Tricoli Lucas, Berry Deborah L, Albanese Chris
Department of Oncology, Lombardi Comprehensive Cancer Center.
Department of Oncology, Georgetown University Medical Center.
J Vis Exp. 2017 Feb 13(120):55279. doi: 10.3791/55279.
Conditionally reprogrammed cells (CRCs) provide a sustainable method for primary cell culture and the ability to develop extensive "living biobanks" of patient derived cell lines. For many types of epithelial cells, various three dimensional (3D) culture approaches have been described that support an improved differentiated state. While CRCs retain their lineage commitment to the tissue from which they are isolated, they fail to express many of the differentiation markers associated with the tissue of origin when grown under normal two dimensional (2D) culture conditions. To enhance the application of patient-derived CRCs for prostate cancer research, a 3D culture format has been defined that enables a rapid (2 weeks total) luminal cell differentiation in both normal and tumor-derived prostate epithelial cells. Herein, a filter insert-based format is described for the culturing and differentiation of both normal and malignant prostate CRCs. A detailed description of the procedures required for cell collection and processing for immunohistochemical and immunofluorescent staining are provided. Collectively the 3D culture format described, combined with the primary CRC lines, provides an important medium- to high- throughput model system for biospecimen-based prostate research.
条件重编程细胞(CRCs)为原代细胞培养提供了一种可持续的方法,并具备建立大量患者来源细胞系“活生物样本库”的能力。对于多种类型的上皮细胞,已有多种三维(3D)培养方法被描述,这些方法能支持细胞达到更好的分化状态。虽然CRCs保留了它们对所分离组织的谱系定向,但在正常二维(2D)培养条件下生长时,它们无法表达许多与起源组织相关的分化标志物。为了增强患者来源的CRCs在前列腺癌研究中的应用,已定义了一种3D培养形式,该形式能使正常和肿瘤来源的前列腺上皮细胞快速(总共2周)向管腔细胞分化。本文描述了一种基于滤膜插入物的形式,用于正常和恶性前列腺CRCs的培养和分化。还提供了细胞收集以及用于免疫组织化学和免疫荧光染色的处理所需程序的详细说明。总体而言,所描述的3D培养形式与原代CRCs细胞系相结合,为基于生物样本的前列腺研究提供了一个重要的中高通量模型系统。