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A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development

The epithelial ureteric bud is critical for mammalian kidney development as it generates the ureter and the collecting duct system that induces nephrogenesis in dicrete locations in the kidney mesenchyme during its emergence. We show that a secreted Bmp antagonist Cerberus homologue (Cer1) fine tune...

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Autores principales: Chi, Lijun, Saarela, Ulla, Railo, Antti, Prunskaite-Hyyryläinen, Renata, Skovorodkin, Ilya, Anthony, Shelagh, Katsu, Kenjiro, Liu, Yu, Shan, Jingdong, Salgueiro, Ana Marisa, Belo, José António, Davies, Jamie, Yokouchi, Yuji, Vainio, Seppo J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219680/
https://www.ncbi.nlm.nih.gov/pubmed/22114682
http://dx.doi.org/10.1371/journal.pone.0027676
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author Chi, Lijun
Saarela, Ulla
Railo, Antti
Prunskaite-Hyyryläinen, Renata
Skovorodkin, Ilya
Anthony, Shelagh
Katsu, Kenjiro
Liu, Yu
Shan, Jingdong
Salgueiro, Ana Marisa
Belo, José António
Davies, Jamie
Yokouchi, Yuji
Vainio, Seppo J.
author_facet Chi, Lijun
Saarela, Ulla
Railo, Antti
Prunskaite-Hyyryläinen, Renata
Skovorodkin, Ilya
Anthony, Shelagh
Katsu, Kenjiro
Liu, Yu
Shan, Jingdong
Salgueiro, Ana Marisa
Belo, José António
Davies, Jamie
Yokouchi, Yuji
Vainio, Seppo J.
author_sort Chi, Lijun
collection PubMed
description The epithelial ureteric bud is critical for mammalian kidney development as it generates the ureter and the collecting duct system that induces nephrogenesis in dicrete locations in the kidney mesenchyme during its emergence. We show that a secreted Bmp antagonist Cerberus homologue (Cer1) fine tunes the organization of the ureteric tree during organogenesis in the mouse embryo. Both enhanced ureteric expression of Cer1 and Cer1 knock out enlarge kidney size, and these changes are associated with an altered three-dimensional structure of the ureteric tree as revealed by optical projection tomography. Enhanced Cer1 expression changes the ureteric bud branching programme so that more trifid and lateral branches rather than bifid ones develop, as seen in time-lapse organ culture. These changes may be the reasons for the modified spatial arrangement of the ureteric tree in the kidneys of Cer1+ embryos. Cer1 gain of function is associated with moderately elevated expression of Gdnf and Wnt11, which is also induced in the case of Cer1 deficiency, where Bmp4 expression is reduced, indicating the dependence of Bmp expression on Cer1. Cer1 binds at least Bmp2/4 and antagonizes Bmp signalling in cell culture. In line with this, supplementation of Bmp4 restored the ureteric bud tip number, which was reduced by Cer1+ to bring it closer to the normal, consistent with models suggesting that Bmp signalling inhibits ureteric bud development. Genetic reduction of Wnt11 inhibited the Cer1-stimulated kidney development, but Cer1 did not influence Wnt11 signalling in cell culture, although it did inhibit the Wnt3a-induced canonical Top Flash reporter to some extent. We conclude that Cer1 fine tunes the spatial organization of the ureteric tree by coordinating the activities of the growth-promoting ureteric bud signals Gndf and Wnt11 via Bmp-mediated antagonism and to some degree via the canonical Wnt signalling involved in branching.
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spelling pubmed-32196802011-11-23 A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development Chi, Lijun Saarela, Ulla Railo, Antti Prunskaite-Hyyryläinen, Renata Skovorodkin, Ilya Anthony, Shelagh Katsu, Kenjiro Liu, Yu Shan, Jingdong Salgueiro, Ana Marisa Belo, José António Davies, Jamie Yokouchi, Yuji Vainio, Seppo J. PLoS One Research Article The epithelial ureteric bud is critical for mammalian kidney development as it generates the ureter and the collecting duct system that induces nephrogenesis in dicrete locations in the kidney mesenchyme during its emergence. We show that a secreted Bmp antagonist Cerberus homologue (Cer1) fine tunes the organization of the ureteric tree during organogenesis in the mouse embryo. Both enhanced ureteric expression of Cer1 and Cer1 knock out enlarge kidney size, and these changes are associated with an altered three-dimensional structure of the ureteric tree as revealed by optical projection tomography. Enhanced Cer1 expression changes the ureteric bud branching programme so that more trifid and lateral branches rather than bifid ones develop, as seen in time-lapse organ culture. These changes may be the reasons for the modified spatial arrangement of the ureteric tree in the kidneys of Cer1+ embryos. Cer1 gain of function is associated with moderately elevated expression of Gdnf and Wnt11, which is also induced in the case of Cer1 deficiency, where Bmp4 expression is reduced, indicating the dependence of Bmp expression on Cer1. Cer1 binds at least Bmp2/4 and antagonizes Bmp signalling in cell culture. In line with this, supplementation of Bmp4 restored the ureteric bud tip number, which was reduced by Cer1+ to bring it closer to the normal, consistent with models suggesting that Bmp signalling inhibits ureteric bud development. Genetic reduction of Wnt11 inhibited the Cer1-stimulated kidney development, but Cer1 did not influence Wnt11 signalling in cell culture, although it did inhibit the Wnt3a-induced canonical Top Flash reporter to some extent. We conclude that Cer1 fine tunes the spatial organization of the ureteric tree by coordinating the activities of the growth-promoting ureteric bud signals Gndf and Wnt11 via Bmp-mediated antagonism and to some degree via the canonical Wnt signalling involved in branching. Public Library of Science 2011-11-17 /pmc/articles/PMC3219680/ /pubmed/22114682 http://dx.doi.org/10.1371/journal.pone.0027676 Text en Chi 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
Chi, Lijun
Saarela, Ulla
Railo, Antti
Prunskaite-Hyyryläinen, Renata
Skovorodkin, Ilya
Anthony, Shelagh
Katsu, Kenjiro
Liu, Yu
Shan, Jingdong
Salgueiro, Ana Marisa
Belo, José António
Davies, Jamie
Yokouchi, Yuji
Vainio, Seppo J.
A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development
title A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development
title_full A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development
title_fullStr A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development
title_full_unstemmed A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development
title_short A Secreted BMP Antagonist, Cer1, Fine Tunes the Spatial Organization of the Ureteric Bud Tree during Mouse Kidney Development
title_sort secreted bmp antagonist, cer1, fine tunes the spatial organization of the ureteric bud tree during mouse kidney development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219680/
https://www.ncbi.nlm.nih.gov/pubmed/22114682
http://dx.doi.org/10.1371/journal.pone.0027676
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