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Synaptic GluN2A-Containing NMDA Receptors: From Physiology to Pathological Synaptic Plasticity

机译:突触Glun2a的NMDA受体:从生理到病理突触可塑性

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N-Methyl- d -Aspartate Receptors (NMDARs) are ionotropic glutamate-gated receptors. NMDARs are tetramers composed by several homologous subunits of GluN1-, GluN2-, or GluN3-type, leading to the existence in the central nervous system of a high variety of receptor subtypes with different pharmacological and signaling properties. NMDAR subunit composition is strictly regulated during development and by activity-dependent synaptic plasticity. Given the differences between GluN2 regulatory subunits of NMDAR in several functions, here we will focus on the synaptic pool of NMDARs containing the GluN2A subunit, addressing its role in both physiology and pathological synaptic plasticity as well as the contribution in these events of different types of GluN2A-interacting proteins.
机译:N-甲基-D-海地酸盐受体(NMDARS)是离子型谷氨酸的受体。 NMDAR是由Glun1-,Glun2-或Glun3型的几种同源亚基组成的四聚体,导致具有不同药理学和信号性质的高种受体亚型的中枢神经系统存在。 NMDAR亚基组合物在开发过程中严格调节,并通过活性依赖性突触可塑性。鉴于几种职能的NMDAR的Glun2监管亚基的差异,我们将重点关注含有Glun2A亚基的NMDARS的突触池,解决其在生理学和病理突触塑性的作用以及这些不同类型的事件中的贡献GLUN2A-相互作用的蛋白质。

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