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一种用于体外研究血脑屏障的更简便、可重复且能大规模生产的方法。

An easier, reproducible, and mass-production method to study the blood-brain barrier in vitro.

作者信息

Dehouck M P, Méresse S, Delorme P, Fruchart J C, Cecchelli R

机构信息

SERLIA, INSERM U. 325, Institut Pasteur, Lille, France.

出版信息

J Neurochem. 1990 May;54(5):1798-801. doi: 10.1111/j.1471-4159.1990.tb01236.x.

Abstract

To provide an "in vitro" system for studying brain capillary function, we have developed a process of coculture that closely mimics the "in vivo" situation by culturing brain capillary endothelial cells on one side of a filter and astrocytes on the other. Under these conditions, endothelial cells retain all the endothelial cell markers and the characteristics of the blood-brain barrier, including tight junctions and gamma-glutamyl transpeptidase activity. The average electric resistance for the monolayers was 661 omega cm2. The system is impermeable to inulin and sucrose but allows the transport of leucine. Arabinose treatment increases transcellular transport flux by 70%. The relative ease with which such monolayers can be produced in large quantities would facilitate the "in vitro" study of brain capillary functions.

摘要

为了提供一个用于研究脑毛细血管功能的“体外”系统,我们开发了一种共培养方法,通过在滤器一侧培养脑毛细血管内皮细胞,另一侧培养星形胶质细胞,紧密模拟“体内”情况。在这些条件下,内皮细胞保留所有内皮细胞标志物以及血脑屏障的特征,包括紧密连接和γ-谷氨酰转肽酶活性。单层细胞的平均电阻为661Ω·cm²。该系统对菊粉和蔗糖不可渗透,但允许亮氨酸转运。阿拉伯糖处理使跨细胞转运通量增加70%。如此大量生产这种单层细胞的相对简便性将有助于脑毛细血管功能的“体外”研究。

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