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本文引用的文献

1
Glutamate transporters, EAAT1 and EAAT2, are potentially important in the pathophysiology and treatment of schizophrenia and affective disorders.谷氨酸转运体EAAT1和EAAT2在精神分裂症和情感障碍的病理生理学及治疗中可能具有重要意义。
World J Psychiatry. 2018 Jun 28;8(2):51-63. doi: 10.5498/wjp.v8.i2.51.
2
Myelin Plasticity and Nervous System Function.髓鞘可塑性与神经系统功能
Annu Rev Neurosci. 2018 Jul 8;41:61-76. doi: 10.1146/annurev-neuro-080317-061853.
3
Glutamatergic Signaling in the Central Nervous System: Ionotropic and Metabotropic Receptors in Concert.中枢神经系统中的谷氨酸能信号传导:离子型和代谢型受体协同作用。
Neuron. 2018 Jun 27;98(6):1080-1098. doi: 10.1016/j.neuron.2018.05.018.
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Multiple sclerosis pathogenesis: missing pieces of an old puzzle.多发性硬化症发病机制:旧谜题中的缺失部分。
Rev Neurosci. 2018 Dec 19;30(1):67-83. doi: 10.1515/revneuro-2018-0002.
5
Reduced oligodendrocyte density in layer 5 of the prefrontal cortex in schizophrenia.精神分裂症患者前额叶皮层 5 层的少突胶质细胞密度降低。
Eur Arch Psychiatry Clin Neurosci. 2019 Jun;269(4):379-386. doi: 10.1007/s00406-018-0888-0. Epub 2018 Mar 23.
6
Pharmacogenetic stimulation of neuronal activity increases myelination in an axon-specific manner.药物遗传学刺激神经元活动以轴突特异性方式增加髓鞘形成。
Nat Commun. 2018 Jan 22;9(1):306. doi: 10.1038/s41467-017-02719-2.
7
White Matter Plasticity in the Adult Brain.成人脑的白质可塑性。
Neuron. 2017 Dec 20;96(6):1239-1251. doi: 10.1016/j.neuron.2017.11.026.
8
Axo-myelinic neurotransmission: a novel mode of cell signalling in the central nervous system.轴突-髓鞘神经传递:中枢神经系统中一种新型的细胞信号传导模式。
Nat Rev Neurosci. 2017 Dec 14;19(1):58. doi: 10.1038/nrn.2017.166.
9
On Myelinated Axon Plasticity and Neuronal Circuit Formation and Function.论有髓轴突可塑性与神经元回路的形成及功能
J Neurosci. 2017 Oct 18;37(42):10023-10034. doi: 10.1523/JNEUROSCI.3185-16.2017.
10
Bad wrap: Myelin and myelin plasticity in health and disease.包坏了:髓鞘和髓鞘可塑性在健康和疾病中的作用。
Dev Neurobiol. 2018 Feb;78(2):123-135. doi: 10.1002/dneu.22541. Epub 2017 Oct 17.

谷氨酸转运体:少突胶质细胞中的表达和功能。

Glutamate Transporters: Expression and Function in Oligodendrocytes.

机构信息

Department of Anatomy and Neurobiology, Virginia Commonwealth University School of Medicine, Box 980709, Richmond, VA, 23298, USA.

出版信息

Neurochem Res. 2020 Mar;45(3):551-560. doi: 10.1007/s11064-018-02708-x. Epub 2019 Jan 9.

DOI:10.1007/s11064-018-02708-x
PMID:30628017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6616022/
Abstract

Glutamate, the main excitatory neurotransmitter of the vertebrate central nervous system (CNS), is well known as a regulator of neuronal plasticity and neurodevelopment. Such glutamate function is thought to be mediated primarily by signaling through glutamate receptors. Thus, it requires a tight regulation of extracellular glutamate levels and a fine-tuned homeostasis that, when dysregulated, has been associated with a wide range of central pathologies including neuropsychiatric, neurodevelopmental, and neurodegenerative disorders. In the mammalian CNS, extracellular glutamate levels are controlled by a family of sodium-dependent glutamate transporters belonging to the solute carrier family 1 (SLC1) that are also referred to as excitatory amino acid transporters (EAATs). The presumed main function of EAATs has been best described in the context of synaptic transmission where EAATs expressed by astrocytes and neurons effectively regulate extracellular glutamate levels so that synapses can function independently. There is, however, increasing evidence that EAATs are expressed by cells other than astrocytes and neurons, and that they exhibit functions beyond glutamate clearance. In this review, we will focus on the expression and functions of EAATs in the myelinating cells of the CNS, oligodendrocytes. More specifically, we will discuss potential roles of oligodendrocyte-expressed EAATs in contributing to extracellular glutamate homeostasis, and in regulating oligodendrocyte maturation and CNS myelination by exerting signaling functions that have traditionally been associated with glutamate receptors. In addition, we will provide some examples for how dysregulation of oligodendrocyte-expressed EAATs may be involved in the pathophysiology of neurologic diseases.

摘要

谷氨酸是脊椎动物中枢神经系统(CNS)的主要兴奋性神经递质,作为神经元可塑性和神经发育的调节剂而广为人知。这种谷氨酸功能被认为主要通过谷氨酸受体信号传导来介导。因此,它需要严格调节细胞外谷氨酸水平和精细的动态平衡,当这种平衡失调时,与广泛的中枢病理学有关,包括神经精神疾病、神经发育和神经退行性疾病。在哺乳动物的中枢神经系统中,细胞外谷氨酸水平由属于溶质载体家族 1(SLC1)的一组钠依赖性谷氨酸转运体家族控制,这些转运体也被称为兴奋性氨基酸转运体(EAATs)。EAATs 的假定主要功能在突触传递的背景下得到了最好的描述,星形胶质细胞和神经元表达的 EAATs 有效地调节细胞外谷氨酸水平,以使突触能够独立发挥功能。然而,越来越多的证据表明,EAATs 不仅在星形胶质细胞和神经元中表达,而且具有谷氨酸清除以外的功能。在这篇综述中,我们将重点介绍 EAAT 在中枢神经系统髓鞘形成细胞——少突胶质细胞中的表达和功能。更具体地说,我们将讨论少突胶质细胞表达的 EAAT 在维持细胞外谷氨酸稳态、调节少突胶质细胞成熟和中枢神经系统髓鞘形成方面的潜在作用,通过发挥传统上与谷氨酸受体相关的信号功能。此外,我们将提供一些例子,说明少突胶质细胞表达的 EAAT 失调如何参与神经疾病的病理生理学。