Yu GuiLian, Zhang Ying, Ning Bin
Jinan Central Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Front Cell Neurosci. 2021 Dec 23;15:792764. doi: 10.3389/fncel.2021.792764. eCollection 2021.
Traumatic central nervous system (CNS) injury, which includes both traumatic brain injury (TBI) and spinal cord injury (SCI), is associated with irreversible loss of neurological function and high medical care costs. Currently, no effective treatment exists to improve the prognosis of patients. Astrocytes comprise the largest population of glial cells in the CNS and, with the advancements in the field of neurology, are increasingly recognized as having key functions in both the brain and the spinal cord. When stimulated by disease or injury, astrocytes become activated and undergo a series of changes, including alterations in gene expression, hypertrophy, the loss of inherent functions, and the acquisition of new ones. Studies have shown that astrocytes are highly heterogeneous with respect to their gene expression profiles, and this heterogeneity accounts for their observed context-dependent phenotypic diversity. In the inured CNS, activated astrocytes play a dual role both as regulators of neuroinflammation and in scar formation. Identifying the subpopulations of reactive astrocytes that exert beneficial or harmful effects will aid in deciphering the pathological mechanisms underlying CNS injuries and ultimately provide a theoretical basis for the development of effective strategies for the treatment of associated conditions. Following CNS injury, as the disease progresses, astrocyte phenotypes undergo continuous changes. Although current research methods do not allow a comprehensive and accurate classification of astrocyte subpopulations in complex pathological contexts, they can nonetheless aid in understanding the roles of astrocytes in disease. In this review, after a brief introduction to the pathology of CNS injury, we summarize current knowledge regarding astrocyte activation following CNS injury, including: (a) the regulatory factors involved in this process; (b) the functions of different astrocyte subgroups based on the existing classification of astrocytes; and (c) attempts at astrocyte-targeted therapy.
创伤性中枢神经系统(CNS)损伤,包括创伤性脑损伤(TBI)和脊髓损伤(SCI),与神经功能的不可逆丧失和高昂的医疗费用相关。目前,尚无有效的治疗方法来改善患者的预后。星形胶质细胞是中枢神经系统中数量最多的胶质细胞群体,随着神经学领域的发展,它们在脑和脊髓中的关键功能越来越受到认可。当受到疾病或损伤刺激时,星形胶质细胞会被激活并发生一系列变化,包括基因表达改变、肥大、固有功能丧失以及获得新功能。研究表明,星形胶质细胞在基因表达谱方面具有高度异质性,这种异质性解释了它们所观察到的依赖于环境的表型多样性。在受损的中枢神经系统中,活化的星形胶质细胞在神经炎症调节和瘢痕形成中都发挥着双重作用。识别发挥有益或有害作用的确性星形胶质细胞亚群,将有助于阐明中枢神经系统损伤的病理机制,并最终为开发相关疾病的有效治疗策略提供理论依据。中枢神经系统损伤后,随着疾病进展,星形胶质细胞表型会持续变化。虽然目前的研究方法无法在复杂病理环境中对星形胶质细胞亚群进行全面准确的分类,但它们仍有助于理解星形胶质细胞在疾病中的作用。在本综述中,在简要介绍中枢神经系统损伤的病理学之后,我们总结了目前关于中枢神经系统损伤后星形胶质细胞活化的知识,包括:(a)参与这一过程的调节因子;(b)基于现有星形胶质细胞分类的不同星形胶质细胞亚群的功能;以及(c)针对星形胶质细胞的治疗尝试。