神经胶质-免疫网络:星形胶质细胞和少突胶质细胞作为健康和疾病中的小胶质协调者。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Verity F T Mitchener, Millie J Thackray, I Lorena Arancibia-Cárcamo
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引用次数: 0

摘要

人们早已确定小胶质细胞是中枢神经系统免疫系统的组成部分。它们的测量和适应性质是大脑发育和维持内稳态以及神经病理表现和进展的关键。然而,随着技术的进步,人们越来越认识到,它们不能孤立地发挥这一作用。以前,大多数研究都集中在小胶质细胞衍生的信号传导上,而很少关注大胶质细胞(星形胶质细胞、少突胶质细胞)的感知和信号传导能力。单细胞转录组学的最新发展已经允许对健康和疾病中的细胞谱进行广泛的分析;这些研究引起了人们对大胶质细胞参与免疫信号通路的能力的关注。这在神经病理学中尤其重要,包括阿尔茨海默病(AD),其中神经胶质细胞(dag)的特定疾病相关谱已经建立。这些变化主要与免疫途径有关,而免疫途径长期以来被认为仅限于免疫细胞,包括细胞因子和趋化因子的产生、抗原呈递和吞噬。越来越多的证据表明,神经胶质细胞应被视为中枢神经系统免疫系统的活性成分,形成一个神经胶质特异性免疫样网络,其中大胶质细胞作为中枢神经系统微环境的传感器,在这个网络中发挥作用,协调中枢神经系统的各种效应/功能。为了深入了解阿尔茨海默病的病理,需要阐明胶质细胞的亲密分子对话。本综述旨在研究大胶质细胞来源的免疫信号及其在健康和疾病中的相关性的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The glia-immune network: Astrocytes and oligodendrocytes as microglial co-ordinators in health and disease.

It has long been established that microglia are integral to the CNS immune system. Their surveying and adaptive nature is key in brain development and maintaining homeostasis as well as in the manifestation and progression of neuropathology. However with advancing technology it is becoming increasingly recognised that they do not serve this role in isolation. Previously most work has focused on microglia-derived signalling, with less attention on the sensing and signalling capacity of macroglia (astrocytes, oligodendrocytes). Recent developments in single-cell transcriptomics have allowed extensive analysis of cell profiles in health and disease; these studies have drawn attention to the capacity of macroglia to also engage in immune signalling pathways. This is particularly relevant in neuropathologies, including in Alzheimer's disease (AD), where specific disease-associated profiles of glia (DAGs) have been established. These changes are predominantly related to immune pathways, which were long considered limited to immune cells, including cytokine and chemokine production, antigen presentation and phagocytosis. There is an increasing body of evidence that glia should be considered as active components of the CNS immune system forming a glia-specific immune-like network, whereby macroglia, acting as sensors of the CNS microenvironment, function within this network to co-ordinate diverse CNS effect(s)/function(s). To gain an in-depth understanding of AD pathology, the intimate molecular dialogue of glia needs to be elucidated. This review aims to examine the evidence for macroglia-derived immune signalling and its relevance in health and disease.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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