致电离效应
神经科学
突触发生
NMDA受体
突触可塑性
谷氨酸受体
突触后电位
长期抑郁
生物
神经可塑性
认知
心理学
受体
AMPA受体
遗传学
作者
Julien P. Dupuis,Olivier Nicole,Laurent Groc
出处
期刊:Neuron
[Elsevier]
日期:2023-08-01
卷期号:111 (15): 2312-2328
被引量:27
标识
DOI:10.1016/j.neuron.2023.05.002
摘要
N-Methyl-D-aspartate ionotropic glutamate receptors (NMDARs) play key roles in synaptogenesis, synaptic maturation, long-term plasticity, neuronal network activity, and cognition. Mirroring this wide range of instrumental functions, abnormalities in NMDAR-mediated signaling have been associated with numerous neurological and psychiatric disorders. Thus, identifying the molecular mechanisms underpinning the physiological and pathological contributions of NMDAR has been a major area of investigation. Over the past decades, a large body of literature has flourished, revealing that the physiology of ionotropic glutamate receptors cannot be restricted to fluxing ions, and involves additional facets controlling synaptic transmissions in health and disease. Here, we review newly discovered dimensions of postsynaptic NMDAR signaling supporting neural plasticity and cognition, such as the nanoscale organization of NMDAR complexes, their activity-dependent redistributions, and non-ionotropic signaling capacities. We also discuss how dysregulations of these processes may directly contribute to NMDAR-dysfunction-related brain diseases.
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