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血脑屏障的体外模型。

In vitro models of the blood-brain barrier.

作者信息

Czupalla Cathrin J, Liebner Stefan, Devraj Kavi

机构信息

Institute of Neurology (Edinger Institute), Johann Wolfgang Goethe-University Frankfurt Medical School, Frankfurt, Germany.

出版信息

Methods Mol Biol. 2014;1135:415-37. doi: 10.1007/978-1-4939-0320-7_34.

Abstract

The blood-brain barrier (BBB) proper is composed of endothelial cells (ECs) of the cerebral microvasculature, which are interconnected by tight junctions (TJs) that in turn form a physical barrier restricting paracellular flux. Tight control of vascular permeability is essential for the homeostasis and functionality of the central nervous system (CNS). In vitro BBB models have been in use for decades and have been of great benefit in the process of investigating and understanding the cellular and molecular mechanisms underlying BBB establishment. BBB integrity changes can be addressed in vitro by determining cell monolayer permeability (Pe) to different solutes and measuring trans-endothelial electrical resistance (TEER).This chapter describes procedures that can be utilized for both freshly isolated mouse brain microvascular ECs (MBMECs) and murine or human brain EC lines (bEnd5 or hCMEC/D3), cultivated either as a single monolayer or in cocultivation with primary mouse astrocytes (ACs). It starts with detailed information on how to perform transwell cell culture, including coating of inserts and seeding of the ECs and ACs. Moreover, it encompasses instructions for electrical assessment of the in vitro BBB using the more recent cellZscope(®) device, which was traditionally performed with chopstick electrodes of voltohmmeter type (EVOM). From continuous impedance measurements, the cellZscope(®) device provides TEER (paracellular resistance) and cell membrane capacitance (Ccl-transcellular resistance), two independent measures of monolayer integrity. Additionally, this chapter provides guidance through subsequent experiments such as permeability analysis (Pe, flux), expression analysis (qRT-PCR and Western blotting), and localization analysis of BBB junction proteins (immunocytochemistry) using the same inserts subjected earlier to impedance analysis.As numerous diseases are associated with BBB breakdown, researchers aim to continuously improve and refine in vitro BBB models to mimic in vivo conditions as closely as possible. This chapter summarizes protocols with the intention to provide a collection of BBB in vitro assays that generate reproducible results not only with primary brain ECs but also with EC lines to open up the field for a broader spectrum of researchers who intend to investigate the BBB in vitro particularly aiming at therapeutic aspects.

摘要

血脑屏障(BBB)本身由脑微血管的内皮细胞(ECs)组成,这些内皮细胞通过紧密连接(TJs)相互连接,紧密连接进而形成一个限制细胞旁通量的物理屏障。严格控制血管通透性对于中枢神经系统(CNS)的稳态和功能至关重要。体外血脑屏障模型已经使用了数十年,在研究和理解血脑屏障形成的细胞和分子机制过程中发挥了巨大作用。血脑屏障完整性的变化可以通过测定细胞单层对不同溶质的通透性(Pe)和测量跨内皮电阻(TEER)在体外进行研究。本章介绍了可用于新鲜分离的小鼠脑微血管内皮细胞(MBMECs)以及小鼠或人脑内皮细胞系(bEnd5或hCMEC/D3)的实验步骤,这些细胞可以单层培养,也可以与原代小鼠星形胶质细胞(ACs)共培养。本章首先详细介绍了如何进行Transwell细胞培养,包括小室包被以及内皮细胞和星形胶质细胞的接种。此外,还包括使用更新的cellZscope(®)设备对体外血脑屏障进行电学评估的说明,传统上这是使用伏特计型筷子电极(EVOM)进行的。通过连续阻抗测量,cellZscope(®)设备可提供TEER(细胞旁电阻)和细胞膜电容(Ccl - 跨细胞电阻),这是单层完整性的两个独立测量指标。此外,本章还通过后续实验提供指导,例如使用先前进行过阻抗分析的相同小室进行通透性分析(Pe、通量)、表达分析(qRT - PCR和蛋白质免疫印迹)以及血脑屏障连接蛋白的定位分析(免疫细胞化学)。由于许多疾病都与血脑屏障破坏有关,研究人员旨在不断改进和完善体外血脑屏障模型,以尽可能逼真地模拟体内情况。本章总结了相关实验方案,旨在提供一系列体外血脑屏障检测方法,这些方法不仅能在原代脑内皮细胞中,也能在细胞系中产生可重复的结果,从而为更广泛的研究人员开辟研究领域,这些研究人员尤其希望从治疗角度对体外血脑屏障进行研究。

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