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Proliferation-independent regulation of organ size by Fgf/Notch signaling
Organ morphogenesis depends on the precise orchestration of cell migration, cell shape changes and cell adhesion. We demonstrate that Notch signaling is an integral part of the Wnt and Fgf signaling feedback loop coordinating cell migration and the self-organization of rosette-shaped sensory organs...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5235355/ https://www.ncbi.nlm.nih.gov/pubmed/28085667 http://dx.doi.org/10.7554/eLife.21049 |
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author | Kozlovskaja-Gumbrienė, Agnė Yi, Ren Alexander, Richard Aman, Andy Jiskra, Ryan Nagelberg, Danielle Knaut, Holger McClain, Melainia Piotrowski, Tatjana |
author_facet | Kozlovskaja-Gumbrienė, Agnė Yi, Ren Alexander, Richard Aman, Andy Jiskra, Ryan Nagelberg, Danielle Knaut, Holger McClain, Melainia Piotrowski, Tatjana |
author_sort | Kozlovskaja-Gumbrienė, Agnė |
collection | PubMed |
description | Organ morphogenesis depends on the precise orchestration of cell migration, cell shape changes and cell adhesion. We demonstrate that Notch signaling is an integral part of the Wnt and Fgf signaling feedback loop coordinating cell migration and the self-organization of rosette-shaped sensory organs in the zebrafish lateral line system. We show that Notch signaling acts downstream of Fgf signaling to not only inhibit hair cell differentiation but also to induce and maintain stable epithelial rosettes. Ectopic Notch expression causes a significant increase in organ size independently of proliferation and the Hippo pathway. Transplantation and RNASeq analyses revealed that Notch signaling induces apical junctional complex genes that regulate cell adhesion and apical constriction. Our analysis also demonstrates that in the absence of patterning cues normally provided by a Wnt/Fgf signaling system, rosettes still self-organize in the presence of Notch signaling. DOI: http://dx.doi.org/10.7554/eLife.21049.001 |
format | Online Article Text |
id | pubmed-5235355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52353552017-01-17 Proliferation-independent regulation of organ size by Fgf/Notch signaling Kozlovskaja-Gumbrienė, Agnė Yi, Ren Alexander, Richard Aman, Andy Jiskra, Ryan Nagelberg, Danielle Knaut, Holger McClain, Melainia Piotrowski, Tatjana eLife Cell Biology Organ morphogenesis depends on the precise orchestration of cell migration, cell shape changes and cell adhesion. We demonstrate that Notch signaling is an integral part of the Wnt and Fgf signaling feedback loop coordinating cell migration and the self-organization of rosette-shaped sensory organs in the zebrafish lateral line system. We show that Notch signaling acts downstream of Fgf signaling to not only inhibit hair cell differentiation but also to induce and maintain stable epithelial rosettes. Ectopic Notch expression causes a significant increase in organ size independently of proliferation and the Hippo pathway. Transplantation and RNASeq analyses revealed that Notch signaling induces apical junctional complex genes that regulate cell adhesion and apical constriction. Our analysis also demonstrates that in the absence of patterning cues normally provided by a Wnt/Fgf signaling system, rosettes still self-organize in the presence of Notch signaling. DOI: http://dx.doi.org/10.7554/eLife.21049.001 eLife Sciences Publications, Ltd 2017-01-13 /pmc/articles/PMC5235355/ /pubmed/28085667 http://dx.doi.org/10.7554/eLife.21049 Text en © 2017, Kozlovskaja-Gumbrienė 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 | Cell Biology Kozlovskaja-Gumbrienė, Agnė Yi, Ren Alexander, Richard Aman, Andy Jiskra, Ryan Nagelberg, Danielle Knaut, Holger McClain, Melainia Piotrowski, Tatjana Proliferation-independent regulation of organ size by Fgf/Notch signaling |
title | Proliferation-independent regulation of organ size by Fgf/Notch signaling |
title_full | Proliferation-independent regulation of organ size by Fgf/Notch signaling |
title_fullStr | Proliferation-independent regulation of organ size by Fgf/Notch signaling |
title_full_unstemmed | Proliferation-independent regulation of organ size by Fgf/Notch signaling |
title_short | Proliferation-independent regulation of organ size by Fgf/Notch signaling |
title_sort | proliferation-independent regulation of organ size by fgf/notch signaling |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5235355/ https://www.ncbi.nlm.nih.gov/pubmed/28085667 http://dx.doi.org/10.7554/eLife.21049 |
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