Microfluidic device for mechanical dissociation of cancer cell aggregates into single cells

• Published in: Lab on a chip Vol. 15; no. 1; pp. 339 - 350
• Main Authors: Qiu, Xiaolong, De Jesus, Janice, Pennell, Marissa, Troiani, Marco, Haun, Jered B
• Format: Journal Article
• Language: English
• Published: England 07.01.2015
• Subjects: Cancer; Cell Line, Tumor; Cell Survival - physiology; Channels; Computational fluid dynamics; Devices; Digestion; Equipment Design; Flow Cytometry - instrumentation; Flow Cytometry - methods; Fluid flow; Humans; Microfluidic Analytical Techniques - instrumentation; Microfluidic Analytical Techniques - methods; Microfluidics; Models, Biological; Neoplasms; Spheroids, Cellular - cytology; Tumor Cells, Cultured; Tumors
• ISSN: 1473-0197; 1473-0189
• DOI: 10.1039/c4lc01126k

Tumors tissues house a diverse array of cell types, requiring powerful cell-based analysis methods to characterize cellular heterogeneity and identify rare cells. Tumor tissue is dissociated into single cells by treatment with proteolytic enzymes, followed by mechanical disruption using vortexing or pipetting. These procedures can be incomplete and require significant time, and the latter mechanical treatments are poorly defined and controlled. Here, we present a novel microfluidic device to improve mechanical dissociation of digested tissue and cell aggregates into single cells. The device design includes a network of branching channels that range in size from millimeters down to hundreds of microns. The channels also contain flow constrictions that generate well-defined regions of high shear force, which we refer to as "hydrodynamic micro-scalpels", to progressively disaggregate tissue fragments and clusters into single cells. We show using in vitro cancer cell models that the microfluidic device significantly enhances cell recovery in comparison to mechanical disruption by pipetting and vortexing after digestion with trypsin or incubation with EDTA. Notably, the device enabled superior results to be obtained after shorter proteolytic digestion times, resulting in fully viable cells in less than ten minutes. The device could also be operated under enzyme-free conditions that could better maintain expression of certain surface markers. The microfluidic format is advantageous because it enables application of well-defined mechanical forces and rapid processing times. Furthermore, it may be possible to directly integrate downstream processing and detection operations to create integrated cell-based analysis platforms. The enhanced capabilities enabled by our novel device may help promote applications of single cell detection and purification techniques to tumor tissue specimens, advancing the current understanding of cancer biology and enabling molecular diagnostics in clinical settings.