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Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron

The different segments of the nephron and glomerulus in the kidney balance the processes of water homeostasis, solute recovery, blood filtration, and metabolite excretion. When segment function is disrupted, a range of pathological features are presented. Little is known about nephron patterning dur...

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Autores principales: Lindström, Nils O, Lawrence, Melanie L, Burn, Sally F, Johansson, Jeanette A, Bakker, Elvira RM, Ridgway, Rachel A, Chang, C-Hong, Karolak, Michele J, Oxburgh, Leif, Headon, Denis J, Sansom, Owen J, Smits, Ron, Davies, Jamie A, Hohenstein, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337611/
https://www.ncbi.nlm.nih.gov/pubmed/25647637
http://dx.doi.org/10.7554/eLife.04000
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author Lindström, Nils O
Lawrence, Melanie L
Burn, Sally F
Johansson, Jeanette A
Bakker, Elvira RM
Ridgway, Rachel A
Chang, C-Hong
Karolak, Michele J
Oxburgh, Leif
Headon, Denis J
Sansom, Owen J
Smits, Ron
Davies, Jamie A
Hohenstein, Peter
author_facet Lindström, Nils O
Lawrence, Melanie L
Burn, Sally F
Johansson, Jeanette A
Bakker, Elvira RM
Ridgway, Rachel A
Chang, C-Hong
Karolak, Michele J
Oxburgh, Leif
Headon, Denis J
Sansom, Owen J
Smits, Ron
Davies, Jamie A
Hohenstein, Peter
author_sort Lindström, Nils O
collection PubMed
description The different segments of the nephron and glomerulus in the kidney balance the processes of water homeostasis, solute recovery, blood filtration, and metabolite excretion. When segment function is disrupted, a range of pathological features are presented. Little is known about nephron patterning during embryogenesis. In this study, we demonstrate that the early nephron is patterned by a gradient in β-catenin activity along the axis of the nephron tubule. By modifying β-catenin activity, we force cells within nephrons to differentiate according to the imposed β-catenin activity level, thereby causing spatial shifts in nephron segments. The β-catenin signalling gradient interacts with the BMP pathway which, through PTEN/PI3K/AKT signalling, antagonises β-catenin activity and promotes segment identities associated with low β-catenin activity. β-catenin activity and PI3K signalling also integrate with Notch signalling to control segmentation: modulating β-catenin activity or PI3K rescues segment identities normally lost by inhibition of Notch. Our data therefore identifies a molecular network for nephron patterning. DOI: http://dx.doi.org/10.7554/eLife.04000.001
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spelling pubmed-43376112015-03-04 Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron Lindström, Nils O Lawrence, Melanie L Burn, Sally F Johansson, Jeanette A Bakker, Elvira RM Ridgway, Rachel A Chang, C-Hong Karolak, Michele J Oxburgh, Leif Headon, Denis J Sansom, Owen J Smits, Ron Davies, Jamie A Hohenstein, Peter eLife Developmental Biology and Stem Cells The different segments of the nephron and glomerulus in the kidney balance the processes of water homeostasis, solute recovery, blood filtration, and metabolite excretion. When segment function is disrupted, a range of pathological features are presented. Little is known about nephron patterning during embryogenesis. In this study, we demonstrate that the early nephron is patterned by a gradient in β-catenin activity along the axis of the nephron tubule. By modifying β-catenin activity, we force cells within nephrons to differentiate according to the imposed β-catenin activity level, thereby causing spatial shifts in nephron segments. The β-catenin signalling gradient interacts with the BMP pathway which, through PTEN/PI3K/AKT signalling, antagonises β-catenin activity and promotes segment identities associated with low β-catenin activity. β-catenin activity and PI3K signalling also integrate with Notch signalling to control segmentation: modulating β-catenin activity or PI3K rescues segment identities normally lost by inhibition of Notch. Our data therefore identifies a molecular network for nephron patterning. DOI: http://dx.doi.org/10.7554/eLife.04000.001 eLife Sciences Publications, Ltd 2015-02-03 /pmc/articles/PMC4337611/ /pubmed/25647637 http://dx.doi.org/10.7554/eLife.04000 Text en © 2014, Lindström et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology and Stem Cells
Lindström, Nils O
Lawrence, Melanie L
Burn, Sally F
Johansson, Jeanette A
Bakker, Elvira RM
Ridgway, Rachel A
Chang, C-Hong
Karolak, Michele J
Oxburgh, Leif
Headon, Denis J
Sansom, Owen J
Smits, Ron
Davies, Jamie A
Hohenstein, Peter
Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron
title Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron
title_full Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron
title_fullStr Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron
title_full_unstemmed Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron
title_short Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron
title_sort integrated β-catenin, bmp, pten, and notch signalling patterns the nephron
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337611/
https://www.ncbi.nlm.nih.gov/pubmed/25647637
http://dx.doi.org/10.7554/eLife.04000
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