Mehrotra Trisha, Shi Xiaodi, Merlin Didier
Institute for Biomedical Sciences, Digestive Diseases Research Group, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, GA, USA.
Atlanta Veterans Affairs Medical Center, Decatur, GA, USA.
Bio Protoc. 2024 Mar 5;14(5):e4950. doi: 10.21769/BioProtoc.4950.
Here, we describe immunofluorescent (IF) staining assay of 3D cell culture colonoids isolated from mice colon as described previously. Primary cultures developed from isolated colonic stem cells are called colonoids. Immunofluorescence can be used to analyze the distribution of proteins, glycans, and small molecules-both biological and non-biological ones. Four-day-old colonoid cell cultures grown on Lab-Tek 8-well plate are fixed by paraformaldehyde. Fixed colonoids are then subjected to antigen retrieval and blocking followed by incubation with primary antibody. A corresponding secondary antibody tagged with desired fluorescence is used to visualize primary antibody-marked protein. Counter staining to stain actin filaments and nucleus to assess cell structure and DNA in nucleus is performed by choosing the other two contrasting fluorescences. IF staining of colonoids can be utilized to visualize molecular markers of cell behavior. This technique can be used for translation research by isolating colonoids from colitis patients' colons, monitoring the biomarkers, and customizing their treatments. Key features • Analysis of molecular markers of cell behavior. • Protocol to visualize proteins in 3D cell culture. • This protocol requires colonoids isolated from mice colon grown on matrigel support. • Protocol requires at least eight days to complete.
在此,我们描述了如前所述对从小鼠结肠分离的三维细胞培养类结肠进行免疫荧光(IF)染色分析的方法。从分离的结肠干细胞中培养的原代培养物称为类结肠。免疫荧光可用于分析蛋白质、聚糖以及生物和非生物小分子的分布。在Lab-Tek 8孔板上培养4天的类结肠细胞培养物用多聚甲醛固定。然后对固定的类结肠进行抗原修复和封闭,随后与一抗孵育。使用标记有所需荧光的相应二抗来可视化一抗标记的蛋白质。通过选择另外两种对比荧光对肌动蛋白丝和细胞核进行复染,以评估细胞结构和细胞核中的DNA。类结肠的IF染色可用于可视化细胞行为的分子标记。通过从结肠炎患者的结肠中分离类结肠、监测生物标志物并定制其治疗方案,该技术可用于转化研究。关键特性 • 分析细胞行为的分子标记。 • 在三维细胞培养中可视化蛋白质的方案。 • 该方案需要在基质胶支持物上培养从小鼠结肠分离的类结肠。 • 该方案至少需要八天才能完成。