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Glutamate transporters: Critical components of glutamatergic transmission

兴奋毒性 谷氨酸的 谷氨酸受体 生物 神经科学 神经传递 运输机 代谢型谷氨酸受体 突触裂 NMDA受体 细胞生物学 受体 生物化学 基因
作者
Ada G. Rodríguez-Campuzano,Arturo Ortega
出处
期刊:Neuropharmacology [Elsevier]
卷期号:192: 108602-108602 被引量:33
标识
DOI:10.1016/j.neuropharm.2021.108602
摘要

Glutamate is the major excitatory neurotransmitter in the vertebrate central nervous system. Once released, it binds to specific membrane receptors and transporters activating a wide variety of signal transduction cascades, as well as its removal from the synaptic cleft in order to avoid its extracellular accumulation and the overstimulation of extra-synaptic receptors that might result in neuronal death through a process known as excitotoxicity. Although neurodegenerative diseases are heterogenous in clinical phenotypes and genetic etiologies, a fundamental mechanism involved in neuronal degeneration is excitotoxicity. Glutamate homeostasis is critical for brain physiology and Glutamate transporters are key players in maintaining low extracellular Glutamate levels. Therefore, the characterization of Glutamate transporters has been an active area of glutamatergic research for the last 40 years. Transporter activity its regulated at different levels: transcriptional and translational control, transporter protein trafficking and membrane mobility, and through extensive post-translational modifications. The elucidation of these mechanisms has emerged as an important piece to shape our current understanding of glutamate actions in the nervous system.
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