PUBLICATION
Podocyte developmental defects caused by adriamycin in zebrafish embryos and larvae: a novel model of glomerular damage
- Authors
- Zennaro, C., Mariotti, M., Carraro, M., Pasqualetti, S., Corbelli, A., Armelloni, S., Li, M., Ikehata, M., Clai, M., Artero, M., Messa, P., Boscutti, G., Rastaldi, M.P.
- ID
- ZDB-PUB-140523-11
- Date
- 2014
- Source
- PLoS One 9: e98131 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Dose-Response Relationship, Drug
- Doxorubicin/pharmacology*
- Embryonic Development/drug effects*
- Heart/drug effects
- Heart/embryology
- Kidney Glomerulus/drug effects*
- Kidney Glomerulus/embryology*
- Kidney Glomerulus/metabolism
- Kidney Glomerulus/pathology
- Kidney Glomerulus/ultrastructure
- Larva
- Permeability/drug effects
- Podocytes/drug effects*
- Podocytes/metabolism
- Podocytes/ultrastructure
- Zebrafish/embryology*
- PubMed
- 24845233 Full text @ PLoS One
Citation
Zennaro, C., Mariotti, M., Carraro, M., Pasqualetti, S., Corbelli, A., Armelloni, S., Li, M., Ikehata, M., Clai, M., Artero, M., Messa, P., Boscutti, G., Rastaldi, M.P. (2014) Podocyte developmental defects caused by adriamycin in zebrafish embryos and larvae: a novel model of glomerular damage. PLoS One. 9:e98131.
Abstract
The zebrafish pronephros is gaining popularity in the nephrology community, because embryos are easy to cultivate in multiwell plates, allowing large number of experiments to be conducted in an in vivo model. In a few days, glomeruli reach complete development, with a structure that is similar to that of the mammalian counterpart, showing a fenestrated endothelium and a basement membrane covered by the multiple ramifications of mature podocytes. As a further advantage, zebrafish embryos are permeable to low molecular compounds, and this explains their extensive use in drug efficacy and toxicity experiments. Here we show that low concentrations of adriamycin (i.e. 10 and 20 μM), when dissolved in the medium of zebrafish embryos at 9 hours post-fertilization and removed after 48 hours (57 hpf), alter the development of podocytes with subsequent functional impairment, demonstrated by onset of pericardial edema and reduction of expression of the podocyte proteins nephrin and wt1. Podocyte damage is morphologically confirmed by electron microscopy and functionally supported by increased clearance of microinjected 70 kDa fluorescent dextran. Importantly, besides pericardial edema and glomerular damage, which persist and worsen after adriamycin removal from the medium, larvae exposed to adriamycin 10 and 20 μM do not show any myocardiocyte alterations nor vascular changes. The only extra-renal effect is a transient delay of cartilage formation that rapidly recovers once adriamycin is removed. In summary, this low dose adriamycin model can be applied to analyze podocyte developmental defects, such as those observed in congenital nephrotic syndrome, and can be taken in consideration for pharmacological studies of severe early podocyte injury.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping