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小鼠胚胎成纤维细胞培养与刺激

Mouse Embryonic Fibroblast Cell Culture and Stimulation.

作者信息

Qiu Lian-Qun, Lai Wi S, Stumpo Deborah J, Blackshear Perry J

机构信息

Post-transcriptional Gene Expression Group, Signal Transduction Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, USA.

出版信息

Bio Protoc. 2016 Jul 5;6(13). doi: 10.21769/BioProtoc.1859.

Abstract

Culture of mouse embryonic fibroblast (MEF) cells represents a powerful system to test gene function due to their easy accessibility, rapid growth rates, and the possibility of a large number of experiments. Fibroblasts are a group of heterogeneous resident cells of mesenchymal origin that have various locations, diverse appearances and distinctive activities. Because of their ubiquitous distribution as tissue cells, these cells are poised to respond to factors released by newly activated innate immune cells, thus becoming a useful tool to study inflammation and immunity. Here, we describe procedures for mouse embryonic fibroblast cell isolation, primary culture, and stimulation. Specifically, we have optimized a step of serum starvation prior to stimulation. This step is necessary to maintain the quiescent status of these cells before they are exposed to pro-inflammatory stimuli for optimal responses. As shown in our previous studies, these mouse fibroblasts do not express , , or mRNAs at levels readily detectable by routine northern blotting techniques (Lai WS ., 2006).

摘要

小鼠胚胎成纤维细胞(MEF)培养是一个强大的系统,可用于测试基因功能,这是因为它们易于获取、生长速度快,并且能够进行大量实验。成纤维细胞是一组间充质来源的异质驻留细胞,具有不同的位置、多样的外观和独特的活性。由于它们作为组织细胞广泛分布,这些细胞易于对新激活的先天免疫细胞释放的因子作出反应,从而成为研究炎症和免疫的有用工具。在此,我们描述了小鼠胚胎成纤维细胞分离、原代培养和刺激的程序。具体而言,我们优化了刺激前血清饥饿的步骤。此步骤对于在这些细胞暴露于促炎刺激以获得最佳反应之前维持其静止状态是必要的。如我们先前的研究所示,这些小鼠成纤维细胞不表达、或mRNA,其水平用常规Northern印迹技术难以轻易检测到(Lai WS.,2006)。

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