The VerIFAST: an integrated method for cell isolation and extracellular/intracellular staining

被引:52
作者
Casavant, Benjamin P. [1 ]
Guckenberger, David J. [1 ]
Berry, Scott M. [1 ]
Tokar, Jacob T. [1 ]
Lang, Joshua M. [2 ]
Beebe, David J. [1 ]
机构
[1] Univ Wisconsin Madison, Wisconsin Inst Med Res, Dept Biomed Engn, Madison, WI 53715 USA
[2] Univ Wisconsin Madison, Wisconsin Inst Med Res, Dept Med, Madison, WI USA
基金
比尔及梅琳达.盖茨基金会;
关键词
CIRCULATING TUMOR-CELLS; CYTOMETRY; CAPTURE; BLOOD;
D O I
10.1039/c2lc41136a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Isolation and characterization of a specific subset of cells from a large heterogeneous population is necessary for studying rare subpopulations of cells. Existing methods require transfer or wash steps that risk causing loss of the rare cell population of interest. Integrated methods reduce loss, making these methods especially useful for reliable isolation of rare cell populations. In this report, we demonstrate the VerIFAST, a device that builds upon the simplified workflow of the Immiscible Filtration Assisted by Surface Tension (IFAST) to integrate a method for cellular isolation with methods for extra- and intracellular staining. First, a front-end purification step allows cells and unwanted particulates to passively settle out of the operational path of the paramagnetic particles, resulting in good efficiency of capture (>80%) and purity (>70%) with a single virtual wall traverse. Second, a Sieve Chamber is used downstream of the isolation chamber that removes excess unbound paramagnetic particles (PMPs) and performs complex multi-step washing procedures without centrifugation or transfer steps. Further, cellular staining can be performed in the device and is demonstrated for extracellular epithelial cell adhesion molecule (EpCAM), intracellular pan-cytokeratins, and Ki-67.
引用
收藏
页码:391 / 396
页数:6
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