Hansen Eric, Janson Christopher, Romanova Liudmila, Lam Cornelius
Department of Neurosurgery, Minneapolis Veterans Administration Health Care System, Minneapolis, United States.
Department of Internal Medicine and Neurology, Wright State University, Beavercreek, United States.
Basic Clin Neurosci. 2024 Mar-Apr;15(2):221-232. doi: 10.32598/bcn.2022.3089.1. Epub 2024 Mar 1.
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.
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.
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.
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.
软脑膜-蛛网膜是脑脊液清除的关键组成部分。它覆盖并内陷至脑实质,生理功能衰竭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中的作用,并确定水通量和溶质转运是否受这些脑实质内细胞的影响。
使用永生化大鼠蛛网膜细胞系接种4周龄大鼠的300μm脑片。在脑实质内生长7-10天后进行液体和示踪剂转运分析。使用扩散室实验对蛛网膜脑片模型的发育进行表征,以计算渗透率、扩散系数和通量。
标记的大鼠蛛网膜细胞可在长达10天的时间内轻易穿透器官型培养物。在扩散室中放置3小时后,观察到穿过蛛网膜浸润脑片的染料和水通量显著降低。与不含蛛网膜细胞的脑片相比,含有蛛网膜细胞的全脑片渗透率降低。相比之下,当分子量从40 kDa增加到70 kDa时,所有脑片上的右旋糖酐通量均显著降低。
示踪剂和小分子研究表明,蛛网膜细胞的存在显著影响水在脑实质中的移动。尺寸差异实验表明,溶质渗透率在40 kDa至70 kDa之间发生了显著变化,这是血脑屏障定义的一个重要标志。我们开发了一种蛛网膜器官型模型,揭示了它们改变渗透率和转运的能力。