Rothschild Daniel E, Srinivasan Tara, Aponte-Santiago Linette A, Shen Xiling, Allen Irving C
Department of Biomedical Sciences and Pathobiology, Virginia Maryland College of Veterinary Medicine, Virginia Tech.
Department of Biomedical Engineering, Cornell University.
J Vis Exp. 2016 May 18(111):54033. doi: 10.3791/54033.
Primary intestinal organoids are a valuable model system that has the potential to significantly impact the field of mucosal immunology. However, the complexities of the organoid growth characteristics carry significant caveats for the investigator. Specifically, the growth patterns of each individual organoid are highly variable and create a heterogeneous population of epithelial cells in culture. With such caveats, common tissue culture practices cannot be simply applied to the organoid system due to the complexity of the cellular structure. Counting and plating based solely on cell number, which is common for individually separated cells, such as cell lines, is not a reliable method for organoids unless some normalization technique is applied. Normalizing to total protein content is made complex due to the resident protein matrix. These characteristics in terms of cell number, shape and cell type should be taken into consideration when evaluating secreted contents from the organoid mass. This protocol has been generated to outline a simple procedure to culture and treat small intestinal organoids with microbial pathogens and pathogen associated molecular patterns (PAMPs). It also emphasizes the normalization techniques that should be applied when protein analysis are conducted after such a challenge.
原发性肠道类器官是一种有价值的模型系统,有可能对黏膜免疫学领域产生重大影响。然而,类器官生长特性的复杂性给研究者带来了重大警示。具体而言,每个类器官的生长模式高度可变,在培养中形成了异质性的上皮细胞群体。鉴于这些警示,由于细胞结构的复杂性,常见的组织培养方法不能简单地应用于类器官系统。仅基于细胞数量进行计数和接种,这在单独分离的细胞(如细胞系)中很常见,但对于类器官来说不是一种可靠的方法,除非应用某种归一化技术。由于存在固有蛋白质基质,使归一化至总蛋白质含量变得复杂。在评估类器官群体分泌的成分时,应考虑细胞数量、形状和细胞类型等特征。本方案旨在概述一种用微生物病原体和病原体相关分子模式(PAMPs)培养和处理小肠类器官的简单程序。它还强调了在这种刺激后进行蛋白质分析时应应用的归一化技术。