Suppr超能文献

使用384柱板上的3D培养神经干细胞进行化合物神经毒性的高通量筛选

High-Throughput Screening of Compound Neurotoxicity Using 3D-Cultured Neural Stem Cells on a 384-Pillar Plate.

作者信息

Kang Soo-Yeon, Joshi Pranav, Lee Moo-Yeal

机构信息

Department of Chemical and Biomedical Engineering, Cleveland State University, Cleveland, Ohio.

出版信息

Curr Protoc. 2021 Apr;1(4):e107. doi: 10.1002/cpz1.107.

Abstract

Assessing the neurotoxicity of test chemicals has typically been performed using two-dimensionally (2D)-cultured neuronal cell monolayers and animal models. The in vitro 2D cell models are simple and straightforward compared to animal models, which have the disadvantage of being relatively low throughput, expensive, and time consuming. Despite their extensive use in this area of neurotoxicology research, both models often do not accurately recapitulate human outcomes. To bridge this gap and attempt to better replicate what happens in vivo, three-dimensionally (3D) cultured neural stem cells (NSCs) encapsulated in hydrogels on a 384-pillar plate have been developed via miniature 3D bioprinting. This technology allows users to print NSCs on a pillar plate for rapid 3D cell culture as well as high-throughput compound screening. For this, the 384-pillar plate with bioprinted NSCs is sandwiched with a standard 384-well plate with growth medium for 3D culture, allowing researchers to expose the cells to test compounds and stain them with various fluorescent dyes for a suite of high-content imaging assays, including assays for DNA damage, mitochondrial impairment, cell membrane integrity, intracellular glutathione levels, and apoptosis. After acquiring cell images from an automated fluorescence microscope and extracting fluorescence intensities, researchers can obtain the IC value of each compound to evaluate critical parameters in neurotoxicity. Here, we provide a detailed description of protocols for cell printing on a 384-pillar plate, 3D NSC culture, compound testing, 3D cell staining, and image acquisition and analysis, which altogether will allow researchers to investigate mechanisms of compound neurotoxicity with 3D-cultured NSCs in a high-throughput manner. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Three-dimensional neural stem cell culture on a 384-pillar plate Basic Protocol 2: Compound treatment and cell staining Basic Protocol 3: Image acquisition, processing, and data analysis.

摘要

评估受试化学品的神经毒性通常使用二维(2D)培养的神经元细胞单层和动物模型。与动物模型相比,体外2D细胞模型简单直接,而动物模型具有通量相对较低、成本高和耗时的缺点。尽管它们在神经毒理学研究领域被广泛使用,但这两种模型往往都不能准确重现人体实验结果。为了弥补这一差距并尝试更好地复制体内发生的情况,通过微型3D生物打印技术,开发出了封装在水凝胶中的三维(3D)培养神经干细胞(NSC),并将其置于384柱板上。这项技术允许用户在柱板上打印神经干细胞,以进行快速3D细胞培养以及高通量化合物筛选。为此,将印有神经干细胞的384柱板与装有生长培养基的标准384孔板夹在一起进行3D培养,使研究人员能够将细胞暴露于受试化合物中,并用各种荧光染料对其进行染色,以进行一系列高内涵成像分析,包括DNA损伤、线粒体损伤、细胞膜完整性、细胞内谷胱甘肽水平和细胞凋亡分析。从自动荧光显微镜获取细胞图像并提取荧光强度后,研究人员可以获得每种化合物的半数抑制浓度(IC)值,以评估神经毒性的关键参数。在此,我们详细描述了在384柱板上进行细胞打印、3D神经干细胞培养、化合物测试、3D细胞染色以及图像采集和分析的方案,这些方案将使研究人员能够以高通量方式研究3D培养的神经干细胞的化合物神经毒性机制。© 2021威利期刊有限责任公司。基本方案1:在384柱板上进行三维神经干细胞培养 基本方案2:化合物处理和细胞染色 基本方案3:图像采集、处理和数据分析。

相似文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验