Mellor J R
MRC Centre for Synaptic Plasticity, Department of Anatomy, University of Bristol, Bristol BS8 1TD, UK.
Biochem Soc Trans. 2006 Nov;34(Pt 5):949-51. doi: 10.1042/BST0340949.
Synaptic plasticity of ionotropic glutamate receptors has been extensively studied with a particular focus on the role played by NMDA (N-methyl-D-aspartate) receptors in the induction of synaptic plasticity and the subsequent movement of AMPA (alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid) receptors. The third subtype of ionotropic glutamate receptor, kainate receptors, has not been studied to the same extent, but recent evidence shows that these receptors also exhibit synaptic plasticity in response to activity. There is also a growing body of data on the mechanisms underlying kainate receptor trafficking and the proteins they interact with. This review summarizes the current state of knowledge on this topic, focusing on the evidence for the removal or insertion of functional kainate receptors in response to synaptic activity and the cellular mechanisms that underlie this regulation of neuronal kainate receptor function.
离子型谷氨酸受体的突触可塑性已得到广泛研究,特别关注N-甲基-D-天冬氨酸(NMDA)受体在突触可塑性诱导以及随后α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)受体移动中所起的作用。离子型谷氨酸受体的第三种亚型,即海人藻酸受体,尚未得到同等程度的研究,但最近的证据表明,这些受体在对活动作出反应时也表现出突触可塑性。关于海人藻酸受体转运的潜在机制以及它们与之相互作用的蛋白质的数据也越来越多。本综述总结了关于该主题的当前知识状态,重点关注响应突触活动时功能性海人藻酸受体的去除或插入的证据以及神经元海人藻酸受体功能调节的细胞机制。