Literature DB >> 28409342

Zebrafish as a Model of Kidney Disease.

Elvin E Morales1, Rebecca A Wingert2.   

Abstract

Animal models have been an invaluable means to advance biomedical research as they provide experimental avenues for cellular and molecular investigations of disease pathology. The zebrafish (Danio rerio) is a good alternative to mammalian models that can be used to apply powerful genetic experimental methods normally used in invertebrates to answer questions about vertebrate development and disease. In the case of the kidney, the zebrafish has proven itself to be an applicable and versatile experimental system, mainly due to the simplicity of its pronephros, which contains two nephrons that possess conserved structural and physiological aspects with mammalian nephrons. Numerous genes that were not previously related to kidney conditions have now been linked to renal diseases by applying genetic screening with the zebrafish. In fact, a large collection of mutations that affect nephron formation and function were generated through phenotype-based forward screens. Complementary reverse genetic approaches have also been insightful, with methods spanning the use of antisense morpholino oligonucleotides to genome editing approaches such as the CRISPR/Cas9 system, to selectively knock down or knock out genes of interest to see if they produce kidney phenotypes. Acute kidney injury (AKI) has also been easily modeled in the zebrafish by injecting nephrotoxins, directly inducing damage through surgical intervention, or by generating transgenic lines that express compounds in a tissue-specific manner that when exposed to certain drugs promote an apoptotic response within cells. In this chapter, we provide an overview of these various approaches as well as discuss many of the contributions that have been achieved through the use of zebrafish to model kidney disease.

Entities:  

Mesh:

Year:  2017        PMID: 28409342     DOI: 10.1007/978-3-319-51436-9_3

Source DB:  PubMed          Journal:  Results Probl Cell Differ        ISSN: 0080-1844


  14 in total

Review 1.  Mechanisms of Nephrogenesis Revealed by Zebrafish Chemical Screen: Prostaglandin Signaling Modulates Nephron Progenitor Fate.

Authors:  Brooke E Chambers; Rebecca A Wingert
Journal:  Nephron       Date:  2019-06-19       Impact factor: 2.847

2.  The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros development.

Authors:  Paul T Kroeger; Bridgette E Drummond; Rachel Miceli; Michael McKernan; Gary F Gerlach; Amanda N Marra; Annemarie Fox; Kristen K McCampbell; Ignaty Leshchiner; Adriana Rodriguez-Mari; Ruth BreMiller; Ryan Thummel; Alan J Davidson; John Postlethwait; Wolfram Goessling; Rebecca A Wingert
Journal:  Dev Biol       Date:  2017-06-01       Impact factor: 3.582

Review 3.  Insights Gained From Zebrafish Models for the Ciliopathy Joubert Syndrome.

Authors:  Tamara D S Rusterholz; Claudia Hofmann; Ruxandra Bachmann-Gagescu
Journal:  Front Genet       Date:  2022-06-30       Impact factor: 4.772

4.  Dissecting hematopoietic and renal cell heterogeneity in adult zebrafish at single-cell resolution using RNA sequencing.

Authors:  Qin Tang; Sowmya Iyer; Riadh Lobbardi; John C Moore; Huidong Chen; Caleb Lareau; Christine Hebert; McKenzie L Shaw; Cyril Neftel; Mario L Suva; Craig J Ceol; Andre Bernards; Martin Aryee; Luca Pinello; Iain A Drummond; David M Langenau
Journal:  J Exp Med       Date:  2017-09-06       Impact factor: 14.307

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

Authors:  Petrus J Steenbergen; Jana Heigwer; Gunjan Pandey; Burkhard Tönshoff; Jochen Gehrig; Jens H Westhoff
Journal:  Cells       Date:  2020-05-20       Impact factor: 6.600

6.  Homeogene emx1 is required for nephron distal segment development in zebrafish.

Authors:  Elvin E Morales; Nicole Handa; Bridgette E Drummond; Joseph M Chambers; Amanda N Marra; Amanda Addiego; Rebecca A Wingert
Journal:  Sci Rep       Date:  2018-12-21       Impact factor: 4.379

7.  Moderate Nucleoporin 133 deficiency leads to glomerular damage in zebrafish.

Authors:  Chiara Cianciolo Cosentino; Alessandro Berto; Stéphane Pelletier; Michelle Hari; Johannes Loffing; Stephan C F Neuhauss; Valérie Doye
Journal:  Sci Rep       Date:  2019-03-18       Impact factor: 4.379

8.  Iroquois transcription factor irx2a is required for multiciliated and transporter cell fate decisions during zebrafish pronephros development.

Authors:  Amanda N Marra; Christina N Cheng; Basma Adeeb; Amanda Addiego; Hannah M Wesselman; Brooke E Chambers; Joseph M Chambers; Rebecca A Wingert
Journal:  Sci Rep       Date:  2019-04-23       Impact factor: 4.379

9.  The SARS-CoV-2 receptor and other key components of the Renin-Angiotensin-Aldosterone System related to COVID-19 are expressed in enterocytes in larval zebrafish.

Authors:  John H Postlethwait; Michelle S Massaquoi; Dylan R Farnsworth; Yi-Lin Yan; Karen Guillemin; Adam C Miller
Journal:  Biol Open       Date:  2021-03-23       Impact factor: 2.643

Review 10.  Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases.

Authors:  Jochen Gehrig; Gunjan Pandey; Jens H Westhoff
Journal:  Front Pediatr       Date:  2018-06-28       Impact factor: 3.418

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