Separation of neural stem cells by whole cell membrane capacitance using dielectrophoresis

被引:51
作者
Adams, Tayloria N. G. [1 ,2 ,3 ]
Jiang, Alan Y. L. [1 ,2 ,3 ]
Vyas, Prema D. [2 ,3 ]
Flanagan, Lisa A. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Neurol, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Sue & Bill Gross Stem Cell Res Ctr, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Anat & Neurobiol, Irvine, CA 92697 USA
基金
美国国家科学基金会;
关键词
Neural stem cell; Progenitor cell; Dielectrophoresis; Membrane capacitance; Cell sorting; Microfluidics; DIFFERENTIATION; ENRICHMENT; CANCER;
D O I
10.1016/j.ymeth.2017.08.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Whole cell membrane capacitance is an electrophysiological property of the plasma membrane that serves as a biomarker for stem cell fate potential. Neural stem and progenitor cells (NSPCs) that differ in ability to form neurons or astrocytes are distinguished by membrane capacitance measured by dielectrophoresis (DEP). Differences in membrane capacitance are sufficient to enable the enrichment of neuron- or astrocyte-forming cells by DEP, showing the separation of stem cells on the basis of fate potential by membrane capacitance. NSPCs sorted by DEP need not be labeled and do not experience toxic effects from the sorting procedure. Other stem cell populations also display shifts in membrane capacitance as cells differentiate to a particular fate, clarifying the value of sorting a variety of stem cell types by capacitance. Here, we describe methods developed by our lab for separating NSPCs on the basis of capacitance using several types of DEP microfluidic devices, providing basic information on the sorting procedure as well as specific advantages and disadvantages of each device. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:91 / 103
页数:13
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