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超越屏障功能:周细胞在神经炎症稳态和调控中的作用。

Beyond barrier functions: Roles of pericytes in homeostasis and regulation of neuroinflammation.

机构信息

Department of Clinical Neurosciences, Hotchkiss Brain institute, University of Calgary, Calgary, AB, Canada.

出版信息

J Neurosci Res. 2020 Dec;98(12):2390-2405. doi: 10.1002/jnr.24715. Epub 2020 Aug 20.

DOI:10.1002/jnr.24715
PMID:32815569
Abstract

Pericytes are contractile cells that extend along the vasculature to mediate key homeostatic functions of endothelial barriers within the body. In the central nervous system (CNS), pericytes are important contributors to the structure and function of the neurovascular unit, which includes endothelial cells, astrocytes and neurons. The understanding of pericytes has been marred by an inability to accurately distinguish pericytes from other stromal cells with similar expression of identifying markers. Evidence is now growing in favor of pericytes being actively involved in both CNS homeostasis and pathology of neurological diseases, including multiple sclerosis, spinal cord injury, and Alzheimer's disease among others. In this review, we discuss the current understanding on the characterization of pericytes, their roles in maintaining the integrity of the blood-brain barrier, and their contributions to neuroinflammation and neurorepair. Owing to its plethora of surface receptors, pericytes respond to inflammatory mediators such as CCL2 (monocyte chemoattractant protein-1) and tumor necrosis factor-α, in turn secreting CCL2, nitric oxide, and several cytokines. Pericytes can therefore act as promoters of both the innate and adaptive arms of the immune system. Much like professional phagocytes, pericytes also have the ability to clear up cellular debris and macromolecular plaques. Moreover, pericytes promote the activities of CNS glia, including in maturation of oligodendrocyte lineage cells for myelination. Conversely, pericytes can impair regenerative processes by contributing to scar formation. A better characterization of CNS pericytes and their functions would bode well for therapeutics aimed at alleviating their undesirable properties and enhancing their benefits.

摘要

周细胞是沿血管延伸的收缩细胞,可介导体内血管内皮屏障的关键稳态功能。在中枢神经系统 (CNS) 中,周细胞是神经血管单元结构和功能的重要贡献者,神经血管单元包括内皮细胞、星形胶质细胞和神经元。对周细胞的理解一直受到无法准确区分周细胞与具有相似鉴定标记表达的其他基质细胞的阻碍。现在有越来越多的证据表明,周细胞积极参与中枢神经系统的稳态和神经疾病的病理学,包括多发性硬化症、脊髓损伤和阿尔茨海默病等。在这篇综述中,我们讨论了目前对周细胞特征的理解,它们在维持血脑屏障完整性中的作用,以及它们对神经炎症和神经修复的贡献。由于其丰富的表面受体,周细胞对趋化因子 CCL2(单核细胞趋化蛋白-1)和肿瘤坏死因子-α 等炎症介质作出反应,反过来分泌 CCL2、一氧化氮和几种细胞因子。因此,周细胞可以作为先天和适应性免疫系统的促进剂。与专业吞噬细胞一样,周细胞还具有清除细胞碎片和大分子斑块的能力。此外,周细胞促进中枢神经系统神经胶质细胞的活动,包括少突胶质细胞谱系细胞的成熟以进行髓鞘形成。相反,周细胞通过促进瘢痕形成来损害再生过程。更好地描述中枢神经系统周细胞及其功能将有助于针对减轻其不良特性和增强其益处的治疗方法。

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