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

被引:57
作者
Mahadevan, Vivek [1 ]
Pressey, Jessica C. [1 ]
Acton, Brooke A. [1 ]
Uvarov, Pavel [5 ]
Huang, Michelle Y. [1 ]
Chevrier, Jonah [1 ]
Puchalski, Andrew [1 ]
Li, Caiwei M. [1 ]
Ivakine, Evgueni A. [2 ]
Airaksinen, Matti S. [5 ]
Delpire, Eric [3 ]
McInnes, Roderick R. [2 ,4 ]
Woodin, Melanie A. [1 ]
机构
[1] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON M5S 3G5, Canada
[2] Hosp Sick Children, Res Inst, Toronto, ON M5G 1X8, Canada
[3] Vanderbilt Univ, Sch Med, Dept Anesthesiol, Nashville, TN 37232 USA
[4] McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Montreal, PQ H3T 1E2, Canada
[5] Univ Helsinki, Inst Biomed Anat, FIN-00014 Helsinki, Finland
来源
CELL REPORTS | 2014年 / 7卷 / 06期
基金
芬兰科学院; 加拿大健康研究院;
关键词
ACTIVITY-DEPENDENT REGULATION; CL COTRANSPORTER KCC2; SYNAPSES; SUBUNIT; INHIBITION;
D O I
10.1016/j.celrep.2014.05.022
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1762 / 1770
页数:9
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