PUBLICATION

A chemical screening procedure for glucocorticoid signaling with a zebrafish larva luciferase reporter system

Authors
Weger, B.D., Weger, M., Jung, N., Lederer, C., Bräse, S., and Dickmeis, T.
ID
ZDB-PUB-131021-6
Date
2013
Source
Journal of visualized experiments : JoVE   (79): (Journal)
Registered Authors
Dickmeis, Thomas, Lederer, Christin, Weger, Benjamin, Weger, Meltem
Keywords
none
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Female
  • Glucocorticoids/analysis
  • Glucocorticoids/metabolism*
  • Larva/metabolism
  • Luciferases/chemistry*
  • Luciferases/genetics
  • Luciferases/metabolism
  • Luminescent Measurements/methods*
  • Male
  • Signal Transduction
  • Zebrafish/genetics
  • Zebrafish/metabolism*
PubMed
24056611 Full text @ J. Vis. Exp.
Abstract

Glucocorticoid stress hormones and their artificial derivatives are widely used drugs to treat inflammation, but long-term treatment with glucocorticoids can lead to severe side effects. Test systems are needed to search for novel compounds influencing glucocorticoid signaling in vivo or to determine unwanted effects of compounds on the glucocorticoid signaling pathway. We have established a transgenic zebrafish assay which allows the measurement of glucocorticoid signaling activity in vivo and in real-time, the GRIZLY assay (Glucocorticoid Responsive In vivo Zebrafish Luciferase activitY). The luciferase-based assay detects effects on glucocorticoid signaling with high sensitivity and specificity, including effects by compounds that require metabolization or affect endogenous glucocorticoid production. We present here a detailed protocol for conducting chemical screens with this assay. We describe data acquisition, normalization, and analysis, placing a focus on quality control and data visualization. The assay provides a simple, time-resolved, and quantitative readout. It can be operated as a stand-alone platform, but is also easily integrated into high-throughput screening workflows. It furthermore allows for many applications beyond chemical screening, such as environmental monitoring of endocrine disruptors or stress research.

Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping