , biology , receptor
J. Neurochem. (2011) 117 , 516–527. Abstract Rat hippocampal glutamatergic terminals possess NMDA autoreceptors whose activation by low micromolar NMDA elicits glutamate exocytosis in the presence of physiological Mg 2+ (1.2 mM), the release of glutamate being significantly reduced when compared to that in Mg 2+ ‐free condition. Both glutamate and glycine were required to evoke glutamate exocytosis in 1.2 mM Mg 2+ , while dizocilpine, cis ‐4‐[phosphomethyl]‐piperidine‐2‐carboxylic acid and 7‐Cl‐kynurenic acid prevented it, indicating that occupation of both agonist sites is needed for receptor activation. d ‐serine mimicked glycine but also inhibited the NMDA/glycine‐induced release of [ 3 H] d ‐aspartate, thus behaving as a partial agonist. The NMDA/glycine‐induced release in 1.2 mM Mg 2+ strictly depended on glycine uptake through the glycine transporter type 1 (GlyT1), because the GlyT1 blocker N ‐[3‐(4′‐fluorophenyl)‐3‐(4′‐phenylphenoxy)propyl])sarcosine hydrochloride, but not the GlyT2 blocker Org 25534, prevented it. Accordingly, [ 3 H]glycine was taken up during superfusion, while lowering the external concentration of Na + , the monovalent cation co‐transported with glycine by GlyT1, abrogated the NMDA‐induced effect. Western blot analysis of subsynaptic fractions confirms that GlyT1 and NMDA autoreceptors co‐localize at the pre‐synaptic level, where GluN3A subunits immunoreactivity was also recovered. It is proposed that GlyT1s coexist with NMDA autoreceptors on rat hippocampal glutamatergic terminals and that glycine taken up by GlyT1 may permit physiological activation of NMDA pre‐synaptic autoreceptors.