Ependymal cells: roles in central nervous system infections and therapeutic application.

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Shiqi Xie, Feng Li
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引用次数: 0

Abstract

Ependymal cells are arranged along the inner surfaces of the ventricles and the central canal of the spinal cord, providing anatomical, physiological and immunological barriers that maintain cerebrospinal fluid (CSF) homeostasis. Based on this, studies have found that alterations in gene expression, cell junctions, cytokine secretion and metabolic disturbances can lead to dysfunction of ependymal cells, thereby participating in the onset and progression of central nervous system (CNS) infections. Additionally, ependymal cells can exhibit proliferative and regenerative potential as well as secretory functions during CNS injury, contributing to neuroprotection and post-injury recovery. Currently, studies on ependymal cell primarily focus on the basic investigations of their morphology, function and gene expression; however, there is a notable lack of clinical translational studies examining the molecular mechanisms by which ependymal cells are involved in disease onset and progression. This limits our understanding of ependymal cells in CNS infections and the development of therapeutic applications. Therefore, this review will discuss the molecular mechanism underlying the involvement of ependymal cells in CNS infections, and explore their potential for application in clinical treatment modalities.

上皮细胞:在中枢神经系统感染中的作用和治疗应用。
外膜细胞沿脑室和脊髓中央管的内表面排列,提供解剖学、生理学和免疫学屏障,维持脑脊液(CSF)的平衡。在此基础上,研究发现基因表达、细胞连接、细胞因子分泌和新陈代谢紊乱的改变可导致附腱鞘细胞功能失调,从而参与中枢神经系统(CNS)感染的发生和发展。此外,在中枢神经系统损伤期间,附腱鞘细胞可表现出增殖和再生潜能以及分泌功能,有助于神经保护和损伤后恢复。目前,对附膈膜细胞的研究主要集中在对其形态、功能和基因表达的基础研究上;然而,对附膈膜细胞参与疾病发生和发展的分子机制的临床转化研究却明显不足。这限制了我们对中枢神经系统感染中的附红细胞的了解和治疗应用的开发。因此,本综述将讨论附红细胞参与中枢神经系统感染的分子机制,并探讨其在临床治疗模式中的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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