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星形胶质细胞衍生的生长因子与雌激素神经保护作用:转化生长因子-α在雌激素诱导星形胶质细胞中谷氨酸转运体上调中的作用

Astrocyte-derived growth factors and estrogen neuroprotection: role of transforming growth factor-α in estrogen-induced upregulation of glutamate transporters in astrocytes.

作者信息

Karki Pratap, Smith Keisha, Johnson James, Lee Eunsook

机构信息

Department of Physiology, School of Medicine, Meharry Medical College, Nashville, TN, USA.

Department of Physiology, School of Medicine, Meharry Medical College, Nashville, TN, USA.

出版信息

Mol Cell Endocrinol. 2014 May 25;389(1-2):58-64. doi: 10.1016/j.mce.2014.01.010. Epub 2014 Jan 18.

DOI:10.1016/j.mce.2014.01.010
PMID:24447465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4040305/
Abstract

Extensive studies from the past decade have completely revolutionized our understanding about the role of astrocytes in the brain from merely supportive cells to an active role in various physiological functions including synaptic transmission via cross-talk with neurons and neuroprotection via releasing neurotrophic factors. Particularly, numerous studies have reported that astrocytes mediate the neuroprotective effects of 17β-estradiol (E2) and selective estrogen receptor modulators (SERMs) in various clinical and experimental models of neuronal injury. Astrocytes contain two main glutamate transporters, glutamate aspartate transporter (GLAST) and glutamate transporter-1 (GLT-1), that play a key role in preventing excitotoxic neuronal death, a process associated with most neurodegenerative diseases. E2 has been shown to increase expression of both GLAST and GLT-1 mRNA and protein and glutamate uptake in astrocytes. Growth factors such as transforming growth factor-α (TGF-α) appear to mediate E2-induced enhancement of these transporters. These findings suggest that E2 exerts neuroprotection against excitotoxic neuronal injuries, at least in part, by enhancing astrocytic glutamate transporter levels and function. Therefore, the present review will discuss proposed mechanisms involved in astrocyte-mediated E2 neuroprotection, with a focus on glutamate transporters.

摘要

过去十年的广泛研究彻底改变了我们对星形胶质细胞在大脑中作用的理解,从仅仅是支持性细胞转变为在各种生理功能中发挥积极作用,包括通过与神经元的相互作用参与突触传递以及通过释放神经营养因子实现神经保护。特别是,大量研究报告称,在各种神经元损伤的临床和实验模型中,星形胶质细胞介导了17β-雌二醇(E2)和选择性雌激素受体调节剂(SERMs)的神经保护作用。星形胶质细胞含有两种主要的谷氨酸转运体,即谷氨酸天冬氨酸转运体(GLAST)和谷氨酸转运体-1(GLT-1),它们在预防兴奋性毒性神经元死亡中起关键作用,而兴奋性毒性神经元死亡是与大多数神经退行性疾病相关的过程。E2已被证明可增加星形胶质细胞中GLAST和GLT-1 mRNA及蛋白的表达以及谷氨酸摄取。诸如转化生长因子-α(TGF-α)等生长因子似乎介导了E2诱导的这些转运体的增强。这些发现表明,E2至少部分地通过提高星形胶质细胞谷氨酸转运体水平和功能来对兴奋性毒性神经元损伤发挥神经保护作用。因此,本综述将讨论星形胶质细胞介导的E2神经保护作用的相关机制,重点关注谷氨酸转运体。

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