Fakhouri Abdulaziz S, Leight Jennifer L
Department of Biomedical Engineering, The Ohio State University; The Ohio State University Comprehensive Cancer Center, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute; Biomedical Technology Department, King Saud University.
Department of Biomedical Engineering, The Ohio State University; The Ohio State University Comprehensive Cancer Center, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute;
J Vis Exp. 2019 Jan 22(143). doi: 10.3791/59123.
Three-dimensional (3D) cell culture systems often more closely recapitulate in vivo cellular responses and functions than traditional two-dimensional (2D) culture systems. However, measurement of cell function in 3D culture is often more challenging. Many biological assays require retrieval of cellular material which can be difficult in 3D cultures. One way to address this challenge is to develop new materials that enable measurement of cell function within the material. Here, a method is presented for measurement of cellular matrix metalloproteinase (MMP) activity in 3D hydrogels in a 96-well format. In this system, a poly(ethylene glycol) (PEG) hydrogel is functionalized with a fluorogenic MMP cleavable sensor. Cellular MMP activity is proportional to fluorescence intensity and can be measured with a standard microplate reader. Miniaturization of this assay to a 96-well format reduced the time required for experimental set up by 50% and reagent usage by 80% per condition as compared to the previous 24-well version of the assay. This assay is also compatible with other measurements of cellular function. For example, a metabolic activity assay is demonstrated here, which can be conducted simultaneously with MMP activity measurements within the same hydrogel. The assay is demonstrated with human melanoma cells encapsulated across a range of cell seeding densities to determine the appropriate encapsulation density for the working range of the assay. After 24 h of cell encapsulation, MMP and metabolic activity readouts were proportional to cell seeding density. While the assay is demonstrated here with one fluorogenic degradable substrate, the assay and methodology could be adapted for a wide variety of hydrogel systems and other fluorescent sensors. Such an assay provides a practical, efficient and easily accessible 3D culturing platform for a wide variety of applications.
与传统的二维(2D)培养系统相比,三维(3D)细胞培养系统通常能更紧密地模拟体内细胞反应和功能。然而,在3D培养中测量细胞功能往往更具挑战性。许多生物学检测需要获取细胞材料,而这在3D培养中可能很困难。解决这一挑战的一种方法是开发能够在材料内测量细胞功能的新材料。在此,介绍一种以96孔板形式测量3D水凝胶中细胞基质金属蛋白酶(MMP)活性的方法。在该系统中,聚乙二醇(PEG)水凝胶用一种可被MMP切割的荧光传感器进行功能化修饰。细胞MMP活性与荧光强度成正比,可使用标准微孔板读数仪进行测量。与之前的24孔板检测版本相比,将该检测小型化为96孔板形式,每个条件下实验设置所需时间减少了50%,试剂用量减少了80%。该检测还与细胞功能的其他测量方法兼容。例如,这里展示了一种代谢活性检测方法,它可以与同一水凝胶内的MMP活性测量同时进行。用人黑色素瘤细胞以一系列细胞接种密度进行包封,以确定该检测工作范围内合适的包封密度,从而证明了该检测方法。细胞包封24小时后,MMP和代谢活性读数与细胞接种密度成正比。虽然这里用一种荧光可降解底物证明了该检测方法,但该检测方法和方法学可适用于多种水凝胶系统和其他荧光传感器。这样的检测为各种应用提供了一个实用、高效且易于使用的3D培养平台。