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建立一种永生化小鼠脑微血管内皮细胞系作为体外血脑屏障模型。

Generation of an immortalized murine brain microvascular endothelial cell line as an in vitro blood brain barrier model.

作者信息

Burek Malgorzata, Salvador Ellaine, Förster Carola Y

机构信息

Klinik und Poliklinik für Anästhesiologie, University of Wurzburg.

出版信息

J Vis Exp. 2012 Aug 29(66):e4022. doi: 10.3791/4022.

Abstract

Epithelial and endothelial cells (EC) are building paracellular barriers which protect the tissue from the external and internal environment. The blood-brain barrier (BBB) consisting of EC, astrocyte end-feet, pericytes and the basal membrane is responsible for the protection and homeostasis of the brain parenchyma. In vitro BBB models are common tools to study the structure and function of the BBB at the cellular level. A considerable number of different in vitro BBB models have been established for research in different laboratories to date. Usually, the cells are obtained from bovine, porcine, rat or mouse brain tissue (discussed in detail in the review by Wilhelm et al.). Human tissue samples are available only in a restricted number of laboratories or companies. While primary cell preparations are time consuming and the EC cultures can differ from batch to batch, the establishment of immortalized EC lines is the focus of scientific interest. Here, we present a method for establishing an immortalized brain microvascular EC line from neonatal mouse brain. We describe the procedure step-by-step listing the reagents and solutions used. The method established by our lab allows the isolation of a homogenous immortalized endothelial cell line within four to five weeks. The brain microvascular endothelial cell lines termed cEND (from cerebral cortex) and cerebEND (from cerebellar cortex), were isolated according to this procedure in the Förster laboratory and have been effectively used for explanation of different physiological and pathological processes at the BBB. Using cEND and cerebEND we have demonstrated that these cells respond to glucocorticoid- and estrogen-treatment as well as to pro-infammatory mediators, such as TNFalpha. Moreover, we have studied the pathology of multiple sclerosis and hypoxia on the EC-level. The cEND and cerebEND lines can be considered as a good tool for studying the structure and function of the BBB, cellular responses of ECs to different stimuli or interaction of the EC with lymphocytes or cancer cells.

摘要

上皮细胞和内皮细胞构建了细胞旁屏障,保护组织免受外部和内部环境的影响。由内皮细胞、星形胶质细胞终足、周细胞和基底膜组成的血脑屏障负责保护脑实质并维持其稳态。体外血脑屏障模型是在细胞水平研究血脑屏障结构和功能的常用工具。迄今为止,不同实验室已建立了大量不同的体外血脑屏障模型用于研究。通常,细胞取自牛、猪、大鼠或小鼠的脑组织(Wilhelm等人的综述中有详细讨论)。人类组织样本仅在少数实验室或公司中可得。虽然原代细胞制备耗时且内皮细胞培养批次间可能存在差异,但永生化内皮细胞系的建立是科学研究的重点。在此,我们介绍一种从新生小鼠脑建立永生化脑微血管内皮细胞系的方法。我们逐步描述该过程,列出所用的试剂和溶液。我们实验室建立的方法可在四到五周内分离出同质的永生化内皮细胞系。在Förster实验室,按照此程序分离出了称为cEND(来自大脑皮层)和cerebEND(来自小脑皮层)的脑微血管内皮细胞系,并已有效地用于解释血脑屏障处不同的生理和病理过程。使用cEND和cerebEND,我们已证明这些细胞对糖皮质激素和雌激素处理以及促炎介质(如TNFα)有反应。此外,我们在细胞水平上研究了多发性硬化症和缺氧的病理学。cEND和cerebEND细胞系可被视为研究血脑屏障结构和功能、内皮细胞对不同刺激的细胞反应或内皮细胞与淋巴细胞或癌细胞相互作用的良好工具。

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