Stewart Teneale A, Davis Felicity M
Mater Research-The University of Queensland, Faculty of Medicine, Brisbane, Queensland 4102, Australia.
Translational Research Institute, Brisbane, Queensland 4102, Australia.
ACS Pharmacol Transl Sci. 2020 Jan 15;3(1):63-75. doi: 10.1021/acsptsci.9b00090. eCollection 2020 Feb 14.
An essential process in predicting the pharmacological activity of a candidate molecule involves the evaluation of target responses using established model systems. While these models largely comprise immortalized cells, which are often serially passaged as monolayers on uniformly stiff substrates and are modified to overexpress one or more components of the pathway-of-interest, the importance of cell identity, heterogeneity, and three-dimensional (3D) context to target response is gaining increasing attention. Here, we assess intracellular calcium responses in mouse mammary epithelial cells in three distinct model systems: 3D primary organoids, 2D primary epithelial cells, and 2D immortalized cells. Specifically, we assess intracellular calcium responses to a number of extracellular signals implicated in the regulation of basal (or myoepithelial) cell function. These findings provide further insights into cell type and context-specific pharmacological responses in mammary epithelial cells and highlight the opportunities and challenges in the adoption of architecturally complex and heterogeneous assays in pharmacological research.
预测候选分子药理活性的一个关键过程涉及使用既定的模型系统评估靶点反应。虽然这些模型主要由永生化细胞组成,这些细胞通常在均匀坚硬的底物上以单层形式连续传代,并经过修饰以过表达感兴趣通路的一个或多个组分,但细胞身份、异质性和三维(3D)环境对靶点反应的重要性正日益受到关注。在这里,我们在三种不同的模型系统中评估小鼠乳腺上皮细胞的细胞内钙反应:3D原代类器官、2D原代上皮细胞和2D永生化细胞。具体而言,我们评估细胞内钙对多种参与基础(或肌上皮)细胞功能调节的细胞外信号的反应。这些发现为乳腺上皮细胞中细胞类型和背景特异性药理反应提供了进一步的见解,并突出了在药理研究中采用结构复杂和异质性分析方法的机遇与挑战。