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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5548744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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