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Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons

KCC2 is the neuron-specific K+-Cl(−) cotransporter required for maintaining low intracellular Cl(−), which is essential for fast inhibitory synaptic transmission in the mature CNS. Despite the requirement of KCC2 for inhibitory synaptic transmission, understanding of the cellular mechanisms that reg...

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Autores principales: Mahadevan, Vivek, Pressey, Jessica C., Acton, Brooke A., Uvarov, Pavel, Huang, Michelle Y., Chevrier, Jonah, Puchalski, Andrew, Li, Caiwei M., Ivakine, Evgueni A., Airaksinen, Matti S., Delpire, Eric, McInnes, Roderick R., Woodin, Melanie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340141/
https://www.ncbi.nlm.nih.gov/pubmed/24910435
http://dx.doi.org/10.1016/j.celrep.2014.05.022
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author Mahadevan, Vivek
Pressey, Jessica C.
Acton, Brooke A.
Uvarov, Pavel
Huang, Michelle Y.
Chevrier, Jonah
Puchalski, Andrew
Li, Caiwei M.
Ivakine, Evgueni A.
Airaksinen, Matti S.
Delpire, Eric
McInnes, Roderick R.
Woodin, Melanie A.
author_facet Mahadevan, Vivek
Pressey, Jessica C.
Acton, Brooke A.
Uvarov, Pavel
Huang, Michelle Y.
Chevrier, Jonah
Puchalski, Andrew
Li, Caiwei M.
Ivakine, Evgueni A.
Airaksinen, Matti S.
Delpire, Eric
McInnes, Roderick R.
Woodin, Melanie A.
author_sort Mahadevan, Vivek
collection PubMed
description KCC2 is the neuron-specific K+-Cl(−) cotransporter required for maintaining low intracellular Cl(−), which is essential for fast inhibitory synaptic transmission in the mature CNS. Despite the requirement of KCC2 for inhibitory synaptic transmission, understanding of the cellular mechanisms that regulate KCC2 expression and function is rudimentary. We examined KCC2 in its native protein complex in vivo to identify key KCC2-interacting partners that regulate KCC2 function. Using blue native-polyacrylamide gel electrophoresis (BN-PAGE), we determined that native KCC2 exists in a macromolecular complex with kainate-type glutamate receptors (KARs). We found that KAR subunits are required for KCC2 oligomerization and surface expression. In accordance with this finding, acute and chronic genetic deletion of KARs decreased KCC2 function and weakened synaptic inhibition in hippocampal neurons. Our results reveal KARs as regulators of KCC2, significantly advancing our growing understanding of the tight interplay between excitation and inhibition.
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spelling pubmed-63401412019-01-21 Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons Mahadevan, Vivek Pressey, Jessica C. Acton, Brooke A. Uvarov, Pavel Huang, Michelle Y. Chevrier, Jonah Puchalski, Andrew Li, Caiwei M. Ivakine, Evgueni A. Airaksinen, Matti S. Delpire, Eric McInnes, Roderick R. Woodin, Melanie A. Cell Rep Article KCC2 is the neuron-specific K+-Cl(−) cotransporter required for maintaining low intracellular Cl(−), which is essential for fast inhibitory synaptic transmission in the mature CNS. Despite the requirement of KCC2 for inhibitory synaptic transmission, understanding of the cellular mechanisms that regulate KCC2 expression and function is rudimentary. We examined KCC2 in its native protein complex in vivo to identify key KCC2-interacting partners that regulate KCC2 function. Using blue native-polyacrylamide gel electrophoresis (BN-PAGE), we determined that native KCC2 exists in a macromolecular complex with kainate-type glutamate receptors (KARs). We found that KAR subunits are required for KCC2 oligomerization and surface expression. In accordance with this finding, acute and chronic genetic deletion of KARs decreased KCC2 function and weakened synaptic inhibition in hippocampal neurons. Our results reveal KARs as regulators of KCC2, significantly advancing our growing understanding of the tight interplay between excitation and inhibition. 2014-06-05 2014-06-26 /pmc/articles/PMC6340141/ /pubmed/24910435 http://dx.doi.org/10.1016/j.celrep.2014.05.022 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Mahadevan, Vivek
Pressey, Jessica C.
Acton, Brooke A.
Uvarov, Pavel
Huang, Michelle Y.
Chevrier, Jonah
Puchalski, Andrew
Li, Caiwei M.
Ivakine, Evgueni A.
Airaksinen, Matti S.
Delpire, Eric
McInnes, Roderick R.
Woodin, Melanie A.
Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons
title Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons
title_full Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons
title_fullStr Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons
title_full_unstemmed Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons
title_short Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons
title_sort kainate receptors coexist in a functional complex with kcc2 and regulate chloride homeostasis in hippocampal neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340141/
https://www.ncbi.nlm.nih.gov/pubmed/24910435
http://dx.doi.org/10.1016/j.celrep.2014.05.022
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