Programmable Interactions of Functionalized Single Bioparticles in a Dielectrophoresis-Based Microarray Chip

被引:35
作者
Abonnenc, Melanie [1 ]
Manaresi, Nicolo [1 ]
Borgatti, Monica [2 ,3 ]
Medoro, Gianni [1 ]
Fabbri, Enrica [2 ]
Romani, Aldo [4 ]
Altomare, Luigi [4 ]
Tartagni, Marco [4 ]
Rizzo, Roberta [5 ]
Baricordi, Olavio [5 ]
Tremante, Elisa [6 ]
Lo Monaco, Elisa [6 ]
Giacomini, Patrizio [6 ]
Guerrieri, Roberto [4 ]
Gambari, Roberto [2 ,3 ]
机构
[1] Silicon Biosyst, Bologna, Italy
[2] Univ Ferrara, Lab Dev Pharmacol & Pharmacogen Therapy Thalassem, Ctr Biotechnol, I-44100 Ferrara, Italy
[3] Univ Ferrara, ER GenTech, Dept Life Sci & Biotechnol, Mol Biol Sect, I-44100 Ferrara, Italy
[4] Univ Bologna, Ctr Excellence Elect Syst ARCES, I-40126 Bologna, Italy
[5] Univ Ferrara, Dept Expt & Diagnost Med, Sect Human Genet, I-44100 Ferrara, Italy
[6] Regina Elena Inst Canc Res, Immunol Lab, Rome, Italy
关键词
TUMOR-CELLS; HLA-G; SEPARATION; MANIPULATION; EXPRESSION; ANTIGEN; MICROFLUIDICS; MICROSPHERES; LABORATORIES; TWEEZERS;
D O I
10.1021/ac401296m
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Manipulating single biological objects is a major unmet challenge of biomedicine. Herein, we describe a lab-on-a-chip platform based on dielectrophoresis (DEP). The DEParray is a prototypal version consisting of 320 x 320 arrayed electrodes generating >10 000 spherical DEP cages. It allows the capture. and software-guided movement to predetermined spatial coordinates of single biological objects. With the DEParray we demonstrate (a) forced interaction between a single, preselected target cell and a programmable number of either microspheres or natural killer (NK) cells, (b) on-chip immunophenotypic discrimination of individual cells based on differential rosetting with microspheres functionalized with monoclonal antibodies to an inhibitory NK cell ligand (HLA-G), (c) on-chip, real-time (few minutes) assessment of immune lysis by either visual inspection or semiautomated, time-lapse reading of a fluorescent dye released from NK cell-sensitive targets, and (d) manipulation and immunophenotyping with limiting amounts (about 500) cells. To our knowledge, this is the first report describing a DEP-based lab-on-a-chip platform for the quick, arrayed, software-guided binding of individually moved biological objects, the targeting of single cells with microspheres, and the real-time characterization of immunophenotypes. The DEParray candidates as a discovery tool for novel cell:cell interactions with no prior (immuno)phenotypic knowledge.
引用
收藏
页码:8219 / 8224
页数:6
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