Department of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, USA.
Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Synapse. 2023 May;77(3):e22264. doi: 10.1002/syn.22264. Epub 2023 Feb 18.
N-methyl-d-aspartate receptors (NMDARs) are calcium-permeable ion channels that are ubiquitously expressed within the glutamatergic postsynaptic density. Phosphorylation of NMDAR subunits defines receptor conductance and surface localization, two alterations that can modulate overall channel activity. Modulation of NMDAR phosphorylation by kinases and phosphatases regulates the amount of calcium entering the cell and subsequent activation of calcium-dependent processes. The dendritic spine enriched protein, spinophilin, is the major synaptic protein phosphatase 1 (PP1) targeting protein. Depending on the substrate, spinophilin can act as either a PP1 targeting protein, to permit substrate dephosphorylation, or a PP1 inhibitory protein, to enhance substrate phosphorylation. Spinophilin limits NMDAR function in a PP1-dependent manner. Specifically, we have previously shown that spinophilin sequesters PP1 away from the GluN2B subunit of the NMDAR, which results in increased phosphorylation of Ser-1284 on GluN2B. However, how spinophilin modifies NMDAR function is unclear. Herein, we utilize a Neuro2A cell line to detail that Ser-1284 phosphorylation increases calcium influx via GluN2B-containing NMDARs. Moreover, overexpression of spinophilin decreases GluN2B-containing NMDAR activity by decreasing its surface expression, an effect that is independent of Ser-1284 phosphorylation. In hippocampal neurons isolated from spinophilin knockout animals, there is an increase in cleaved caspase-3 levels, a marker of calcium-associated apoptosis, compared with wildtype mice. Taken together, our data demonstrate that spinophilin regulates GluN2B containing NMDAR phosphorylation, channel function, and trafficking and that loss of spinophilin enhances neuronal cleaved caspase-3 expression.
N-甲基-D-天冬氨酸受体(NMDARs)是钙通透性离子通道,广泛存在于谷氨酸能突触后密度中。NMDAR 亚基的磷酸化决定了受体的电导和表面定位,这两种改变可以调节整体通道活性。蛋白激酶和磷酸酶对 NMDAR 磷酸化的调节控制着进入细胞的钙量以及随后钙依赖性过程的激活。富含树突棘的蛋白 spinophilin 是主要的突触蛋白磷酸酶 1(PP1)靶向蛋白。根据底物的不同,spinophilin 可以作为 PP1 的靶向蛋白,促进底物去磷酸化,或者作为 PP1 的抑制蛋白,增强底物的磷酸化。Spinophilin 以依赖 PP1 的方式限制 NMDAR 的功能。具体来说,我们之前已经表明,spinophilin 将 PP1 隔离在 NMDAR 的 GluN2B 亚基之外,导致 GluN2B 上 Ser-1284 的磷酸化增加。然而,spinophilin 如何调节 NMDAR 功能尚不清楚。在此,我们利用 Neuro2A 细胞系详细阐明了 Ser-1284 磷酸化通过含有 GluN2B 的 NMDAR 增加钙内流。此外,spinophilin 的过表达通过降低其表面表达来降低含有 GluN2B 的 NMDAR 活性,这种作用独立于 Ser-1284 磷酸化。与野生型小鼠相比,从 spinophilin 敲除动物分离的海马神经元中,cleaved caspase-3 水平(钙相关凋亡的标志物)增加。总之,我们的数据表明,spinophilin 调节含有 GluN2B 的 NMDAR 磷酸化、通道功能和运输,并且 spinophilin 的缺失增强了神经元 cleaved caspase-3 的表达。