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An apicobasal gradient of Rac activity determines protrusion form and position

Each cell within a polarized epithelial sheet must align and correctly position a wide range of subcellular structures, including actin-based dynamic protrusions. Using in vivo inducible transgenes that can sense or modify Rac activity, we demonstrate an apicobasal gradient of Rac activity that is r...

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Detalles Bibliográficos
Autores principales: Couto, Africa, Mack, Natalie Ann, Favia, Lucrezia, Georgiou, Marios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454455/
https://www.ncbi.nlm.nih.gov/pubmed/28524861
http://dx.doi.org/10.1038/ncomms15385
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author Couto, Africa
Mack, Natalie Ann
Favia, Lucrezia
Georgiou, Marios
author_facet Couto, Africa
Mack, Natalie Ann
Favia, Lucrezia
Georgiou, Marios
author_sort Couto, Africa
collection PubMed
description Each cell within a polarized epithelial sheet must align and correctly position a wide range of subcellular structures, including actin-based dynamic protrusions. Using in vivo inducible transgenes that can sense or modify Rac activity, we demonstrate an apicobasal gradient of Rac activity that is required to correctly form and position distinct classes of dynamic protrusion along the apicobasal axis of the cell. We show that we can modify the Rac activity gradient in genetic mutants for specific polarity proteins, with consequent changes in protrusion form and position and additionally show, using photoactivatable Rac transgenes, that it is the level of Rac activity that determines protrusion form. Thus, we demonstrate a mechanism by which polarity proteins can spatially regulate Rac activity and the actin cytoskeleton to ensure correct epithelial cell shape and prevent epithelial-to-mesenchymal transitions.
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spelling pubmed-54544552017-06-07 An apicobasal gradient of Rac activity determines protrusion form and position Couto, Africa Mack, Natalie Ann Favia, Lucrezia Georgiou, Marios Nat Commun Article Each cell within a polarized epithelial sheet must align and correctly position a wide range of subcellular structures, including actin-based dynamic protrusions. Using in vivo inducible transgenes that can sense or modify Rac activity, we demonstrate an apicobasal gradient of Rac activity that is required to correctly form and position distinct classes of dynamic protrusion along the apicobasal axis of the cell. We show that we can modify the Rac activity gradient in genetic mutants for specific polarity proteins, with consequent changes in protrusion form and position and additionally show, using photoactivatable Rac transgenes, that it is the level of Rac activity that determines protrusion form. Thus, we demonstrate a mechanism by which polarity proteins can spatially regulate Rac activity and the actin cytoskeleton to ensure correct epithelial cell shape and prevent epithelial-to-mesenchymal transitions. Nature Publishing Group 2017-05-19 /pmc/articles/PMC5454455/ /pubmed/28524861 http://dx.doi.org/10.1038/ncomms15385 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Couto, Africa
Mack, Natalie Ann
Favia, Lucrezia
Georgiou, Marios
An apicobasal gradient of Rac activity determines protrusion form and position
title An apicobasal gradient of Rac activity determines protrusion form and position
title_full An apicobasal gradient of Rac activity determines protrusion form and position
title_fullStr An apicobasal gradient of Rac activity determines protrusion form and position
title_full_unstemmed An apicobasal gradient of Rac activity determines protrusion form and position
title_short An apicobasal gradient of Rac activity determines protrusion form and position
title_sort apicobasal gradient of rac activity determines protrusion form and position
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454455/
https://www.ncbi.nlm.nih.gov/pubmed/28524861
http://dx.doi.org/10.1038/ncomms15385
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