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CLC-3 chloride channels moderate long-term potentiation at Schaffer collateral-CA1 synapses.

The Journal of physiology | 2013

The chloride channel CLC-3 is expressed in the brain on synaptic vesicles and postsynaptic membranes. Although CLC-3 is broadly expressed throughout the brain, the CLC-3 knockout mouse shows complete, selective postnatal neurodegeneration of the hippocampus, suggesting a crucial role for the channel in maintaining normal brain function. CLC-3 channels are functionally linked to NMDA receptors in the hippocampus; NMDA receptor-dependent Ca(2+) entry, activation of Ca(2+)/calmodulin kinase II and subsequent gating of CLC-3 link the channels via a Ca(2+)-mediated feedback loop. We demonstrate that loss of CLC-3 at mature synapses increases long-term potentiation from 135 ± 4% in the wild-type slice preparation to 154 ± 7% above baseline (P < 0.001) in the knockout; therefore, the contribution of CLC-3 is to reduce synaptic potentiation by ∼40%. Using a decoy peptide representing the Ca(2+)/calmodulin kinase II phosphorylation site on CLC-3, we show that phosphorylation of CLC-3 is required for its regulatory function in long-term potentiation. CLC-3 is also expressed on synaptic vesicles; however, our data suggest functionally separable pre- and postsynaptic roles. Thus, CLC-3 confers Cl(-) sensitivity to excitatory synapses, controls the magnitude of long-term potentiation and may provide a protective limit on Ca(2+) influx.

Pubmed ID: 23165767 RIS Download

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: F31 NS076226
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM07839-30
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM036823
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK080364
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM36823
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007839

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