生成三维动脉粥样硬化芯片模型的方案,用于研究动脉粥样硬化中内皮-巨噬细胞串扰。

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
Katie M L Hanford, Kim E Dzobo, Miranda Versloot, Jorge Peter, Jeffrey Kroon
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引用次数: 0

摘要

内皮是血管健康的看门人,其功能障碍是驱动动脉粥样硬化的关键。在这里,我们提出了一种方案,以模拟双通道灌注系统为基础,在动脉粥样硬化过程中复制内皮-巨噬细胞串扰,称为“芯片上动脉粥样硬化”模型。我们描述了一个模型,用于研究人类主动脉内皮细胞和巨噬细胞在动脉粥样硬化过程中的内皮-巨噬细胞相互作用,使用qPCR和分泌组分析,荧光显微镜和流式细胞术。该方案可适用于更复杂的斑块微环境或其他疾病情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocol to generate a 3D atherogenesis-on-chip model for studying endothelial-macrophage crosstalk in atherogenesis.

The endothelium is the gatekeeper of vessel health, and its dysfunction is pivotal in driving atherogenesis. Here, we present a protocol to replicate endothelial-macrophage crosstalk during atherogenesis, called the "atherogenesis-on-chip" model, based on the Emulate dual-channel perfusion system. We describe a model for studying endothelial-macrophage interactions during atherogenesis in human aortic endothelial cells and human macrophages using qPCR and secretome analysis, fluorescence microscopy, and flow cytometry. This protocol could be adapted toward more complex plaque microenvironment or other disease settings.

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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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