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Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions
Cadherin-mediated adhesions (also known as adherens junctions) are adhesive complexes that connect neighboring cells in a tissue. While the role of the actin cytoskeleton in withstanding tension at these sites of contact is well documented, little is known about the involvement of microtubules and t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247578/ https://www.ncbi.nlm.nih.gov/pubmed/34222239 http://dx.doi.org/10.3389/fcell.2021.669086 |
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author | Joy-Immediato, Michelle Ramirez, Manuel J. Cerda, Mauricio Toyama, Yusuke Ravasio, Andrea Kanchanawong, Pakorn Bertocchi, Cristina |
author_facet | Joy-Immediato, Michelle Ramirez, Manuel J. Cerda, Mauricio Toyama, Yusuke Ravasio, Andrea Kanchanawong, Pakorn Bertocchi, Cristina |
author_sort | Joy-Immediato, Michelle |
collection | PubMed |
description | Cadherin-mediated adhesions (also known as adherens junctions) are adhesive complexes that connect neighboring cells in a tissue. While the role of the actin cytoskeleton in withstanding tension at these sites of contact is well documented, little is known about the involvement of microtubules and the associated endoplasmic reticulum (ER) network in cadherin mechanotransduction. Therefore, we investigated how the organization of ER extensions in close proximity of cadherin-mediated adhesions can affect such complexes, and vice versa. Here, we show that the extension of the ER to cadherin-mediated adhesions is tension dependent and appears to be cadherin-type specific. Furthermore, the different structural organization of the ER/microtubule network seems to affect the localization of ER-bound PTP1B at cadherin-mediated adhesions. This phosphatase is involved in the modulation of vinculin, a molecular clutch which enables differential engagement of the cadherin-catenin layer with the actomyosin cytoskeleton in response to tension. This suggests a link between structural organization of the ER/microtubule network around cadherin-specific adhesions, to control the mechanotransduction of adherens junctions by modulation of vinculin conformational state. |
format | Online Article Text |
id | pubmed-8247578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82475782021-07-02 Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions Joy-Immediato, Michelle Ramirez, Manuel J. Cerda, Mauricio Toyama, Yusuke Ravasio, Andrea Kanchanawong, Pakorn Bertocchi, Cristina Front Cell Dev Biol Cell and Developmental Biology Cadherin-mediated adhesions (also known as adherens junctions) are adhesive complexes that connect neighboring cells in a tissue. While the role of the actin cytoskeleton in withstanding tension at these sites of contact is well documented, little is known about the involvement of microtubules and the associated endoplasmic reticulum (ER) network in cadherin mechanotransduction. Therefore, we investigated how the organization of ER extensions in close proximity of cadherin-mediated adhesions can affect such complexes, and vice versa. Here, we show that the extension of the ER to cadherin-mediated adhesions is tension dependent and appears to be cadherin-type specific. Furthermore, the different structural organization of the ER/microtubule network seems to affect the localization of ER-bound PTP1B at cadherin-mediated adhesions. This phosphatase is involved in the modulation of vinculin, a molecular clutch which enables differential engagement of the cadherin-catenin layer with the actomyosin cytoskeleton in response to tension. This suggests a link between structural organization of the ER/microtubule network around cadherin-specific adhesions, to control the mechanotransduction of adherens junctions by modulation of vinculin conformational state. Frontiers Media S.A. 2021-06-17 /pmc/articles/PMC8247578/ /pubmed/34222239 http://dx.doi.org/10.3389/fcell.2021.669086 Text en Copyright © 2021 Joy-Immediato, Ramirez, Cerda, Toyama, Ravasio, Kanchanawong and Bertocchi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Joy-Immediato, Michelle Ramirez, Manuel J. Cerda, Mauricio Toyama, Yusuke Ravasio, Andrea Kanchanawong, Pakorn Bertocchi, Cristina Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions |
title | Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions |
title_full | Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions |
title_fullStr | Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions |
title_full_unstemmed | Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions |
title_short | Junctional ER Organization Affects Mechanotransduction at Cadherin-Mediated Adhesions |
title_sort | junctional er organization affects mechanotransduction at cadherin-mediated adhesions |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247578/ https://www.ncbi.nlm.nih.gov/pubmed/34222239 http://dx.doi.org/10.3389/fcell.2021.669086 |
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