ElectroTaxis-on-a-Chip (ETC): an integrated quantitative high-throughput screening platform for electrical field-directed cell migration

被引:15
|
作者
Zhao, Siwei [1 ]
Zhu, Kan [2 ,3 ]
Zhang, Yan [3 ]
Zhu, Zijie [1 ]
Xu, Zhengping [3 ]
Zhao, Min [2 ]
Pan, Tingrui [1 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Micronano Innovat MiNI Lab, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Dermatol, Davis, CA 95616 USA
[3] Zhejiang Univ, Sch Med, Dept Environm Med, Hangzhou, Zhejiang, Peoples R China
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SPINAL-CORD HEMISECTION; STIMULATION; REGENERATION; RECOVERY; FUTURE;
D O I
10.1039/c4lc00745j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Both endogenous and externally applied electrical stimulation can affect a wide range of cellular functions, including growth, migration, differentiation and division. Among those effects, the electrical field (EF)-directed cell migration, also known as electrotaxis, has received broad attention because it holds great potential in facilitating clinical wound healing. Electrotaxis experiment is conventionally conducted in centimetre-sized flow chambers built in Petri dishes. Despite the recent efforts to adapt microfluidics for electrotaxis studies, the current electrotaxis experimental setup is still cumbersome due to the needs of an external power supply and EF controlling/monitoring systems. There is also a lack of parallel experimental systems for high-throughput electrotaxis studies. In this paper, we present a first independently operable microfluidic platform for high-throughput electrotaxis studies, integrating all functional components for cell migration under EF stimulation (except microscopy) on a compact footprint (the same as a credit card), referred to as ElectroTaxis-on-a-Chip (ETC). Inspired by the R-2R resistor ladder topology in digital signal processing, we develop a systematic approach to design an infinitely expandable microfluidic generator of EF gradients for high-throughput and quantitative studies of EF-directed cell migration. Furthermore, a vacuum-assisted assembly method is utilized to allow direct and reversible attachment of our device to existing cell culture media on biological surfaces, which separates the cell culture and device preparation/fabrication steps. We have demonstrated that our ETC platform is capable of screening human cornea epithelial cell migration under the stimulation of an EF gradient spanning over three orders of magnitude. The screening results lead to the identification of the EF-sensitive range of that cell type, which can provide valuable guidance to the clinical application of EF-facilitated wound healing.
引用
收藏
页码:4398 / 4405
页数:8
相关论文
共 50 条
  • [31] Impedimetric immunosensor with on-chip integrated electrodes for high-throughput screening of liver fibrosis markers
    Huang, H. -H.
    Zhou, J.
    Huang, Y. -P.
    Kong, J. -L.
    JOURNAL OF ANALYTICAL CHEMISTRY, 2008, 63 (05) : 492 - 498
  • [32] A combined high-throughput and high-content platform for unified on-chip synthesis, characterization and biological screening
    Maximilian Benz
    Arndt Asperger
    Meike Hamester
    Alexander Welle
    Stefan Heissler
    Pavel A. Levkin
    Nature Communications, 11
  • [33] An Integrated Microfluidic Cell Array for High-throughput and High-content Drug Screening
    Song, H. X.
    Chen, Tan
    Zhang, B. Y.
    Ma, Y. F.
    Wang, Z. H.
    2009 2ND INTERNATIONAL SYMPOSIUM ON APPLIED SCIENCES IN BIOMEDICAL AND COMMUNICATION TECHNOLOGIES (ISABEL 2009), 2009, : 171 - 174
  • [34] A combined high-throughput and high-content platform for unified on-chip synthesis, characterization and biological screening
    Benz, Maximilian
    Asperger, Arndt
    Hamester, Meike
    Welle, Alexander
    Heissler, Stefan
    Levkin, Pavel A.
    NATURE COMMUNICATIONS, 2020, 11 (01)
  • [35] High-Throughput Toxicity and Phenotypic Screening of 3D Human Neural Progenitor Cell Cultures on a Microarray Chip Platform
    Nierode, Gregory J.
    Perea, Brian C.
    McFarland, Sean K.
    Pascoal, Jorge F.
    Clark, Douglas S.
    Schaffer, David V.
    Dordick, Jonathan S.
    STEM CELL REPORTS, 2016, 7 (05): : 970 - 982
  • [36] Biomolecular screening of formylpeptide receptor ligands with a sensitive, quantitative, high-throughput flow cytometry platform
    Edwards, Bruce S.
    Young, Susan M.
    Oprea, Tudor I.
    Bologa, Cristian G.
    Prossnitz, Eric R.
    Sklar, Larry A.
    NATURE PROTOCOLS, 2006, 1 (01) : 59 - 66
  • [37] Biomolecular screening of formylpeptide receptor ligands with a sensitive, quantitative, high-throughput flow cytometry platform
    Bruce S Edwards
    Susan M Young
    Tudor I Oprea
    Cristian G Bologa
    Eric R Prossnitz
    Larry A Sklar
    Nature Protocols, 2006, 1 : 59 - 66
  • [38] A modular versatile chip carrier for high-throughput screening of cell-biomaterial interactions
    Unadkat, H. V.
    Rewagad, R. R.
    Hulsman, M.
    Hulshof, G. F. B.
    Truckenmuller, R. K.
    Stamatialis, D. F.
    Reinders, M. J. T.
    Eijkel, J. C. T.
    van den Berg, A.
    van Blitterswijk, C. A.
    de Boer, J.
    JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2013, 10 (78)
  • [39] High-throughput cell-based screening system with on-chip dilution stage
    Greve, F.
    Seemann, L.
    Bonneick, S.
    Lichtenberg, J.
    Hierlemann, A.
    2006 INTERNATIONAL CONFERENCE ON MICROTECHNOLOGIES IN MEDICINE AND BIOLOGY, 2006, : 191 - +
  • [40] Identifying environmental chemicals as agonists of the androgen receptor by using a quantitative high-throughput screening platform
    Lynch, Caitlin
    Sakamuru, Srilatha
    Huang, Ruili
    Stavreva, Diana A.
    Varticovski, Lyuba
    Hager, Gordon L.
    Judson, Richard S.
    Houck, Keith A.
    Kleinstreuer, Nicole C.
    Casey, Warren
    Paules, Richard S.
    Simeonov, Anton
    Xia, Menghang
    TOXICOLOGY, 2017, 385 : 48 - 58