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胶质细胞作为与多发性硬化症相关的神经炎症机制中的关键调节者。

Glial Cells as Key Regulators in Neuroinflammatory Mechanisms Associated with Multiple Sclerosis.

机构信息

Neuroscience Department, The Cyprus Institute of Neurology and Genetics, 2371 Nicosia, Cyprus.

Center for Multiple Sclerosis and Related Disorders, The Cyprus Institute of Neurology and Genetics, 2371 Nicosia, Cyprus.

出版信息

Int J Mol Sci. 2024 Sep 4;25(17):9588. doi: 10.3390/ijms25179588.

Abstract

Even though several highly effective treatments have been developed for multiple sclerosis (MS), the underlying pathological mechanisms and drivers of the disease have not been fully elucidated. In recent years, there has been a growing interest in studying neuroinflammation in the context of glial cell involvement as there is increasing evidence of their central role in disease progression. Although glial cell communication and proper function underlies brain homeostasis and maintenance, their multiple effects in an MS brain remain complex and controversial. In this review, we aim to provide an overview of the contribution of glial cells, oligodendrocytes, astrocytes, and microglia in the pathology of MS during both the activation and orchestration of inflammatory mechanisms, as well as of their synergistic effects during the repair and restoration of function. Additionally, we discuss how the understanding of glial cell involvement in MS may provide new therapeutic targets either to limit disease progression or to facilitate repair.

摘要

尽管已经开发出了几种针对多发性硬化症(MS)的高效治疗方法,但该疾病的潜在病理机制和驱动因素尚未完全阐明。近年来,人们越来越关注研究神经炎症在神经胶质细胞参与下的情况,因为越来越多的证据表明它们在疾病进展中起着核心作用。尽管神经胶质细胞的通讯和正常功能是大脑内环境稳定和维持的基础,但它们在 MS 大脑中的多种作用仍然复杂且存在争议。在这篇综述中,我们旨在概述神经胶质细胞(少突胶质细胞、星形胶质细胞和小胶质细胞)在激活和协调炎症机制期间以及在修复和恢复功能期间的协同作用,在 MS 病理学中的贡献。此外,我们还讨论了了解神经胶质细胞在 MS 中的参与如何为限制疾病进展或促进修复提供新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7817/11395575/f2b8d6a40bf0/ijms-25-09588-g001.jpg

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