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Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct

Pronephros, a developmental model for adult mammalian kidneys (metanephros) and a functional kidney in early teleosts, consists of glomerulus, tubule, and duct. These structural and functional elements are responsible for different kidney functions, e.g., blood filtration, waste extraction, salt rec...

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Detalles Bibliográficos
Autores principales: Ma, Ming, Jiang, Yun-Jin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781496/
https://www.ncbi.nlm.nih.gov/pubmed/17257056
http://dx.doi.org/10.1371/journal.pgen.0030018
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author Ma, Ming
Jiang, Yun-Jin
author_facet Ma, Ming
Jiang, Yun-Jin
author_sort Ma, Ming
collection PubMed
description Pronephros, a developmental model for adult mammalian kidneys (metanephros) and a functional kidney in early teleosts, consists of glomerulus, tubule, and duct. These structural and functional elements are responsible for different kidney functions, e.g., blood filtration, waste extraction, salt recovery, and water balance. During pronephros organogenesis, cell differentiation is a key step in generating different cell types in specific locations to accomplish designated functions. However, it is poorly understood what molecules regulate the differentiation of different cell types in different parts of the kidney. Two types of epithelial cells, multi-cilia cells and principal cells, are found in the epithelia of the zebrafish distal pronephric duct. While the former is characterized by at least 15 apically localized cilia and expresses centrin2 and rfx2, the latter is characterized by a single primary cilium and sodium pumps. Multi-cilia cells and principal cells differentiate from 17.5 hours post-fertilization onwards in a mosaic pattern. Jagged2a-Notch1a/Notch3-Her9 is responsible for specification and patterning of these two cell types through a lateral inhibition mechanism. Furthermore, multi-cilia cell hyperplasia was observed in mind bomb mutants and Mind bomb was shown to interact with Jagged2a and facilitate its internalization. Taken together, our findings add a new paradigm of Notch signaling in kidney development, namely, that Jagged2a-Notch signaling modulates cell fate choice in a nephric segment, the distal pronephric duct.
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spelling pubmed-17814962007-01-25 Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct Ma, Ming Jiang, Yun-Jin PLoS Genet Research Article Pronephros, a developmental model for adult mammalian kidneys (metanephros) and a functional kidney in early teleosts, consists of glomerulus, tubule, and duct. These structural and functional elements are responsible for different kidney functions, e.g., blood filtration, waste extraction, salt recovery, and water balance. During pronephros organogenesis, cell differentiation is a key step in generating different cell types in specific locations to accomplish designated functions. However, it is poorly understood what molecules regulate the differentiation of different cell types in different parts of the kidney. Two types of epithelial cells, multi-cilia cells and principal cells, are found in the epithelia of the zebrafish distal pronephric duct. While the former is characterized by at least 15 apically localized cilia and expresses centrin2 and rfx2, the latter is characterized by a single primary cilium and sodium pumps. Multi-cilia cells and principal cells differentiate from 17.5 hours post-fertilization onwards in a mosaic pattern. Jagged2a-Notch1a/Notch3-Her9 is responsible for specification and patterning of these two cell types through a lateral inhibition mechanism. Furthermore, multi-cilia cell hyperplasia was observed in mind bomb mutants and Mind bomb was shown to interact with Jagged2a and facilitate its internalization. Taken together, our findings add a new paradigm of Notch signaling in kidney development, namely, that Jagged2a-Notch signaling modulates cell fate choice in a nephric segment, the distal pronephric duct. Public Library of Science 2007-01 2007-01-26 /pmc/articles/PMC1781496/ /pubmed/17257056 http://dx.doi.org/10.1371/journal.pgen.0030018 Text en © 2007 Ma and Jiang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ma, Ming
Jiang, Yun-Jin
Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct
title Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct
title_full Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct
title_fullStr Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct
title_full_unstemmed Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct
title_short Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct
title_sort jagged2a-notch signaling mediates cell fate choice in the zebrafish pronephric duct
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781496/
https://www.ncbi.nlm.nih.gov/pubmed/17257056
http://dx.doi.org/10.1371/journal.pgen.0030018
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