实质蛛网膜对脑液运输的影响

Eric Hansen, Christopher Janson, Liudmila Romanova, Cornelius Lam
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摘要

简介蛛网膜是清除脑脊液的重要组成部分。蛛网膜覆盖并侵入脑实质,生理性失效会导致脑积水和脑水肿。本研究的目的是描述蛛网膜在脑实质内的作用,并确定这些脑实质内细胞是否会影响水通量和溶质运输:方法:用永生化的大鼠蛛网膜细胞系为 4 周龄大鼠的 300μm 器官型大鼠脑切片播种。经过7-10天的实质内生长期后,进行了流体和示踪剂运输分析。利用扩散室实验来计算渗透性、扩散系数和通量,从而确定蛛网膜脑切片模型的发展特征:结果:标记的大鼠蛛网膜细胞很容易穿透器官型培养物长达 10 天。在扩散室中观察 3 小时后,蛛网膜浸渍脑片上的染料和水通量明显减少。与不含蛛网膜细胞的脑片相比,含蛛网膜细胞的整个脑片的渗透性降低。相比之下,当分子量从 40 kDa 增加到 70 kDa 时,葡聚糖在所有切片上的渗透性都会显著降低:示踪剂和小分子研究表明,蛛网膜细胞的存在对水在脑实质中的流动有显著影响。大小差异实验表明,溶质的渗透性在 40 至 70 kDa 之间发生了很大变化,这是血液-脑脊液屏障定义的一个重要标志。我们开发了一种蛛网膜有机模型,揭示了它们改变渗透性和运输的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Parenchymal Arachnoid on Brain Fluid Transport.

Introduction: The pia-arachnoid is a critical component of cerebrospinal fluid removal. It covers and invaginates into the brain parenchyma, and physiologic failure results in hydrocephalus and cerebral edema. The purpose of this study was to characterize the role of arachnoid within brain parenchyma and determine if water flux and solute transport are affected by these intra-parenchymal cells.

Methods: An immortalized arachnoid rat cell line was used to seed 300-μm organotypic rat brain slices of 4-week-old rats. Fluid and tracer transport analyses were conducted following a 7-10 day intraparenchymal growth period. The development of an arachnoid brain slice model was characterized using diffusion chamber experiments to calculate permeability, diffusion coefficient, and flux.

Results: Labeled rat arachnoid cells readily penetrated organotypic cultures for up to 10 days. A significant reduction of dye and water flux across arachnoid-impregnated brain slices was observed after 3 hours in the diffusion chamber. Permeability decreased in whole brain slices containing arachnoid cells compared to slices without arachnoid cells. In comparison, a significant reduction of dextran across all slices occurred when molecular weights increased from 40 to 70 kDa.

Conclusion: Tracer and small molecule studies show that arachnoid cells' presence significantly impacts water's movement through brain parenchyma. Size differential experiments indicate that the permeability of solute changed substantially between 40 and 70 kDa, an essential marker of blood-CSF barrier definition. We have developed an arachnoid organotypic model that reveals their ability to alter permeability and transport.

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