Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, 4072, Australia.
Sci China Life Sci. 2014 Apr;57(4):403-11. doi: 10.1007/s11427-014-4637-y. Epub 2014 Mar 14.
New neurons are continuously generated from resident pools of neural stem and precursor cells (NSPCs) in the adult brain. There are multiple pathways through which adult neurogenesis is regulated, and here we review the role of the N-methyl-D-aspartate receptor (NMDAR) in regulating the proliferation of NSPCs in the adult hippocampus. Hippocampal-dependent learning tasks, enriched environments, running, and activity-dependent synaptic plasticity, all potently up-regulate hippocampal NSPC proliferation. We first consider the requirement of the NMDAR in activity-dependent synaptic plasticity, and the role the induction of synaptic plasticity has in regulating NSPCs and newborn neurons. We address how specific NMDAR agonists and antagonists modulate proliferation, both in vivo and in vitro, and then review the evidence supporting the hypothesis that NMDARs are present on NSPCs. We believe it is important to understand the mechanisms underlying the activation of adult neurogenesis, given the potential that endogenous stem cell populations have for repopulating the hippocampus with functional new neurons. In conditions such as age-related memory decline, neurodegeneration and psychiatric disease, mature neurons are lost or become defective; as such, stimulating adult neurogenesis may provide a therapeutic strategy to overcome these conditions.
新的神经元不断地从成年大脑中常驻的神经干细胞和前体细胞(NSPCs)池中产生。有多种途径可以调节成年神经发生,在这里我们回顾了 N-甲基-D-天冬氨酸受体(NMDAR)在调节成年海马体中 NSPC 增殖中的作用。海马体依赖的学习任务、丰富的环境、跑步和依赖于活动的突触可塑性,都能强烈地上调海马体 NSPC 的增殖。我们首先考虑 NMDAR 在依赖于活动的突触可塑性中的要求,以及诱导突触可塑性在调节 NSPC 和新生神经元中的作用。我们探讨了特定的 NMDAR 激动剂和拮抗剂如何在体内和体外调节增殖,然后回顾了支持 NMDAR 存在于 NSPC 上的假说的证据。我们认为,了解激活成年神经发生的机制非常重要,因为内源性干细胞群有可能用功能性的新神经元重新填充海马体。在与年龄相关的记忆减退、神经退行性变和精神疾病等情况下,成熟神经元会丢失或出现缺陷;因此,刺激成年神经发生可能是克服这些情况的一种治疗策略。