星形胶质细胞在中风诱导的神经退行性变中的作用:时间轴

Frontiers in molecular medicine Pub Date : 2023-09-07 eCollection Date: 2023-01-01 DOI:10.3389/fmmed.2023.1240862
Eileen Collyer, Elena Blanco-Suarez
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引用次数: 0

摘要

中风是一种以大脑某一区域的血流量突然中断为特征的疾病,并由不同的损伤后阶段定义,其中涉及各种分子和细胞级联反应。在急性期的早期阶段,发生快速的初始细胞死亡,随后发生炎症和瘢痕形成。随后是亚急性或恢复期,此时内源性可塑性机制可能促进自发恢复,这取决于各种尚未完全了解的因素。在较晚的时间点,在临床和临床前研究中,与健康对照相比,中风导致更大的神经退行性变,这在恢复缓慢和神经退行性特征出现的慢性期是明显的。由于星形胶质细胞在谷氨酸再摄取中的作用,作为神经血管单元的组成部分,作为胶质瘢痕的构建块和突触可塑性调节剂,在缺血性中风的背景下进行了研究。所有这些作用使得星形胶质细胞在中风诱导的神经退行性变的背景下变得有趣,但尚未得到充分研究。在这篇综述中,我们对以往的研究进行了总结,强调星形胶质细胞是潜在的治疗靶点,并提出了星形胶质细胞在急性、亚急性和慢性中风后阶段可能导致神经恢复或神经退行性变的机制中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Astrocytes in stroke-induced neurodegeneration: a timeline.

Stroke is a condition characterized by sudden deprivation of blood flow to a brain region and defined by different post-injury phases, which involve various molecular and cellular cascades. At an early stage during the acute phase, fast initial cell death occurs, followed by inflammation and scarring. This is followed by a sub-acute or recovery phase when endogenous plasticity mechanisms may promote spontaneous recovery, depending on various factors that are yet to be completely understood. At later time points, stroke leads to greater neurodegeneration compared to healthy controls in both clinical and preclinical studies, this is evident during the chronic phase when recovery slows down and neurodegenerative signatures appear. Astrocytes have been studied in the context of ischemic stroke due to their role in glutamate re-uptake, as components of the neurovascular unit, as building blocks of the glial scar, and synaptic plasticity regulators. All these roles render astrocytes interesting, yet understudied players in the context of stroke-induced neurodegeneration. With this review, we provide a summary of previous research, highlight astrocytes as potential therapeutic targets, and formulate questions about the role of astrocytes in the mechanisms during the acute, sub-acute, and chronic post-stroke phases that may lead to neurorestoration or neurodegeneration.

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