ZFIN ID: ZDB-PUB-121121-31
An assay for permeability of the zebrafish embryonic neuroepithelium
Chang, J.T., and Sive, H.
Date: 2012
Source: Journal of visualized experiments : JoVE   (68): e4242 (Journal)
Registered Authors: Chang, Jessica, Sive, Hazel
Keywords: none
MeSH Terms:
  • Animals
  • Cerebral Ventricles/embryology*
  • Cerebral Ventricles/metabolism*
  • Epithelium/embryology
  • Epithelium/metabolism
  • Fluorescent Dyes/chemistry
  • Fluorescent Dyes/pharmacokinetics
  • Microinjections
  • Zebrafish/embryology*
PubMed: 23128341 Full text @ J. Vis. Exp.
ABSTRACT

The brain ventricular system is conserved among vertebrates and is composed of a series of interconnected cavities called brain ventricles, which form during the earliest stages of brain development and are maintained throughout the animal's life. The brain ventricular system is found in vertebrates, and the ventricles develop after neural tube formation, when the central lumen fills with cerebrospinal fluid (CSF). CSF is a protein rich fluid that is essential for normal brain development and function.

In zebrafish, brain ventricle inflation begins at approximately 18 hr post fertilization (hpf), after the neural tube is closed. Multiple processes are associated with brain ventricle formation, including formation of a neuroepithelium, tight junction formation that regulates permeability and CSF production. We showed that the Na,K-ATPase is required for brain ventricle inflation, impacting all these processes, while claudin 5a is necessary for tight junction formation. Additionally, we showed that "relaxation" of the embryonic neuroepithelium, via inhibition of myosin, is associated with brain ventricle inflation.

To investigate the regulation of permeability during zebrafish brain ventricle inflation, we developed a ventricular dye retention assay. This method uses brain ventricle injection in a living zebrafish embryo, a technique previously developed in our lab, to fluorescently label the cerebrospinal fluid. Embryos are then imaged over time as the fluorescent dye moves through the brain ventricles and neuroepithelium. The distance the dye front moves away from the basal (non-luminal) side of the neuroepithelium over time is quantified and is a measure of neuroepithelial permeability (Figure 1). We observe that dyes 70 kDa and smaller will move through the neuroepithelium and can be detected outside the embryonic zebrafish brain at 24 hpf (Figure 2).

This dye retention assay can be used to analyze neuroepithelial permeability in a variety of different genetic backgrounds, at different times during development, and after environmental perturbations. It may also be useful in examining pathological accumulation of CSF. Overall, this technique allows investigators to analyze the role and regulation of permeability during development and disease.

ADDITIONAL INFORMATION No data available