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α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp
Tissue remodeling and shape changes often rely on force-induced cell rearrangements occurring via cell-cell contact dynamics. Epithelial cell-cell contact shape changes are particularly dependent upon E-cadherin adhesion dynamics which are directly influenced by cell-generated and external forces. W...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461907/ https://www.ncbi.nlm.nih.gov/pubmed/37645773 http://dx.doi.org/10.1101/2023.07.28.550975 |
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author | Bush, Joshua Cabe, Jolene I. Conway, Daniel Maruthamuthu, Venkat |
author_facet | Bush, Joshua Cabe, Jolene I. Conway, Daniel Maruthamuthu, Venkat |
author_sort | Bush, Joshua |
collection | PubMed |
description | Tissue remodeling and shape changes often rely on force-induced cell rearrangements occurring via cell-cell contact dynamics. Epithelial cell-cell contact shape changes are particularly dependent upon E-cadherin adhesion dynamics which are directly influenced by cell-generated and external forces. While both the mobility of E-cadherin adhesions and their adhesion strength have been reported before, it is not clear how these two aspects of E-cadherin adhesion dynamics are related. Here, using magnetic pulling cytometry, we applied an accelerated force ramp on the E-cadherin adhesion between an E-cadherin-coated magnetic microbead and an epithelial cell to ascertain this relationship. Our approach enables the determination of the adhesion strength and force-dependent mobility of individual adhesions, which revealed a direct correlation between these key characteristics. Since α-catenin has previously been reported to play a role in both E-cadherin mobility and adhesion strength when studied independently, we also probed epithelial cells in which α-catenin has been knocked out. We found that, in the absence of α-catenin, E-cadherin adhesions not only had lower adhesion strength, as expected, but were also more mobile. We observed that α-catenin was required for the recovery of strained cell-cell contacts and propose that the adhesion strength and force-dependent mobility of E-cadherin adhesions act in tandem to regulate cell-cell contact homeostasis. Our approach introduces a method which relates the force-dependent adhesion mobility to adhesion strength and highlights the morphological role played by α-catenin in E-cadherin adhesion dynamics. |
format | Online Article Text |
id | pubmed-10461907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104619072023-08-29 α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp Bush, Joshua Cabe, Jolene I. Conway, Daniel Maruthamuthu, Venkat bioRxiv Article Tissue remodeling and shape changes often rely on force-induced cell rearrangements occurring via cell-cell contact dynamics. Epithelial cell-cell contact shape changes are particularly dependent upon E-cadherin adhesion dynamics which are directly influenced by cell-generated and external forces. While both the mobility of E-cadherin adhesions and their adhesion strength have been reported before, it is not clear how these two aspects of E-cadherin adhesion dynamics are related. Here, using magnetic pulling cytometry, we applied an accelerated force ramp on the E-cadherin adhesion between an E-cadherin-coated magnetic microbead and an epithelial cell to ascertain this relationship. Our approach enables the determination of the adhesion strength and force-dependent mobility of individual adhesions, which revealed a direct correlation between these key characteristics. Since α-catenin has previously been reported to play a role in both E-cadherin mobility and adhesion strength when studied independently, we also probed epithelial cells in which α-catenin has been knocked out. We found that, in the absence of α-catenin, E-cadherin adhesions not only had lower adhesion strength, as expected, but were also more mobile. We observed that α-catenin was required for the recovery of strained cell-cell contacts and propose that the adhesion strength and force-dependent mobility of E-cadherin adhesions act in tandem to regulate cell-cell contact homeostasis. Our approach introduces a method which relates the force-dependent adhesion mobility to adhesion strength and highlights the morphological role played by α-catenin in E-cadherin adhesion dynamics. Cold Spring Harbor Laboratory 2023-08-19 /pmc/articles/PMC10461907/ /pubmed/37645773 http://dx.doi.org/10.1101/2023.07.28.550975 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Bush, Joshua Cabe, Jolene I. Conway, Daniel Maruthamuthu, Venkat α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp |
title | α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp |
title_full | α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp |
title_fullStr | α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp |
title_full_unstemmed | α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp |
title_short | α-Catenin Dependent E-cadherin Adhesion Dynamics as Revealed by an Accelerated Force Ramp |
title_sort | α-catenin dependent e-cadherin adhesion dynamics as revealed by an accelerated force ramp |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461907/ https://www.ncbi.nlm.nih.gov/pubmed/37645773 http://dx.doi.org/10.1101/2023.07.28.550975 |
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