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AmotL2 integrates polarity and junctional cues to modulate cell shape

The assembly of individual epithelial or endothelial cells into a tight cellular sheet requires stringent control of cell packing and organization. These processes are dependent on the establishment and further integration of cellular junctions, the cytoskeleton and the formation of apical-basal pol...

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Autores principales: Hultin, Sara, Subramani, Aravindh, Hildebrand, Sebastian, Zheng, Yujuan, Majumdar, Arindam, Holmgren, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548744/
https://www.ncbi.nlm.nih.gov/pubmed/28790366
http://dx.doi.org/10.1038/s41598-017-07968-1
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author Hultin, Sara
Subramani, Aravindh
Hildebrand, Sebastian
Zheng, Yujuan
Majumdar, Arindam
Holmgren, Lars
author_facet Hultin, Sara
Subramani, Aravindh
Hildebrand, Sebastian
Zheng, Yujuan
Majumdar, Arindam
Holmgren, Lars
author_sort Hultin, Sara
collection PubMed
description The assembly of individual epithelial or endothelial cells into a tight cellular sheet requires stringent control of cell packing and organization. These processes are dependent on the establishment and further integration of cellular junctions, the cytoskeleton and the formation of apical-basal polarity. However, little is known how these subcellular events are coordinated. The (Angiomotin) Amot protein family consists of scaffold proteins that interact with junctional cadherins, polarity proteins and the cytoskeleton. In this report, we have studied how these protein complexes integrate to control cellular shapes consistent with organ function. Using gene-inactivating studies in zebrafish and cell culture systems in vitro, we show that Par3 to be essential for localization of AmotL2 to cellular junctions to associate with VE/E-cadherin and subsequently the organization of radial actin filaments. Our data provide mechanistic insight in how critical processes such as aortic lumen expansion as well as epithelial packing into hexagonal shapes are controlled.
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spelling pubmed-55487442017-08-09 AmotL2 integrates polarity and junctional cues to modulate cell shape Hultin, Sara Subramani, Aravindh Hildebrand, Sebastian Zheng, Yujuan Majumdar, Arindam Holmgren, Lars Sci Rep Article The assembly of individual epithelial or endothelial cells into a tight cellular sheet requires stringent control of cell packing and organization. These processes are dependent on the establishment and further integration of cellular junctions, the cytoskeleton and the formation of apical-basal polarity. However, little is known how these subcellular events are coordinated. The (Angiomotin) Amot protein family consists of scaffold proteins that interact with junctional cadherins, polarity proteins and the cytoskeleton. In this report, we have studied how these protein complexes integrate to control cellular shapes consistent with organ function. Using gene-inactivating studies in zebrafish and cell culture systems in vitro, we show that Par3 to be essential for localization of AmotL2 to cellular junctions to associate with VE/E-cadherin and subsequently the organization of radial actin filaments. Our data provide mechanistic insight in how critical processes such as aortic lumen expansion as well as epithelial packing into hexagonal shapes are controlled. Nature Publishing Group UK 2017-08-08 /pmc/articles/PMC5548744/ /pubmed/28790366 http://dx.doi.org/10.1038/s41598-017-07968-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hultin, Sara
Subramani, Aravindh
Hildebrand, Sebastian
Zheng, Yujuan
Majumdar, Arindam
Holmgren, Lars
AmotL2 integrates polarity and junctional cues to modulate cell shape
title AmotL2 integrates polarity and junctional cues to modulate cell shape
title_full AmotL2 integrates polarity and junctional cues to modulate cell shape
title_fullStr AmotL2 integrates polarity and junctional cues to modulate cell shape
title_full_unstemmed AmotL2 integrates polarity and junctional cues to modulate cell shape
title_short AmotL2 integrates polarity and junctional cues to modulate cell shape
title_sort amotl2 integrates polarity and junctional cues to modulate cell shape
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548744/
https://www.ncbi.nlm.nih.gov/pubmed/28790366
http://dx.doi.org/10.1038/s41598-017-07968-1
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