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Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning
The renal stroma is an embryonic cell population located in the cortex that provides a structural framework as well as a source of endothelial progenitors for the developing kidney. The exact role of the renal stroma in normal kidney development hasn't been clearly defined. However, previous st...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914987/ https://www.ncbi.nlm.nih.gov/pubmed/24505489 http://dx.doi.org/10.1371/journal.pone.0088400 |
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author | Hum, Stephanie Rymer, Christopher Schaefer, Caitlin Bushnell, Daniel Sims-Lucas, Sunder |
author_facet | Hum, Stephanie Rymer, Christopher Schaefer, Caitlin Bushnell, Daniel Sims-Lucas, Sunder |
author_sort | Hum, Stephanie |
collection | PubMed |
description | The renal stroma is an embryonic cell population located in the cortex that provides a structural framework as well as a source of endothelial progenitors for the developing kidney. The exact role of the renal stroma in normal kidney development hasn't been clearly defined. However, previous studies have shown that the genetic deletion of Foxd1, a renal stroma specific gene, leads to severe kidney malformations confirming the importance of stroma in normal kidney development. This study further investigates the role of renal stroma by ablating Foxd1-derived stroma cells themselves and observing the response of the remaining cell populations. A Foxd1cre (renal stroma specific) mouse was crossed with a diphtheria toxin mouse (DTA) to specifically induce apoptosis in stromal cells. Histological examination of kidneys at embryonic day 13.5–18.5 showed a lack of stromal tissue, mispatterning of renal structures, and dysplastic and/or fused horseshoe kidneys. Immunofluorescence staining of nephron progenitors, vasculature, ureteric epithelium, differentiated nephron progenitors, and vascular supportive cells revealed that mutants had thickened nephron progenitor caps, cortical regions devoid of nephron progenitors, aberrant vessel patterning and thickening, ureteric branching defects and migration of differentiated nephron structures into the medulla. The similarities between the renal deformities caused by Foxd1 genetic knockout and Foxd1DTA mouse models reveal the importance of Foxd1 in mediating and maintaining the functional integrity of the renal stroma. |
format | Online Article Text |
id | pubmed-3914987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39149872014-02-06 Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning Hum, Stephanie Rymer, Christopher Schaefer, Caitlin Bushnell, Daniel Sims-Lucas, Sunder PLoS One Research Article The renal stroma is an embryonic cell population located in the cortex that provides a structural framework as well as a source of endothelial progenitors for the developing kidney. The exact role of the renal stroma in normal kidney development hasn't been clearly defined. However, previous studies have shown that the genetic deletion of Foxd1, a renal stroma specific gene, leads to severe kidney malformations confirming the importance of stroma in normal kidney development. This study further investigates the role of renal stroma by ablating Foxd1-derived stroma cells themselves and observing the response of the remaining cell populations. A Foxd1cre (renal stroma specific) mouse was crossed with a diphtheria toxin mouse (DTA) to specifically induce apoptosis in stromal cells. Histological examination of kidneys at embryonic day 13.5–18.5 showed a lack of stromal tissue, mispatterning of renal structures, and dysplastic and/or fused horseshoe kidneys. Immunofluorescence staining of nephron progenitors, vasculature, ureteric epithelium, differentiated nephron progenitors, and vascular supportive cells revealed that mutants had thickened nephron progenitor caps, cortical regions devoid of nephron progenitors, aberrant vessel patterning and thickening, ureteric branching defects and migration of differentiated nephron structures into the medulla. The similarities between the renal deformities caused by Foxd1 genetic knockout and Foxd1DTA mouse models reveal the importance of Foxd1 in mediating and maintaining the functional integrity of the renal stroma. Public Library of Science 2014-02-05 /pmc/articles/PMC3914987/ /pubmed/24505489 http://dx.doi.org/10.1371/journal.pone.0088400 Text en © 2014 Hum 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 Hum, Stephanie Rymer, Christopher Schaefer, Caitlin Bushnell, Daniel Sims-Lucas, Sunder Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning |
title | Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning |
title_full | Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning |
title_fullStr | Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning |
title_full_unstemmed | Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning |
title_short | Ablation of the Renal Stroma Defines Its Critical Role in Nephron Progenitor and Vasculature Patterning |
title_sort | ablation of the renal stroma defines its critical role in nephron progenitor and vasculature patterning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914987/ https://www.ncbi.nlm.nih.gov/pubmed/24505489 http://dx.doi.org/10.1371/journal.pone.0088400 |
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