Literature DB >> 31493818

Visualizing gene expression during zebrafish pronephros development and regeneration.

Amanda N Marra1, Brooke E Chambers1, Joseph M Chambers1, Bridgette E Drummond1, Basma D Adeeb1, Hannah M Wesselman1, Elvin E Morales1, Nicole Handa1, Tom Pettini2, Matthew Ronshaugen2, Rebecca A Wingert3.   

Abstract

The vertebrate kidney is comprised of functional units known as nephrons. Defects in nephron development or activity are a common feature of kidney disease. Current medical treatments are unable to ameliorate the dire consequences of nephron deficit or injury. Although there have been tremendous advancements in our understanding of nephron ontogeny and the response to damage, many significant knowledge gaps still remain. The zebrafish embryo kidney, or pronephros, is an ideal model for many renal development and regeneration studies because it is comprised of nephrons that share conserved features with the nephron units that comprise the mammalian metanephric kidney. In this chapter, we provide an overview about the benefits of using the zebrafish pronephros to study the mechanisms underlying nephrogenesis as well as epithelial repair and regeneration. We subsequently detail methods for the spatiotemporal assessment of gene and protein expression in zebrafish embryos that can be used to extend the understanding of nephron development and disease, and thereby create new opportunities to identify therapeutic strategies for regenerative medicine.
© 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Kidney; Nephrogenesis; Nephron; Pronephros; Regeneration; Segment; Zebrafish

Mesh:

Substances:

Year:  2019        PMID: 31493818     DOI: 10.1016/bs.mcb.2019.06.003

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  3 in total

1.  Dynamic properties of noise and Her6 levels are optimized by miR-9, allowing the decoding of the Her6 oscillator.

Authors:  Ximena Soto; Veronica Biga; Jochen Kursawe; Robert Lea; Parnian Doostdar; Riba Thomas; Nancy Papalopulu
Journal:  EMBO J       Date:  2020-05-12       Impact factor: 11.598

2.  Ppargc1a Controls Ciliated Cell Development by Regulating Prostaglandin Biosynthesis.

Authors:  Joseph M Chambers; Amanda Addiego; Ana L Flores-Mireles; Rebecca A Wingert
Journal:  Cell Rep       Date:  2020-11-10       Impact factor: 9.423

3.  Kctd15 regulates nephron segment development by repressing Tfap2a activity.

Authors:  Brooke E Chambers; Eleanor G Clark; Allison E Gatz; Rebecca A Wingert
Journal:  Development       Date:  2020-12-14       Impact factor: 6.862

  3 in total

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