Djavad Mowafaghian Centre for Brain Health and Department of Medicine, University of British Columbia, Vancouver, BC, Canada, V6T 2B5.
Djavad Mowafaghian Centre for Brain Health and Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada, V6T 2B5.
Nat Commun. 2019 Sep 9;10(1):4089. doi: 10.1038/s41467-019-12096-7.
The α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid subtype glutamate receptors (AMPARs) mediate the fast excitatory synaptic transmission in the mammalian brain and are important for synaptic plasticity. In particular, the rapid insertion of the GluA1 homomeric (GluA1-homo) AMPARs into the postsynaptic membrane is considered to be critical in the expression of hippocampal CA1 long-term potentiation (LTP), which is important for certain forms of learning and memory. However, how the formation and trafficking of GluA1-homo AMPARs are regulated remains poorly understood. Here, we report that p97 specifically interacts with and promotes the formation of GluA1-homo AMPARs. The association with p97 retains GluA1-homo AMPARs in the intracellular compartment under basal conditions, and its dissociation allows GluA1-homo AMPARs to be rapidly inserted into the postsynaptic membrane shortly after LTP induction. Thus, our results shed lights into the molecular mechanisms by which p97 regulates GluA1-homo AMPARs formation and trafficking, thereby playing a critical role in mediating synaptic plasticity.
α-氨基-3-羟基-5-甲基异恶唑-4-丙酸型谷氨酸受体(AMPARs)介导哺乳动物大脑中的快速兴奋性突触传递,对于突触可塑性很重要。特别是,GluA1 同型(GluA1-homo)AMPAR 的快速插入到突触后膜被认为是海马 CA1 长时程增强(LTP)表达的关键,这对于某些形式的学习和记忆很重要。然而,GluA1-homo AMPAR 的形成和运输如何受到调节仍知之甚少。在这里,我们报告 p97 特异性地与 GluA1-homo AMPAR 相互作用并促进其形成。在基础条件下,与 p97 的关联将 GluA1-homo AMPAR 保留在细胞内隔室中,其解离允许 GluA1-homo AMPAR 在 LTP 诱导后不久迅速插入到突触后膜中。因此,我们的结果揭示了 p97 调节 GluA1-homo AMPAR 形成和运输的分子机制,从而在介导突触可塑性中发挥关键作用。