Neuron
Volume 82, Issue 4, 21 May 2014, Pages 848-858
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Article
Cornichon2 Dictates the Time Course of Excitatory Transmission at Individual Hippocampal Synapses

https://doi.org/10.1016/j.neuron.2014.03.031Get rights and content
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Highlights

  • CNIH2 dictates slow EPSC decay in MFB-mossy cell synapses in the hippocampus

  • CNIH2 determines channel gating of postsynaptic AMPARs

  • Knockdown of CNIH2 leads to fast EPSCs typical for MFB-interneuron synapses

  • CNIH2 is the molecular distinction between slow and fast EPSC phenotype

Summary

Cornichon2 (CNIH2), an integral component of AMPA receptor (AMPAR) complexes in the mammalian brain, slows deactivation and desensitization of heterologously reconstituted receptor channels. Its significance in neuronal signal transduction, however, has remained elusive. Here we show by paired recordings that CNIH2-containing AMPARs dictate the slow decay of excitatory postsynaptic currents (EPSCs) elicited in hilar mossy cells of the hippocampus by single action potentials in mossy fiber boutons (MFB). Selective knockdown of CNIH2 markedly accelerated EPSCs in individual MFB-mossy cell synapses without altering the EPSC amplitude. In contrast, the rapidly decaying EPSCs in synapses between MFBs and aspiny interneurons that lack expression of CNIH2 were unaffected by the protein knockdown but were slowed by virus-directed expression of CNIH2. These results identify CNIH2 as the molecular distinction between slow and fast EPSC phenotypes and show that CNIH2 influences the time course and, hence, the efficacy of excitatory synaptic transmission.

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