期刊
NEURON
卷 37, 期 4, 页码 625-638出版社
CELL PRESS
DOI: 10.1016/S0896-6273(02)01191-1
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资金
- Medical Research Council [G9629038] Funding Source: Medline
- Wellcome Trust [059917] Funding Source: Medline
- MRC [G9629038] Funding Source: UKRI
- Medical Research Council [G9629038] Funding Source: researchfish
We identified four PDZ domain-containing proteins, syntenin, PICK1, GRIP, and PSD95, as interactors with the kainate receptor (KAR) subunits GluR5(2b), GluR5(2c), and GluR6. Of these, we show that both GRIP and PICK1 interactions are required to maintain KAR-mediated synaptic function at mossy fiber-CA3 synapses. In addition, PKCalpha can phosphorylate ct-GluR5(2b) at residues S880 and S886, and PKC activity is required to maintain KAR-mediated synaptic responses. We propose that PICK1 targets PKCalpha to phosphorylate KARs, causing their stabilization at the synapse by an interaction with GRIP. Importantly, this mechanism is not involved in the constitutive recycling of AMPA receptors since blockade of PDZ interactions can simultaneously increase AMPAR- and decrease KAR-mediated synaptic transmission at the same population of synapses.
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