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Vol. 62, Issue 4, 817-827, October 2002
1 Glycine Receptor Increases with
Receptor Density
Unité Mixte Recherche Centre National de la Recherche
Scientifique 7102, Université Pierre et Marie Curie, Paris,
France (P.L., E.M., C.I.B.); Institut National de la Santé et de
la Recherche Médicale U497, Ecole Normale Supérieure,
Paris, France (J.M., C.V., A.T.)
Variations in the number of receptors at glycinergic synapses are now
established and are believed to contribute to inhibitory synaptic
plasticity. However, the relation between glycine receptor (GlyR)
kinetics and density is still unclear. We used outside-out patch-clamp
recordings and fast-flow application techniques to resolve fast
homomeric GlyR
1 kinetics and to determine how the functional
properties of these receptors depend on their density and on the
presence of the anchoring protein gephyrin. The expression of GlyRs in
human embryonic kidney cells increased with time and was correlated
with an increase in GlyR desensitization at 2 days after transfection.
Cotransfection of homomeric GlyR
1 bearing the gephyrin-binding site
with gephyrin also increased desensitization but at 1 day after
transfection compared with transfections of homomeric GlyR
1 without
gephyrin. This increase results from the occurrence of a fast
desensitization component and short applications of a saturating
concentration of glycine suffice to promote a rapidly entered
desensitized closed state. The level of desensitization changed neither
the EC50 value nor the Hill coefficient of the glycine
dose-response curves because the amplitude of the current was measured
at the peak of the responses. These results demonstrate that variations
in GlyR density during cluster formation result from a change in GlyR
efficiency due to modifications in their desensitization properties.
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