Montanez-Sauri Sara I, Beebe David J, Sung Kyung Eun
Materials Science Program, University of Wisconsin-Madison, Madison, WI, USA.
Cell Mol Life Sci. 2015 Jan;72(2):237-49. doi: 10.1007/s00018-014-1738-5. Epub 2014 Oct 2.
The increasing interest in studying cells using more in vivo-like three-dimensional (3D) microenvironments has created a need for advanced 3D screening platforms with enhanced functionalities and increased throughput. 3D screening platforms that better mimic in vivo microenvironments with enhanced throughput would provide more in-depth understanding of the complexity and heterogeneity of microenvironments. The platforms would also better predict the toxicity and efficacy of potential drugs in physiologically relevant conditions. Traditional 3D culture models (e.g., spinner flasks, gyratory rotation devices, non-adhesive surfaces, polymers) were developed to create 3D multicellular structures. However, these traditional systems require large volumes of reagents and cells, and are not compatible with high-throughput screening (HTS) systems. Microscale technology offers the miniaturization of 3D cultures and allows efficient screening of various conditions. This review will discuss the development, most influential works, and current advantages and challenges of microscale culture systems for screening cells in 3D microenvironments.
利用更类似体内的三维(3D)微环境来研究细胞的兴趣日益增加,这就需要具有增强功能和更高通量的先进3D筛选平台。能够更好地模拟体内微环境并提高通量的3D筛选平台,将能更深入地了解微环境的复杂性和异质性。这些平台还能在生理相关条件下更好地预测潜在药物的毒性和疗效。传统的3D培养模型(如转瓶、旋转振荡装置、非粘附表面、聚合物)是为了创建3D多细胞结构而开发的。然而,这些传统系统需要大量的试剂和细胞,并且与高通量筛选(HTS)系统不兼容。微尺度技术实现了3D培养的小型化,并允许对各种条件进行高效筛选。本综述将讨论用于在3D微环境中筛选细胞的微尺度培养系统的发展、最具影响力的研究成果以及当前的优势和挑战。