Center for Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Anal Chem. 2011 Jun 1;83(11):4118-25. doi: 10.1021/ac200267t. Epub 2011 May 3.
Traditional high-throughput screening (HTS) is carried out in centralized facilities that require extensive robotic liquid and plate handling equipment. This model of HTS is restrictive as such facilities are not accessible to many researchers. We have designed a simple microarray platform for cell-based screening that can be carried out at the benchtop. The device creates a microarray of 2100 individual cell-based assays in a standard microscope slide format. A microarray of chemical-laden hydrogels addresses a matching array of cell-laden microwells thus creating a microarray of sealed microscale cell cultures each with unique conditions. We demonstrate the utility of the device by screening the extent of apoptosis and necrosis in MCF-7 breast cancer cells in response to exposure to a small library of chemical compounds. From a set of screens we produced a rank order of chemicals that preferentially induce apoptosis over necrosis in MCF-7 cells. Treatment with doxorubicin induced high levels of apoptosis in comparison with staurosporine, ethanol, and hydrogen peroxide, whereas treatment with 100 μM ethanol induced minimal apoptosis with high levels of necrosis. We anticipate broad application of the device for various research and discovery applications as it is easy to use, scalable, and can be fabricated and operated with minimal peripheral equipment.
传统的高通量筛选(HTS)是在需要广泛的机器人液体和板处理设备的集中设施中进行的。这种 HTS 模型具有限制性,因为许多研究人员无法使用这些设施。我们设计了一种简单的基于细胞的筛选微阵列平台,可以在台式机上进行。该设备以标准显微镜载玻片格式创建了 2100 个单独的基于细胞的测定的微阵列。载有化学物质的微阵列与载有细胞的微孔的匹配阵列相吻合,从而创建了具有独特条件的密封微尺度细胞培养物的微阵列。我们通过筛选 MCF-7 乳腺癌细胞暴露于一小部分化学化合物后凋亡和坏死的程度来证明该设备的实用性。从一组筛选中,我们产生了一种化学物质的等级顺序,这些化学物质优先诱导 MCF-7 细胞中的凋亡而不是坏死。与 staurosporine、乙醇和过氧化氢相比,阿霉素处理诱导高水平的凋亡,而 100 μM 乙醇处理诱导高水平的坏死,凋亡水平最低。我们预计该设备将广泛应用于各种研究和发现应用,因为它易于使用、可扩展,并且可以使用最少的外围设备进行制造和操作。