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Real‐time 2 D visualization of metabolic activities in zebrafish embryos using a microfluidic technology
Author(s) -
Zhu Feng,
Baker Daniel,
Skommer Joanna,
Sewell Mary,
Wlodkowic Donald
Publication year - 2015
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.22662
Subject(s) - microfluidics , zebrafish , nanotechnology , visualization , computer science , biology , biochemical engineering , microbiology and biotechnology , materials science , engineering , data mining , biochemistry , gene
Non‐invasive and real‐time visualization of metabolic activities in living small model organisms such as embryos and larvae of zebrafish has not yet been attempted largely due to profound analytical limitations of existing technologies. Historically, our capacity to examine oxygen gradients surrounding eggs and embryos has been severely limited, so much so that to date, most of the articles characterizing in situ oxygen gradients have described predominantly mathematical simulations. These drawbacks can, however, be experimentally addressed by an emerging field of microfluidic Lab‐on‐a‐Chip (LOC) technologies combined with sophisticated optoelectronic sensors. In this work, we outline a proof‐of‐concept approach utilizing microfluidic living embryo array system to enable in situ Fluorescence Ratiometric Imaging (FRIM) on developing zebrafish embryos. The FRIM is an innovative method for kinetic quantification of the temporal patterns of aqueous oxygen gradients at a very fine scale based on signals coming from an optical sensor referred to as a sensor foil. We envisage that future integration of microfluidic chip‐based technologies with FRIM represents a noteworthy direction to miniaturize and revolutionize research on metabolism and physiology in vivo. © 2015 International Society for Advancement of Cytometry