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Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney

BACKGROUND: While kidney injury is associated with re-expression of numerous Wnt ligands and receptors, molecular mechanisms which underlie regulation of distinct Wnt signaling pathways and ensuing biological consequences remain incompletely understood. Primary cilia are increasingly being recognize...

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Autores principales: Saito, Shoji, Tampe, Björn, Müller, Gerhard A, Zeisberg, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404279/
https://www.ncbi.nlm.nih.gov/pubmed/25901180
http://dx.doi.org/10.1186/s13069-015-0024-y
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author Saito, Shoji
Tampe, Björn
Müller, Gerhard A
Zeisberg, Michael
author_facet Saito, Shoji
Tampe, Björn
Müller, Gerhard A
Zeisberg, Michael
author_sort Saito, Shoji
collection PubMed
description BACKGROUND: While kidney injury is associated with re-expression of numerous Wnt ligands and receptors, molecular mechanisms which underlie regulation of distinct Wnt signaling pathways and ensuing biological consequences remain incompletely understood. Primary cilia are increasingly being recognized as cellular ‘antennae’ which sense and transduce signals from the microenvironment, particularly through Wnt signaling. Here, we explored the role of cilia as modulators of canonical and non-canonical Wnt signaling activities involving tubular epithelial cells in the injured kidney. RESULTS: We demonstrate that in the mouse model of unilateral ureter obstruction, progression of kidney injury correlates with increased expression of numerous Wnt ligands, and that increased expression of Wnt ligands corresponded with over-activation of canonical Wnt signaling. In contrast, non-canonical Wnt signaling dropped significantly during the course of kidney injury despite gradually increased expression of typical non-canonical and intermediate Wnt signaling ligands. We further demonstrate that in cultured tubular epithelial cells, cilia modulate balance between canonical and non-canonical signaling responses upon exposure to Wnt ligands. CONCLUSIONS: We provide evidence that in the context of renal injury, primary cilia act as molecular switches between canonical and non-canonical Wnt signaling activity, possibly determining between regenerative and pro-fibrotic effects of Wnt re-expression in the injured kidney. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13069-015-0024-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-44042792015-04-22 Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney Saito, Shoji Tampe, Björn Müller, Gerhard A Zeisberg, Michael Fibrogenesis Tissue Repair Research BACKGROUND: While kidney injury is associated with re-expression of numerous Wnt ligands and receptors, molecular mechanisms which underlie regulation of distinct Wnt signaling pathways and ensuing biological consequences remain incompletely understood. Primary cilia are increasingly being recognized as cellular ‘antennae’ which sense and transduce signals from the microenvironment, particularly through Wnt signaling. Here, we explored the role of cilia as modulators of canonical and non-canonical Wnt signaling activities involving tubular epithelial cells in the injured kidney. RESULTS: We demonstrate that in the mouse model of unilateral ureter obstruction, progression of kidney injury correlates with increased expression of numerous Wnt ligands, and that increased expression of Wnt ligands corresponded with over-activation of canonical Wnt signaling. In contrast, non-canonical Wnt signaling dropped significantly during the course of kidney injury despite gradually increased expression of typical non-canonical and intermediate Wnt signaling ligands. We further demonstrate that in cultured tubular epithelial cells, cilia modulate balance between canonical and non-canonical signaling responses upon exposure to Wnt ligands. CONCLUSIONS: We provide evidence that in the context of renal injury, primary cilia act as molecular switches between canonical and non-canonical Wnt signaling activity, possibly determining between regenerative and pro-fibrotic effects of Wnt re-expression in the injured kidney. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13069-015-0024-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-16 /pmc/articles/PMC4404279/ /pubmed/25901180 http://dx.doi.org/10.1186/s13069-015-0024-y Text en © Saito et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Saito, Shoji
Tampe, Björn
Müller, Gerhard A
Zeisberg, Michael
Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney
title Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney
title_full Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney
title_fullStr Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney
title_full_unstemmed Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney
title_short Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney
title_sort primary cilia modulate balance of canonical and non-canonical wnt signaling responses in the injured kidney
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404279/
https://www.ncbi.nlm.nih.gov/pubmed/25901180
http://dx.doi.org/10.1186/s13069-015-0024-y
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