Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Analyst. 2011 Feb 7;136(3):473-8. doi: 10.1039/c0an00609b. Epub 2010 Oct 21.
Culture of cells as three-dimensional (3D) aggregates can enhance in vitro tests for basic biological research as well as for therapeutics development. Such 3D culture models, however, are often more complicated, cumbersome, and expensive than two-dimensional (2D) cultures. This paper describes a 384-well format hanging drop culture plate that makes spheroid formation, culture, and subsequent drug testing on the obtained 3D cellular constructs as straightforward to perform and adapt to existing high-throughput screening (HTS) instruments as conventional 2D cultures. Using this platform, we show that drugs with different modes of action produce distinct responses in the physiological 3D cell spheroids compared to conventional 2D cell monolayers. Specifically, the anticancer drug 5-fluorouracil (5-FU) has higher anti-proliferative effects on 2D cultures whereas the hypoxia activated drug commonly referred to as tirapazamine (TPZ) are more effective against 3D cultures. The multiplexed 3D hanging drop culture and testing plate provides an efficient way to obtain biological insights that are often lost in 2D platforms.
细胞培养为三维(3D)聚集体可以增强基础生物学研究以及治疗药物开发的体外测试。然而,这种 3D 培养模型通常比二维(2D)培养更复杂、繁琐和昂贵。本文描述了一种 384 孔格式的悬滴培养板,它使得球体的形成、培养以及随后对获得的 3D 细胞构建体的药物测试变得简单,并且可以像传统的 2D 培养一样适应现有的高通量筛选(HTS)仪器。使用该平台,我们表明,具有不同作用模式的药物在生理 3D 细胞球体中产生与传统 2D 细胞单层明显不同的反应。具体而言,抗癌药物 5-氟尿嘧啶(5-FU)对 2D 培养物具有更高的抗增殖作用,而通常称为替拉扎明(TPZ)的缺氧激活药物对 3D 培养物更有效。该多路复用的 3D 悬滴培养和测试板提供了一种有效的方法,可以获得在 2D 平台中经常丢失的生物学见解。