首页> 外文期刊>Annals of Biomedical Engineering: The Journal of the Biomedical Engineering Society >Development of an In Vitro 3D Brain Tissue Model Mimicking In Vivo-Like Pro-inflammatory and Pro-oxidative Responses
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Development of an In Vitro 3D Brain Tissue Model Mimicking In Vivo-Like Pro-inflammatory and Pro-oxidative Responses

机译:体外三维脑组织模型的发展仿生型促炎和促氧化反应

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To analyze complex inflammatory responses in an in vitro system, we constructed a new 3D in vitro brain tissue model that exhibits in vivo-like tissue responses (e.g. immune cell phenotypes, and molecular response) to inflammatory stimuli. Finite element modeling of oxygen diffusion and cellular oxygen consumption predicted the oxygen profile within 3D structures, consisting of Type I collagen hydrogel embedded with murine microglia. Viability and cytotoxicity analyses supported the mathematical analysis, determining optimal cell growth conditions for 3D construct development. Real-time RT-PCR and ELISA demonstrated significant up-regulation of pro-inflammatory mediators, such as TNF-alpha, MCP-1, IL-6 and IL-1 beta, in lipopolysaccharide (LPS)-stimulated in vitro cell culture (2D and 3D) and in vivo mouse model systems. Interestingly, levels of inflammatory responses from the in vitro 3D model system were more similar to in vivo than in vitro 2D. Additionally, in situ dihydroethidium (DHE) assay and immunofluorescence staining revealed that levels of LPS-stimulated reactive oxygen species (ROS) generation and microglial activation from in vitro 3D model system were closer to in vivo than in vitro 2D. These results demonstrated that an in vitro 3D model provides more physiologically relevant pro-oxidative and pro-inflammatory environments in brain than an in vitro 2D model.
机译:为了在体外系统中分析复杂的炎症反应,我们构建了一种新的3D体外脑组织模型,其具有炎性刺激的体内组织反应(例如免疫细胞表型和分子反应)。氧扩散的有限元建模和蜂窝氧消耗预测了3D结构内的氧气轮廓,由嵌入鼠髓微胶质的I型胶原水凝胶组成。活力和细胞毒性分析支持数学分析,确定3D构建开发的最佳细胞生长条件。实时RT-PCR和ELISA证明了促炎介质的显着上调,例如TNF-α,MCP-1,IL-6和IL-1β,在脂多糖(LPS)的体外细胞培养中( 2D和3D)和体内鼠标模型系统。有趣的是,体外3D模型系统的炎症反应的水平比体内比体内更相似。另外,原位二羟基羟乙酰胺(DHE)测定和免疫荧光染色表明,来自体外3D模型系统的LPS刺激的活性氧物质(ROS)产生和微胶质激活比体内比体内2D更接近体内。这些结果表明,体外3D模型在大脑中提供了比体外2D模型更具生理相关的亲氧化和促炎环境。

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