» Articles » PMID: 18562611

GluR6/KA2 Kainate Receptors Mediate Slow-deactivating Currents

Overview
Journal J Neurosci
Specialty Neurology
Date 2008 Jun 20
PMID 18562611
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Kainate receptors (KARs) are ionotropic glutamate receptors contributing to EPSCs with a slow-decaying component that is likely essential for synaptic integration. The slow kinetics of KAR-EPSCs markedly contrasts with the fast kinetics reported for recombinant KARs expressed in heterologous systems, for reasons that remain unexplained. Here we have studied the properties of recombinant heteromeric GluR6/KA2 receptors, which compose synaptic KARs. We report that, in response to brief glutamate applications, currents mediated by recombinant GluR6/KA2 receptors, but not GluR6 receptors, decay with a time course similar to KAR-EPSCs. Model simulations suggest that, after brief agonist exposures, GluR6/KA2 currents undergo slow deactivation caused by the stabilization of partially bound open states. We propose, therefore, that the GluR6/KA2 gating features could contribute to the slow KAR-EPSC decay kinetics.

Citing Articles

Trapping of spermine, Kukoamine A, and polyamine toxin blockers in GluK2 kainate receptor channels.

Gangwar S, Yelshanskaya M, Aktolun M, Yen L, Newton T, Stromgaard K Nat Commun. 2024; 15(1):10257.

PMID: 39592599 PMC: 11599716. DOI: 10.1038/s41467-024-54538-x.


Kainate receptor channel opening and gating mechanism.

Gangwar S, Yelshanskaya M, Nadezhdin K, Yen L, Newton T, Aktolun M Nature. 2024; 630(8017):762-768.

PMID: 38778115 PMC: 11186766. DOI: 10.1038/s41586-024-07475-0.


Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels.

Hansen K, Wollmuth L, Bowie D, Furukawa H, Menniti F, Sobolevsky A Pharmacol Rev. 2021; 73(4):298-487.

PMID: 34753794 PMC: 8626789. DOI: 10.1124/pharmrev.120.000131.


Architecture and structural dynamics of the heteromeric GluK2/K5 kainate receptor.

Khanra N, Brown P, Perozzo A, Bowie D, Meyerson J Elife. 2021; 10.

PMID: 33724189 PMC: 7997659. DOI: 10.7554/eLife.66097.


Subunit-selective iGluR antagonists can potentiate heteromeric receptor responses by blocking desensitization.

Pollok S, Reiner A Proc Natl Acad Sci U S A. 2020; 117(41):25851-25858.

PMID: 32999066 PMC: 7568280. DOI: 10.1073/pnas.2007471117.


References
1.
Castillo P, Malenka R, Nicoll R . Kainate receptors mediate a slow postsynaptic current in hippocampal CA3 neurons. Nature. 1997; 388(6638):182-6. DOI: 10.1038/40645. View

2.
Mulle C, Sailer A, Perez-Otano I, Castillo P, Bureau I, Maron C . Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice. Nature. 1998; 392(6676):601-5. DOI: 10.1038/33408. View

3.
Clements J, Lester R, Tong G, Jahr C, Westbrook G . The time course of glutamate in the synaptic cleft. Science. 1992; 258(5087):1498-501. DOI: 10.1126/science.1359647. View

4.
Pinheiro P, Mulle C . Kainate receptors. Cell Tissue Res. 2006; 326(2):457-82. DOI: 10.1007/s00441-006-0265-6. View

5.
Nasu-Nishimura Y, Hurtado D, Braud S, Tang T, Isaac J, Roche K . Identification of an endoplasmic reticulum-retention motif in an intracellular loop of the kainate receptor subunit KA2. J Neurosci. 2006; 26(26):7014-21. PMC: 6673909. DOI: 10.1523/JNEUROSCI.0573-06.2006. View