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Convective influx/glymphatic system: tracers injected into the CSF enter and leave the brain along separate periarterial basement membrane pathways

机译:对流涌入/淋巴系统:注入CSF的示踪剂沿着独立的动脉周围基底膜途径进入和离开大脑

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摘要

Tracers injected into CSF pass into the brain alongside arteries and out again. This has been recently termed the “glymphatic system” that proposes tracers enter the brain along periarterial “spaces” and leave the brain along the walls of veins. The object of the present study is to test the hypothesis that: (1) tracers from the CSF enter the cerebral cortex along pial-glial basement membranes as there are no perivascular “spaces” around cortical arteries, (2) tracers leave the brain along smooth muscle cell basement membranes that form the Intramural Peri-Arterial Drainage (IPAD) pathways for the elimination of interstitial fluid and solutes from the brain. 2 μL of 100 μM soluble, fluorescent fixable amyloid β (Aβ) were injected into the CSF of the cisterna magna of 6–10 and 24–30 month-old male mice and their brains were examined 5 and 30 min later. At 5 min, immunocytochemistry and confocal microscopy revealed Aβ on the outer aspects of cortical arteries colocalized with α-2 laminin in the pial-glial basement membranes. At 30 min, Aβ was colocalised with collagen IV in smooth muscle cell basement membranes in the walls of cortical arteries corresponding to the IPAD pathways. No evidence for drainage along the walls of veins was found. Measurements of the depth of penetration of tracer were taken from 11 regions of the brain. Maximum depths of penetration of tracer into the brain were achieved in the pons and caudoputamen. Conclusions drawn from the present study are that tracers injected into the CSF enter and leave the brain along separate periarterial basement membrane pathways. The exit route is along IPAD pathways in which Aβ accumulates in cerebral amyloid angiopathy (CAA) in Alzheimer’s disease. Results from this study suggest that CSF may be a suitable route for delivery of therapies for neurological diseases, including CAA.Electronic supplementary materialThe online version of this article (10.1007/s00401-018-1862-7) contains supplementary material, which is available to authorized users.
机译:注射到脑脊液中的示踪剂与动脉一起进入大脑,然后再次流出。最近,这被称为“淋巴系统”,该系统建议示踪剂沿动脉周围的“空间”进入大脑,然后沿静脉壁离开大脑。本研究的目的是检验以下假设:(1)示踪剂从CSF沿着胶质细胞基底膜进入大脑皮层,因为在皮质动脉周围没有血管周围的“空间”,(2)示踪剂沿大脑离开平滑肌细胞基底膜形成壁间动脉内引流(IPAD)通路,可消除大脑中的组织液和溶质。将2μL的100μM可溶性,荧光固定的淀粉样蛋白β(Aβ)注入6-10和24-30个月大的雄性小鼠的大水罐的CSF中,并在5和30分钟后检查其大脑。在第5分钟时,免疫细胞化学和共聚焦显微镜检查显示,在皮层和胶质细胞基底膜中,与β-2层粘连蛋白共定位的皮质动脉外部存在Aβ。在30分钟时,Aβ与IV型胶原蛋白共定位在与IPAD通路相对应的皮质动脉壁平滑肌细胞基底膜中。没有发现沿静脉壁引流的证据。从大脑的11个区域进行了示踪剂渗透深度的测量。在脑桥和caudoputamen中实现了示踪剂渗透到大脑的最大深度。从本研究得出的结论是,注入CSF的示踪剂沿着分开的动脉周围基底膜途径进入和离开大脑。退出途径沿IPAD途径,其中Aβ在阿尔茨海默氏病的脑淀粉样血管病(CAA)中积累。这项研究的结果表明,脑脊液可能是神经疾病包括CAA的合适治疗途径。电子补充材料本文的在线版本(10.1007 / s00401-018-1862-7)包含补充材料,可用于授权用户。

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