Dechorionation

Dechorionation is the removal of the chorion, the protective acellular envelope surrounding an embryo, and is a common technique in developmental biology. In zebrafish research, embryos are typically treated with a proteolytic enzyme such as pronase, which digests chorion proteins and loosens the envelope for gentle removal with forceps or mechanical agitation. This process improves access to the developing embryo for microinjection, imaging, drug exposure, and cell or tissue manipulation. By reducing a physical barrier while preserving embryonic viability, dechorionation supports precise studies of early development, toxicology, disease mechanisms, and experimental treatments.

Dechorionation - Related Videos

Research

JoVE EoE - Drosophila melanogaster (fruit fly)

Drosophila Egg Collection and Dechorionation: A Method to Remove the Outermost Egg Layer

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2023

The Drosophila embryo is surrounded by protective outer membranes. To gain access to the embryo, the chorion–the outermost of the membranes–is often removed. This video describes a commonly used method of dechorionation using sodium hypochlorite. The example protocol demonstrates the procedure while employing sterile techniques necessary for axenic or gnotobiotic animal rearing.

Research

JoVE Journal - Biology
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Dechorionation of Medaka Embryos and Cell Transplantation for the Generation of Chimeras

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Cited by 20 •

2010

Due to the hard chorion and soft embryos, manipulation of medaka embryos is more involved than in zebrafish. This video shows step-by-step procedures for how to manipulate medaka embryos, including dechorionation, mounting in agarose for imaging and cell transplantation for the production of chimeras. These procedures are essential to use medaka and zebrafish in a laboratory to take full advantage of their complementary features for the genetic dissection of vertebrate genome functions.

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis

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Cited by 17 •

2016

We present transient transgenesis and gene knockdown in Ciona intestinalis, a chordate sister group to vertebrates, using microinjection and electroporation techniques. Such methods facilitate functional genomics in this simple invertebrate that features rudimentary characteristics of vertebrates, including notochord and head sensory epithelia, and many orthologs of human disease associated genes.

In Vivo Imaging of Transgenic Gene Expression in Individual Retinal Progenitors in Chimeric Zebrafish Embryos to Study Cell Nonautonomous Influences

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Cited by 2 •

2017

Live tracking of individual WT retinal progenitors in distinct genetic backgrounds allows for the assessment of the contribution of cell non-autonomous signaling during neurogenesis. Here, a combination of gene knockdown, chimera generation via embryo transplantation and in vivo time-lapse confocal imaging was utilized for this purpose.

Layered Agar Mounting: Preparing Live Zebrafish Embryos for Long-Term Imaging with an Inverted Microscope

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2023

This article describes a method to mount live zebrafish embryos for long term imaging. This method is cost effective and easy to perform using regular glass-bottom microscopy dishes for imaging on Inverted Microscope. The mounting is performed in layers of agarose at different concentrations.

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