Troili Fernanda, Cipollini Virginia, Moci Marco, Morena Emanuele, Palotai Miklos, Rinaldi Virginia, Romano Carmela, Ristori Giovanni, Giubilei Franco, Salvetti Marco, Orzi Francesco, Guttmann Charles R G, Cavallari Michele
Department of Neurosciences Mental Health and Sensory Organs, Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy.
Department of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana", Neuroscience Section, University of Salerno, Baronissi, Italy.
Front Neuroanat. 2020 Apr 16;14:17. doi: 10.3389/fnana.2020.00017. eCollection 2020.
Most neurological disorders seemingly have heterogenous pathogenesis, with overlapping contribution of neuronal, immune and vascular mechanisms of brain injury. The perivascular space in the brain represents a crossroad where those mechanisms interact, as well as a key anatomical component of the recently discovered glymphatic pathway, which is considered to play a crucial role in the clearance of brain waste linked to neurodegenerative diseases. The pathological interplay between neuronal, immune and vascular factors can create an environment that promotes self-perpetration of mechanisms of brain injury across different neurological diseases, including those that are primarily thought of as neurodegenerative, neuroinflammatory or cerebrovascular. Changes of the perivascular space can be monitored in humans using magnetic resonance imaging (MRI). In the context of glymphatic clearance, MRI-visible enlarged perivascular spaces (EPVS) are considered to reflect glymphatic stasis secondary to the perivascular accumulation of brain debris, although they may also represent an adaptive mechanism of the glymphatic system to clear them. EPVS are also established correlates of dementia and cerebral small vessel disease (SVD) and are considered to reflect brain inflammatory activity. In this review, we describe the "perivascular unit" as a key anatomical and functional substrate for the interaction between neuronal, immune and vascular mechanisms of brain injury, which are shared across different neurological diseases. We will describe the main anatomical, physiological and pathological features of the perivascular unit, highlight potential substrates for the interplay between different noxae and summarize MRI studies of EPVS in cerebrovascular, neuroinflammatory and neurodegenerative disorders.
大多数神经系统疾病似乎具有异质性发病机制,脑损伤的神经元、免疫和血管机制均有重叠作用。脑内的血管周围间隙是这些机制相互作用的交汇点,也是最近发现的类淋巴途径的关键解剖组成部分,该途径被认为在清除与神经退行性疾病相关的脑内废物方面起着至关重要的作用。神经元、免疫和血管因素之间的病理相互作用可营造一种环境,促进不同神经系统疾病(包括那些主要被认为是神经退行性、神经炎症性或脑血管性疾病)的脑损伤机制自我持续。血管周围间隙的变化可通过磁共振成像(MRI)在人体中进行监测。在类淋巴清除的背景下,MRI可见的血管周围间隙扩大(EPVS)被认为反映了脑碎片在血管周围积聚继发的类淋巴淤滞,尽管它们也可能代表类淋巴系统清除这些碎片的一种适应性机制。EPVS也是痴呆和脑小血管病(SVD)的确立相关指标,被认为反映了脑内炎症活动。在本综述中,我们将“血管周围单元”描述为脑损伤的神经元、免疫和血管机制之间相互作用的关键解剖和功能基础,这些机制在不同神经系统疾病中是共有的。我们将描述血管周围单元的主要解剖、生理和病理特征,强调不同损伤因素之间相互作用的潜在基础,并总结脑血管、神经炎症和神经退行性疾病中EPVS的MRI研究。