Department of Chemical Engineering, Texas Tech University, Lubbock, TX 79409, United States.
Sci Rep. 2017 Feb 2;7:41707. doi: 10.1038/srep41707.
Drug assays with patient-derived cells such as circulating tumor cells requires manipulating small sample volumes without loss of rare disease-causing cells. Here, we report an effective technology for isolating and analyzing individual tumor cells and their clusters from minute sample volumes using an optimized microfluidic device integrated with pipettes. The method involves using hand pipetting to create an array of cell-laden nanoliter-sized droplets immobilized in a microfluidic device without loss of tumor cells during the pipetting process. Using this technology, we demonstrate single-cell analysis of tumor cell response to the chemotherapy drug doxorubicin. We find that even though individual tumor cells display diverse uptake profiles of the drug, the onset of apoptosis is determined by accumulation of a critical intracellular concentration of doxorubicin. Experiments with clusters of tumor cells compartmentalized in microfluidic drops reveal that cells within a cluster have higher viability than their single-cell counterparts when exposed to doxorubicin. This result suggests that circulating tumor cell clusters might be able to better survive chemotherapy drug treatment. Our technology is a promising tool for understanding tumor cell-drug interactions in patient-derived samples including rare cells.
利用患者来源的细胞(如循环肿瘤细胞)进行药物检测需要在不损失稀有致病细胞的情况下处理小样本量。在这里,我们报告了一种有效的技术,该技术使用经过优化的微流控设备与移液管集成,可从微小的样本量中分离和分析单个肿瘤细胞及其簇。该方法涉及使用手动移液来创建一系列含有细胞的纳升级大小的液滴阵列,在移液过程中不会损失肿瘤细胞。使用这项技术,我们展示了对肿瘤细胞对化疗药物阿霉素反应的单细胞分析。我们发现,尽管单个肿瘤细胞对药物的摄取模式存在差异,但细胞凋亡的发生是由阿霉素在细胞内达到临界浓度决定的。在微流控液滴中分隔的肿瘤细胞簇的实验表明,与单个细胞相比,当暴露于阿霉素时,簇内的细胞具有更高的活力。这一结果表明,循环肿瘤细胞簇可能能够更好地耐受化疗药物治疗。我们的技术是一种有前途的工具,可用于研究包括稀有细胞在内的患者来源样本中的肿瘤细胞-药物相互作用。