Miniaturized Embryo Array for Automated Trapping, Immobilization and Microperfusion of Zebrafish Embryos
- Authors
- Akagi, J., Khoshmanesh, K., Evans, B., Hall, C.J., Crosier, K.E., Cooper, J.M., Crosier, P.S., and Wlodkowic, D.
- ID
- ZDB-PUB-120522-16
- Date
- 2012
- Source
- PLoS One 7(5): e36630 (Journal)
- Registered Authors
- Crosier, Kathy, Crosier, Phil, Hall, Chris
- Keywords
- none
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Computer Systems
- Drug Delivery Systems
- Embryo Culture Techniques
- Equipment Design
- Hydrodynamics
- Microfluidic Analytical Techniques/instrumentation*
- Microfluidic Analytical Techniques/methods
- Miniaturization
- Models, Animal
- Neovascularization, Physiologic
- Perfusion
- Time-Lapse Imaging
- Zebrafish/embryology*
- Zebrafish/genetics
- PubMed
- 22606275 Full text @ PLoS One
Zebrafish (Danio rerio) has recently emerged as a powerful experimental model in drug discovery and environmental toxicology. Drug discovery screens performed on zebrafish embryos mirror with a high level of accuracy the tests usually performed on mammalian animal models, and fish embryo toxicity assay (FET) is one of the most promising alternative approaches to acute ecotoxicity testing with adult fish. Notwithstanding this, automated in-situ analysis of zebrafish embryos is still deeply in its infancy. This is mostly due to the inherent limitations of conventional techniques and the fact that metazoan organisms are not easily susceptible to laboratory automation. In this work, we describe the development of an innovative miniaturized chip-based device for the in-situ analysis of zebrafish embryos. We present evidence that automatic, hydrodynamic positioning, trapping and long-term immobilization of single embryos inside the microfluidic chips can be combined with time-lapse imaging to provide real-time developmental analysis. Our platform, fabricated using biocompatible polymer molding technology, enables rapid trapping of embryos in low shear stress zones, uniform drug microperfusion and high-resolution imaging without the need of manual embryo handling at various developmental stages. The device provides a highly controllable fluidic microenvironment and post-analysis eleuthero-embryo stage recovery. Throughout the incubation, the position of individual embryos is registered. Importantly, we also for first time show that microfluidic embryo array technology can be effectively used for the analysis of anti-angiogenic compounds using transgenic zebrafish line (fli1a:EGFP). The work provides a new rationale for rapid and automated manipulation and analysis of developing zebrafish embryos at a large scale.