Microfluidic Device for a Rapid Immobilization of Zebrafish Larvae in Environmental Scanning Electron Microscopy

被引:5
作者
Akagi, Jin [1 ]
Zhu, Feng [1 ]
Skommer, Joanna [1 ]
Hall, Chris J. [2 ]
Crosier, Philip S. [2 ]
Cialkowski, Michal [3 ]
Wlodkowic, Donald [1 ,3 ]
机构
[1] RMIT Univ, Sch Appl Sci, Melbourne, Vic 3083, Australia
[2] Univ Auckland, Dept Mol Med & Pathol, Auckland 1, New Zealand
[3] Poznan Univ Tech, Fac Machines & Transportat, Chair Thermal Engn, Poznan, Poland
基金
澳大利亚研究理事会;
关键词
Danio rerio; environmental scanning electron microscopy; imaging; immobilization; lab-on-a-chip; larvae; microfluidics; Zebrafish; ASSAYS; FISH;
D O I
10.1002/cyto.a.22603
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Small vertebrate model organisms have recently gained popularity as attractive experimental models that enhance our understanding of human tissue and organ development. Despite a large body of evidence using optical spectroscopy for the characterization of small model organism on chip-based devices, no attempts have been so far made to interface microfabricated technologies with environmental scanning electron microscopy (ESEM). Conventional scanning electron microscopy requires high vacuum environments and biological samples must be, therefore, submitted to many preparative procedures to dehydrate, fix, and subsequently stain the sample with gold-palladium deposition. This process is inherently low-throughput and can introduce many analytical artifacts. This work describes a proof-of-concept microfluidic chip-based system for immobilizing zebrafish larvae for ESEM imaging that is performed in a gaseous atmosphere, under low vacuum mode and without any need for sample staining protocols. The microfabricated technology provides a user-friendly and simple interface to perform ESEM imaging on zebrafish larvae. Presented lab-on-a-chip device was fabricated using a high-speed infrared laser micromachining in a biocompatible poly(methyl methacrylate) thermoplastic. It consisted of a reservoir with multiple semispherical microwells designed to hold the yolk of dechorionated zebrafish larvae. Immobilization of the larvae was achieved by a gentle suction generated during blotting of the medium. Trapping region allowed for multiple specimens to be conveniently positioned on the chip-based device within few minutes for ESEM imaging. (c) 2014 International Society for Advancement of Cytometry
引用
收藏
页码:190 / 194
页数:5
相关论文
共 14 条
[1]  
Akagi J, 2014, CURR PROTOC CYTOM, V67
[2]   Integrated chip-based physiometer for automated fish embryo toxicity biotests in pharmaceutical screening and ecotoxicology [J].
Akagi, Jin ;
Zhu, Feng ;
Hall, Chris J. ;
Crosier, Kathryn E. ;
Crosier, Philip S. ;
Wlodkowic, Donald .
CYTOMETRY PART A, 2014, 85A (06) :537-547
[3]   Fish on chips: Microfluidic living embryo array for accelerated in vivo angiogenesis assays [J].
Akagi, Jin ;
Khoshmanesh, Khashayar ;
Hall, Chris J. ;
Cooper, Jonathan M. ;
Crosier, Kathryn E. ;
Crosier, Philip S. ;
Wlodkowic, Donald .
SENSORS AND ACTUATORS B-CHEMICAL, 2013, 189 :11-20
[4]   Miniaturized Embryo Array for Automated Trapping, Immobilization and Microperfusion of Zebrafish Embryos [J].
Akagi, Jin ;
Khoshmanesh, Khashayar ;
Evans, Barbara ;
Hall, Chris J. ;
Crosier, Kathryn E. ;
Cooper, Jonathan M. ;
Crosier, Philip S. ;
Wlodkowic, Donald .
PLOS ONE, 2012, 7 (05)
[5]   An In Vivo Antilymphatic Screen in Zebrafish Identifies Novel Inhibitors of Mammalian Lymphangiogenesis and Lymphatic-Mediated Metastasis [J].
Astin, Jonathan W. ;
Jamieson, Stephen M. F. ;
Eng, Tiffany C. Y. ;
Flores, Maria V. ;
Misa, June P. ;
Chien, Annie ;
Crosier, Kathryn E. ;
Crosier, Philip S. .
MOLECULAR CANCER THERAPEUTICS, 2014, 13 (10) :2450-2462
[6]   DMXAA (Vadimezan, ASA404) is a multi-kinase inhibitor targeting VEGFR2 in particular [J].
Buchanan, Christina M. ;
Shin, Jen-Hsing ;
Astin, Jonathan W. ;
Rewcastle, Gordon W. ;
Flanagan, Jack U. ;
Crosier, Philip S. ;
Shepherd, Peter R. .
CLINICAL SCIENCE, 2012, 122 (9-10) :449-457
[7]   Infection-Responsive Expansion of the Hematopoietic Stem and Progenitor Cell Compartment in Zebrafish Is Dependent upon Inducible Nitric Oxide [J].
Hall, Christopher J. ;
Flores, Maria Vega ;
Oehlers, Stefan H. ;
Sanderson, Leslie E. ;
Lam, Enid Y. ;
Crosier, Kathryn E. ;
Crosier, Philip S. .
CELL STEM CELL, 2012, 10 (02) :198-209
[8]   Interfacing Cell-Based Assays in Environmental Scanning Electron Microscopy Using Dielectrophoresis [J].
Khoshmanesh, Khashayar ;
Akagi, Jin ;
Nahavandi, Saeid ;
Kalantar-zadeh, Kourosh ;
Baratchi, Sara ;
Williams, David E. ;
Cooper, Jonathan M. ;
Wlodkowic, Donald .
ANALYTICAL CHEMISTRY, 2011, 83 (08) :3217-3221
[9]   Animal models of human disease: zebrafish swim into view [J].
Lieschke, Graham J. ;
Currie, Peter D. .
NATURE REVIEWS GENETICS, 2007, 8 (05) :353-367
[10]   A critical overview of ESEM applications in the biological field [J].
Muscariello, L ;
Rosso, F ;
Marino, G ;
Giordano, A ;
Barbarisi, M ;
Cafiero, G ;
Barbarisi, A .
JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 205 (03) :328-334