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Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney

The zebrafish model has emerged as a relevant system to study kidney development, regeneration and disease. Both the embryonic and adult zebrafish kidneys are composed of functional units known as nephrons, which are highly conserved with other vertebrates, including mammals. Research in zebrafish h...

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Autores principales: McCampbell, Kristen K., Springer, Kristin N., Wingert, Rebecca A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459603/
https://www.ncbi.nlm.nih.gov/pubmed/25145398
http://dx.doi.org/10.3791/51644
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author McCampbell, Kristen K.
Springer, Kristin N.
Wingert, Rebecca A.
author_facet McCampbell, Kristen K.
Springer, Kristin N.
Wingert, Rebecca A.
author_sort McCampbell, Kristen K.
collection PubMed
description The zebrafish model has emerged as a relevant system to study kidney development, regeneration and disease. Both the embryonic and adult zebrafish kidneys are composed of functional units known as nephrons, which are highly conserved with other vertebrates, including mammals. Research in zebrafish has recently demonstrated that two distinctive phenomena transpire after adult nephrons incur damage: first, there is robust regeneration within existing nephrons that replaces the destroyed tubule epithelial cells; second, entirely new nephrons are produced from renal progenitors in a process known as neonephrogenesis. In contrast, humans and other mammals seem to have only a limited ability for nephron epithelial regeneration. To date, the mechanisms responsible for these kidney regeneration phenomena remain poorly understood. Since adult zebrafish kidneys undergo both nephron epithelial regeneration and neonephrogenesis, they provide an outstanding experimental paradigm to study these events. Further, there is a wide range of genetic and pharmacological tools available in the zebrafish model that can be used to delineate the cellular and molecular mechanisms that regulate renal regeneration. One essential aspect of such research is the evaluation of nephron structure and function. This protocol describes a set of labeling techniques that can be used to gauge renal composition and test nephron functionality in the adult zebrafish kidney. Thus, these methods are widely applicable to the future phenotypic characterization of adult zebrafish kidney injury paradigms, which include but are not limited to, nephrotoxicant exposure regimes or genetic methods of targeted cell death such as the nitroreductase mediated cell ablation technique. Further, these methods could be used to study genetic perturbations in adult kidney formation and could also be applied to assess renal status during chronic disease modeling.
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spelling pubmed-44596032015-06-08 Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney McCampbell, Kristen K. Springer, Kristin N. Wingert, Rebecca A. J Vis Exp Cellular Biology The zebrafish model has emerged as a relevant system to study kidney development, regeneration and disease. Both the embryonic and adult zebrafish kidneys are composed of functional units known as nephrons, which are highly conserved with other vertebrates, including mammals. Research in zebrafish has recently demonstrated that two distinctive phenomena transpire after adult nephrons incur damage: first, there is robust regeneration within existing nephrons that replaces the destroyed tubule epithelial cells; second, entirely new nephrons are produced from renal progenitors in a process known as neonephrogenesis. In contrast, humans and other mammals seem to have only a limited ability for nephron epithelial regeneration. To date, the mechanisms responsible for these kidney regeneration phenomena remain poorly understood. Since adult zebrafish kidneys undergo both nephron epithelial regeneration and neonephrogenesis, they provide an outstanding experimental paradigm to study these events. Further, there is a wide range of genetic and pharmacological tools available in the zebrafish model that can be used to delineate the cellular and molecular mechanisms that regulate renal regeneration. One essential aspect of such research is the evaluation of nephron structure and function. This protocol describes a set of labeling techniques that can be used to gauge renal composition and test nephron functionality in the adult zebrafish kidney. Thus, these methods are widely applicable to the future phenotypic characterization of adult zebrafish kidney injury paradigms, which include but are not limited to, nephrotoxicant exposure regimes or genetic methods of targeted cell death such as the nitroreductase mediated cell ablation technique. Further, these methods could be used to study genetic perturbations in adult kidney formation and could also be applied to assess renal status during chronic disease modeling. MyJove Corporation 2014-08-09 /pmc/articles/PMC4459603/ /pubmed/25145398 http://dx.doi.org/10.3791/51644 Text en Copyright © 2014, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Cellular Biology
McCampbell, Kristen K.
Springer, Kristin N.
Wingert, Rebecca A.
Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
title Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
title_full Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
title_fullStr Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
title_full_unstemmed Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
title_short Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
title_sort analysis of nephron composition and function in the adult zebrafish kidney
topic Cellular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459603/
https://www.ncbi.nlm.nih.gov/pubmed/25145398
http://dx.doi.org/10.3791/51644
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