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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Zinc transporter-1: a novel NMDA receptor-binding protein at the postsynaptic density
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Zinc transporter-1: a novel NMDA receptor-binding protein at the postsynaptic density

机译:锌转运蛋白-1:突触后密度的新型NMDA受体结合蛋白。

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Zinc (Zn2+) is believed to play a relevant role in the physiology and pathophysiology of the brain. Hence, Zn2+ homeostasis is critical and involves different classes of molecules, including Zn2+ transporters. The ubiquitous Zn2+ transporter-1 (ZNT-1) is a transmembrane protein that pumps cytosolic Zn2+ to the extracellular space, but its function in the central nervous system is not fully understood. Here, we show that ZNT-1 interacts with GluN2A-containing NMDA receptors, suggesting a role for this transporter at the excitatory glutamatergic synapse. First, we found that ZNT-1 is highly expressed at the hippocampal postsynaptic density (PSD) where NMDA receptors are enriched. Two-hybrid screening, coimmunoprecipitation experiments and clustering assay in COS-7 cells demonstrated that ZNT-1 specifically binds the GluN2A subunit of the NMDA receptor. GluN2A deletion mutants and pull-down assays indicated GluN2A(1390-1464) domain as necessary for the binding to ZNT-1. Most importantly, ZNT-1/GluN2A complex was proved to be dynamic, since it was regulated by induction of synaptic plasticity. Finally, modulation of ZNT-1 expression in hippocampal neurons determined a significant change in dendritic spine morphology, PSD-95 clusters and GluN2A surface levels, supporting the involvement of ZNT-1 in the dynamics of excitatory PSD.
机译:锌(Zn2 +)被认为在大脑的生理和病理生理中起着重要的作用。因此,Zn2 +稳态至关重要,并且涉及不同种类的分子,包括Zn2 +转运蛋白。普遍存在的Zn2 +转运蛋白-1(ZNT-1)是一种跨膜蛋白,可将胞浆中的Zn2 +泵送到细胞外空间,但其在中枢神经系统中的功能尚不完全清楚。在这里,我们显示ZNT-1与包含GluN2A的NMDA受体相互作用,表明该转运蛋白在兴奋性谷氨酸能突触中的作用。首先,我们发现ZNT-1在NMDA受体富集的海马突触后密度(PSD)上高表达。 COS-7细胞中的两个杂交筛选,免疫沉淀实验和聚类分析表明ZNT-1特异性结合NMDA受体的GluN2A亚基。 GluN2A缺失突变体和下拉分析表明,GluN2A(1390-1464)域是与ZNT-1结合所必需的。最重要的是,事实证明ZNT-1 / GluN2A复合物是动态的,因为它是通过诱导突触可塑性来调节的。最后,海马神经元中ZNT-1表达的调节决定了树突棘形态,PSD-95簇和GluN2A表面水平的显着变化,支持ZNT-1参与了兴奋性PSD的动力学。

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