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Collective Cell Migration Drives Morphogenesis of the Kidney Nephron
Tissue organization in epithelial organs is achieved during development by the combined processes of cell differentiation and morphogenetic cell movements. In the kidney, the nephron is the functional organ unit. Each nephron is an epithelial tubule that is subdivided into discrete segments with spe...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613420/ https://www.ncbi.nlm.nih.gov/pubmed/19127979 http://dx.doi.org/10.1371/journal.pbio.1000009 |
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author | Vasilyev, Aleksandr Liu, Yan Mudumana, Sudha Mangos, Steve Lam, Pui-Ying Majumdar, Arindam Zhao, Jinhua Poon, Kar-Lai Kondrychyn, Igor Korzh, Vladimir Drummond, Iain A |
author_facet | Vasilyev, Aleksandr Liu, Yan Mudumana, Sudha Mangos, Steve Lam, Pui-Ying Majumdar, Arindam Zhao, Jinhua Poon, Kar-Lai Kondrychyn, Igor Korzh, Vladimir Drummond, Iain A |
author_sort | Vasilyev, Aleksandr |
collection | PubMed |
description | Tissue organization in epithelial organs is achieved during development by the combined processes of cell differentiation and morphogenetic cell movements. In the kidney, the nephron is the functional organ unit. Each nephron is an epithelial tubule that is subdivided into discrete segments with specific transport functions. Little is known about how nephron segments are defined or how segments acquire their distinctive morphology and cell shape. Using live, in vivo cell imaging of the forming zebrafish pronephric nephron, we found that the migration of fully differentiated epithelial cells accounts for both the final position of nephron segment boundaries and the characteristic convolution of the proximal tubule. Pronephric cells maintain adherens junctions and polarized apical brush border membranes while they migrate collectively. Individual tubule cells exhibit basal membrane protrusions in the direction of movement and appear to establish transient, phosphorylated Focal Adhesion Kinase–positive adhesions to the basement membrane. Cell migration continued in the presence of camptothecin, indicating that cell division does not drive migration. Lengthening of the nephron was, however, accompanied by an increase in tubule cell number, specifically in the most distal, ret1-positive nephron segment. The initiation of cell migration coincided with the onset of fluid flow in the pronephros. Complete blockade of pronephric fluid flow prevented cell migration and proximal nephron convolution. Selective blockade of proximal, filtration-driven fluid flow shifted the position of tubule convolution distally and revealed a role for cilia-driven fluid flow in persistent migration of distal nephron cells. We conclude that nephron morphogenesis is driven by fluid flow–dependent, collective epithelial cell migration within the confines of the tubule basement membrane. Our results establish intimate links between nephron function, fluid flow, and morphogenesis. |
format | Text |
id | pubmed-2613420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26134202009-01-06 Collective Cell Migration Drives Morphogenesis of the Kidney Nephron Vasilyev, Aleksandr Liu, Yan Mudumana, Sudha Mangos, Steve Lam, Pui-Ying Majumdar, Arindam Zhao, Jinhua Poon, Kar-Lai Kondrychyn, Igor Korzh, Vladimir Drummond, Iain A PLoS Biol Research Article Tissue organization in epithelial organs is achieved during development by the combined processes of cell differentiation and morphogenetic cell movements. In the kidney, the nephron is the functional organ unit. Each nephron is an epithelial tubule that is subdivided into discrete segments with specific transport functions. Little is known about how nephron segments are defined or how segments acquire their distinctive morphology and cell shape. Using live, in vivo cell imaging of the forming zebrafish pronephric nephron, we found that the migration of fully differentiated epithelial cells accounts for both the final position of nephron segment boundaries and the characteristic convolution of the proximal tubule. Pronephric cells maintain adherens junctions and polarized apical brush border membranes while they migrate collectively. Individual tubule cells exhibit basal membrane protrusions in the direction of movement and appear to establish transient, phosphorylated Focal Adhesion Kinase–positive adhesions to the basement membrane. Cell migration continued in the presence of camptothecin, indicating that cell division does not drive migration. Lengthening of the nephron was, however, accompanied by an increase in tubule cell number, specifically in the most distal, ret1-positive nephron segment. The initiation of cell migration coincided with the onset of fluid flow in the pronephros. Complete blockade of pronephric fluid flow prevented cell migration and proximal nephron convolution. Selective blockade of proximal, filtration-driven fluid flow shifted the position of tubule convolution distally and revealed a role for cilia-driven fluid flow in persistent migration of distal nephron cells. We conclude that nephron morphogenesis is driven by fluid flow–dependent, collective epithelial cell migration within the confines of the tubule basement membrane. Our results establish intimate links between nephron function, fluid flow, and morphogenesis. Public Library of Science 2009-01 2009-01-06 /pmc/articles/PMC2613420/ /pubmed/19127979 http://dx.doi.org/10.1371/journal.pbio.1000009 Text en © 2009 Vasilyev et al. 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 Vasilyev, Aleksandr Liu, Yan Mudumana, Sudha Mangos, Steve Lam, Pui-Ying Majumdar, Arindam Zhao, Jinhua Poon, Kar-Lai Kondrychyn, Igor Korzh, Vladimir Drummond, Iain A Collective Cell Migration Drives Morphogenesis of the Kidney Nephron |
title | Collective Cell Migration Drives Morphogenesis of the Kidney Nephron |
title_full | Collective Cell Migration Drives Morphogenesis of the Kidney Nephron |
title_fullStr | Collective Cell Migration Drives Morphogenesis of the Kidney Nephron |
title_full_unstemmed | Collective Cell Migration Drives Morphogenesis of the Kidney Nephron |
title_short | Collective Cell Migration Drives Morphogenesis of the Kidney Nephron |
title_sort | collective cell migration drives morphogenesis of the kidney nephron |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613420/ https://www.ncbi.nlm.nih.gov/pubmed/19127979 http://dx.doi.org/10.1371/journal.pbio.1000009 |
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