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促红细胞生成素/红细胞生成素受体与兴奋性氨基酸受体之间的相互作用:在突触可塑性调节及神经元变性病理生理学中的潜在关联。

Interaction between ephrins/Eph receptors and excitatory amino acid receptors: possible relevance in the regulation of synaptic plasticity and in the pathophysiology of neuronal degeneration.

作者信息

Calò Laura, Cinque Carlo, Patanè Monica, Schillaci Danilo, Battaglia Giuseppe, Melchiorri Daniela, Nicoletti Ferdinando, Bruno Valeria

机构信息

Department of Human Physiology and Pharmacology, University La Sapienza, Rome, Italy.

出版信息

J Neurochem. 2006 Jul;98(1):1-10. doi: 10.1111/j.1471-4159.2006.03844.x.

DOI:10.1111/j.1471-4159.2006.03844.x
PMID:16805791
Abstract

There is increasing evidence that Eph receptors and their transmembrane ligands, named ephrins, interact with glutamate receptors in both developing and adult neurons. EphB receptors interact with proteins that regulate the membrane trafficking of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate (AMPA) receptor subunits, and both ephrins and EphB receptors have been found to co-localize with N-methyl-d-aspartate (NMDA) receptors and to positively modulate NMDA receptor function. Moreover, pharmacologic activation of ephrin-Bs amplifies group-I metabotropic glutamate receptor signaling through mechanisms that involve NMDA receptors. The interaction with ionotropic or metabotropic glutamate receptors provides a substrate for the emerging role of ephrins and Eph receptors in the regulation of activity-dependent forms of synaptic plasticity, such as long-term potentiation and long-term depression, which are established electrophysiologic models of associative learning. In addition, these interactions explain the involvement of ephrins/Eph receptors in the regulation of pain threshold and epileptogenesis, as well as their potential implication in processes of neuronal degeneration. This may stimulate the search for new drugs that might modulate excitatory synaptic transmission by interacting with the ephrin/Eph receptor system.

摘要

越来越多的证据表明,Eph受体及其跨膜配体(称为ephrin)在发育中的神经元和成熟神经元中均与谷氨酸受体相互作用。EphB受体与调节α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)受体亚基膜转运的蛋白质相互作用,并且已发现ephrin和EphB受体均与N-甲基-D-天冬氨酸(NMDA)受体共定位,并正向调节NMDA受体功能。此外,ephrin-B的药理学激活通过涉及NMDA受体的机制增强I型代谢型谷氨酸受体信号传导。与离子型或代谢型谷氨酸受体的相互作用为ephrin和Eph受体在调节依赖活动的突触可塑性形式(如长期增强和长期抑制,它们是联想学习的既定电生理模型)中发挥新作用提供了基础。此外,这些相互作用解释了ephrin/Eph受体在疼痛阈值调节和癫痫发生中的作用,以及它们在神经元变性过程中的潜在影响。这可能会刺激人们寻找通过与ephrin/Eph受体系统相互作用来调节兴奋性突触传递的新药。

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