A microfluidic toolbox for cell fusion

被引:13
作者
Chiu, Flora W. Y. [1 ]
Bagci, Hakan [2 ]
Fisher, Amanda G. [2 ]
deMello, Andrew J. [1 ]
Elvira, Katherine S. [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[2] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp Campus, Lymphocyte Dev Grp, MRC Clin Sci Ctr, London W12 0NN, England
基金
欧洲研究理事会;
关键词
droplet microfluidics; cell fusion; cell encapsulation; single-cell; high efficiency; cell sorting; HIGH-THROUGHPUT; SINGLE-CELLS; ENCAPSULATION; MECHANISMS; ELECTROFUSION; PLURIPOTENCY; ANTIBODY; STATE; DROP; FLOW;
D O I
10.1002/jctb.4803
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cellular fusion is a key process in many fields ranging from historical gene mapping studies and monoclonal antibody production, through to cell reprogramming. Traditional methodologies for cell fusion rely on the random pairing of different cell types and generally result in low and variable fusion efficiencies. These approaches become particularly limiting where substantial numbers of bespoke one-to-one fusions are required, for example, for in-depth studies of nuclear reprogramming mechanisms. In recent years, microfluidic technologies have proven valuable in creating platforms where the manipulation of single cells is highly efficient, rapid and controllable. These technologies also allow the integration of different experimental steps and characterisation processes into a single platform. Although the application of microfluidic methodologies to cell fusion studies is promising, current technologies that rely on static trapping are limited both in terms of the overall number of fused cells produced and their experimental accessibility. Here we review some of the most exciting breakthroughs in core microfluidic technologies that will allow the creation of integrated platforms for controlled cell fusion at high throughput. (c) 2015 Society of Chemical Industry
引用
收藏
页码:16 / 24
页数:9
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