Section on Molecular Neurobiology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
Int J Mol Sci. 2023 Feb 2;24(3):2908. doi: 10.3390/ijms24032908.
Neuregulins (NRGs) signal via ErbB receptors to regulate neural development, excitability, synaptic and network activity, and behaviors relevant to psychiatric disorders. Bidirectional signaling between NRG2/ErbB4 and NMDA receptors is thought to homeostatically regulate GABAergic interneurons in response to increased excitatory neurotransmission or elevated extracellular glutamate levels. Unprocessed proNRG2 forms discrete clusters on cell bodies and proximal dendrites that colocalize with the potassium channel Kv2.1 at specialized endoplasmic reticulum-plasma membrane (ER-PM) junctions, and NMDA receptor activation triggers rapid dissociation from ER-PM junctions and ectodomain shedding by ADAM10. Here, we elucidate the mechanistic basis of proNRG2 clustering at ER-PM junctions and its regulation by NMDA receptors. Importantly, we demonstrate that proNRG2 promotes the formation of ER-PM junctions by directly binding the ER-resident membrane tether VAP, like Kv2.1. The proNRG2 intracellular domain harbors two non-canonical, low-affinity sites that cooperatively mediate VAP binding. One of these is a cryptic and phosphorylation-dependent VAP binding motif that is dephosphorylated following NMDA receptor activation, thus revealing how excitatory neurotransmission promotes the dissociation of proNRG2 from ER-PM junctions. Therefore, proNRG2 and Kv2.1 can independently function as VAP-dependent organizers of neuronal ER-PM junctions. Based on these and prior studies, we propose that proNRG2 and Kv2.1 serve as co-regulated downstream effectors of NMDA receptors to homeostatically regulate GABAergic interneurons.
神经调节素(NRGs)通过 ErbB 受体发出信号,调节神经发育、兴奋性、突触和网络活动以及与精神障碍相关的行为。NRG2/ErbB4 和 NMDA 受体之间的双向信号传递被认为可以通过内稳态调节 GABA 能中间神经元,以响应增加的兴奋性神经传递或升高的细胞外谷氨酸水平。未加工的 proNRG2 以离散的簇的形式存在于细胞体和近端树突上,与钾通道 Kv2.1 共定位在专门的内质网-质膜(ER-PM)连接处,NMDA 受体的激活触发 proNRG2 从 ER-PM 连接处快速解离,并通过 ADAM10 进行外显子脱落。在这里,我们阐明了 proNRG2 在 ER-PM 连接处聚集的机制基础及其受 NMDA 受体的调节。重要的是,我们证明 proNRG2 通过直接与 ER 驻留膜拴系蛋白 VAP 结合来促进 ER-PM 连接处的形成,就像 Kv2.1 一样。proNRG2 细胞内结构域包含两个非典型的、低亲和力的位点,它们协同介导 VAP 结合。其中一个是一个隐藏的、依赖于磷酸化的 VAP 结合基序,在 NMDA 受体激活后去磷酸化,从而揭示了兴奋性神经传递如何促进 proNRG2 从 ER-PM 连接处解离。因此,proNRG2 和 Kv2.1 可以独立作为神经元 ER-PM 连接处的 VAP 依赖性组织者发挥作用。基于这些和之前的研究,我们提出 proNRG2 和 Kv2.1 作为 NMDA 受体的共同调节下游效应物,以通过内稳态调节 GABA 能中间神经元。