PUBLICATION

A Multiparametric Assay Platform for Simultaneous In Vivo Assessment of Pronephric Morphology, Renal Function and Heart Rate in Larval Zebrafish

Authors
Steenbergen, P.J., Heigwer, J., Pandey, G., Tönshoff, B., Gehrig, J., Westhoff, J.H.
ID
ZDB-PUB-200524-16
Date
2020
Source
Cells   9(5): (Journal)
Registered Authors
Gehrig, Jochen
Keywords
automated imaging, developmental toxicity, heart rate, kidney function, kidney morphology, pronephros, screening, zebrafish
MeSH Terms
  • Animals
  • Biological Assay/methods*
  • Embryo, Nonmammalian/physiology
  • Fluorescein-5-isothiocyanate/metabolism
  • Heart Function Tests*
  • Heart Rate/physiology*
  • Kidney/physiology*
  • Larva/physiology
  • Pronephros/anatomy & histology*
  • Pronephros/embryology
  • Zebrafish/anatomy & histology*
  • Zebrafish/embryology
  • Zebrafish/physiology*
PubMed
32443839 Full text @ Cells
Abstract
Automated high-throughput workflows allow for chemical toxicity testing and drug discovery in zebrafish disease models. Due to its conserved structural and functional properties, the zebrafish pronephros offers a unique model to study renal development and disease at larger scale. Ideally, scoring of pronephric phenotypes includes morphological and functional assessments within the same larva. However, to efficiently upscale such assays, refinement of existing methods is required. Here, we describe the development of a multiparametric in vivo screening pipeline for parallel assessment of pronephric morphology, kidney function and heart rate within the same larva on a single imaging platform. To this end, we developed a novel 3D-printed orientation tool enabling multiple consistent orientations of larvae in agarose-filled microplates. Dorsal pronephros imaging was followed by assessing renal clearance and heart rates upon fluorescein isothiocyanate (FITC)-inulin microinjection using automated time-lapse imaging of laterally positioned larvae. The pipeline was benchmarked using a set of drugs known to induce developmental nephrotoxicity in humans and zebrafish. Drug-induced reductions in renal clearance and heart rate alterations were detected even in larvae exhibiting minor pronephric phenotypes. In conclusion, the developed workflow enables rapid and semi-automated in vivo assessment of multiple morphological and functional parameters.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping