Sagol Department of Neurobiology, Faculty of Natural Sciences, University of Haifa, Haifa 3103301, Israel.
Center for Rare Diseases, Emek Medical Center, Afula 1834111, Israel.
Int J Mol Sci. 2024 Nov 18;25(22):12366. doi: 10.3390/ijms252212366.
N-methyl-D-aspartate receptors (NMDARs) are critical components of the mammalian central nervous system, involved in synaptic transmission, plasticity, and neurodevelopment. This review focuses on the structural and functional characteristics of NMDARs, with a particular emphasis on the GRIN2 subunits (GluN2A-D). The diversity of GRIN2 subunits, driven by alternative splicing and genetic variants, significantly impacts receptor function, synaptic localization, and disease manifestation. The temporal and spatial expression of these subunits is essential for typical neural development, with each subunit supporting distinct phases of synaptic formation and plasticity. Disruptions in their developmental regulation are linked to neurodevelopmental disorders, underscoring the importance of understanding these dynamics in NDD pathophysiology. We explore the physiological properties and developmental regulation of these subunits, highlighting their roles in the pathophysiology of various NDDs, including ASD, epilepsy, and schizophrenia. By reviewing current knowledge and experimental models, including mouse models and human-induced pluripotent stem cells (hiPSCs), this article aims to elucidate different approaches through which the intricacies of NMDAR dysfunction in NDDs are currently being explored. The comprehensive understanding of NMDAR subunit composition and their mutations provides a foundation for developing targeted therapeutic strategies to address these complex disorders.
N-甲基-D-天冬氨酸受体(NMDARs)是哺乳动物中枢神经系统的关键组成部分,参与突触传递、可塑性和神经发育。本综述重点介绍了 NMDAR 的结构和功能特性,特别关注 GRIN2 亚基(GluN2A-D)。GRIN2 亚基的多样性由选择性剪接和遗传变异驱动,对受体功能、突触定位和疾病表现有重大影响。这些亚基的时空表达对典型的神经发育至关重要,每个亚基支持突触形成和可塑性的不同阶段。它们在发育调节中的紊乱与神经发育障碍有关,这凸显了在 NDD 病理生理学中理解这些动态的重要性。我们探讨了这些亚基的生理特性和发育调节,强调了它们在各种 NDD (包括 ASD、癫痫和精神分裂症)的病理生理学中的作用。通过回顾当前的知识和实验模型,包括小鼠模型和人类诱导多能干细胞(hiPSCs),本文旨在阐明目前正在探索 NDD 中 NMDAR 功能障碍的不同方法。对 NMDAR 亚基组成及其突变的全面了解为开发针对这些复杂疾病的靶向治疗策略提供了基础。