Hardingham Giles
UK Dementia Research Institute, University of Edinburgh, Edinburgh, EH16 4TJ, UK.
Centre for Discovery Brain Sciences, Edinburgh Medical School, University of Edinburgh, Edinburgh, EH8 9XD, UK.
F1000Res. 2019 Aug 30;8. doi: 10.12688/f1000research.19925.1. eCollection 2019.
The NMDA subtype of ionotropic glutamate receptor is a sophisticated integrator and transducer of information. NMDAR-mediated signals control diverse processes across the life course, including synaptogenesis and synaptic plasticity, as well as contribute to excitotoxic processes in neurological disorders. At the basic biophysical level, the NMDAR is a coincidence detector, requiring the co-presence of agonist, co-agonist, and membrane depolarization in order to open. However, the NMDAR is not merely a conduit for ions to flow through; it is linked on the cytoplasmic side to a large network of signaling and scaffolding proteins, primarily via the C-terminal domain of NMDAR GluN2 subunits. These physical interactions help to organize the signaling cascades downstream of NMDAR activation. Notably, the NMDAR does not come in a single form: the subunit composition of the NMDAR, particularly the GluN2 subunit subtype (GluN2A-D), influences the biophysical properties of the channel. Moreover, a growing number of studies have illuminated the extent to which GluN2 C-terminal interactions vary according to GluN2 subtype and how this impacts on the processes that NMDAR activity controls. We will review recent advances, controversies, and outstanding questions in this active area of research.
离子型谷氨酸受体的NMDA亚型是一种复杂的信息整合器和转换器。NMDAR介导的信号控制着整个生命过程中的各种过程,包括突触发生和突触可塑性,并且在神经疾病的兴奋性毒性过程中也发挥作用。在基本生物物理层面,NMDAR是一种巧合探测器,需要激动剂、共激动剂和膜去极化同时存在才能打开。然而,NMDAR不仅仅是离子流动的通道;它在细胞质一侧主要通过NMDAR GluN2亚基的C末端结构域与大量信号和支架蛋白网络相连。这些物理相互作用有助于组织NMDAR激活下游的信号级联反应。值得注意的是,NMDAR并非单一形式:NMDAR的亚基组成,特别是GluN2亚基亚型(GluN2A-D),会影响通道的生物物理特性。此外,越来越多的研究揭示了GluN2 C末端相互作用根据GluN2亚型的变化程度以及这如何影响NMDAR活性所控制的过程。我们将综述这一活跃研究领域的最新进展、争议和悬而未决的问题。