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Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions
The formation of healthy tissue involves continuous remodeling of the extracellular matrix (ECM). Whilst it is known that this requires integrin-associated cell-ECM adhesion sites (CMAs) and actomyosin-mediated forces, the underlying mechanisms remain unclear. Here, we examine how tensin3 contribute...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462884/ https://www.ncbi.nlm.nih.gov/pubmed/36074065 http://dx.doi.org/10.1083/jcb.202107022 |
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author | Atherton, Paul Konstantinou, Rafaella Neo, Suat Peng Wang, Emily Balloi, Eleonora Ptushkina, Marina Bennett, Hayley Clark, Kath Gunaratne, Jayantha Critchley, David Barsukov, Igor Manser, Edward Ballestrem, Christoph |
author_facet | Atherton, Paul Konstantinou, Rafaella Neo, Suat Peng Wang, Emily Balloi, Eleonora Ptushkina, Marina Bennett, Hayley Clark, Kath Gunaratne, Jayantha Critchley, David Barsukov, Igor Manser, Edward Ballestrem, Christoph |
author_sort | Atherton, Paul |
collection | PubMed |
description | The formation of healthy tissue involves continuous remodeling of the extracellular matrix (ECM). Whilst it is known that this requires integrin-associated cell-ECM adhesion sites (CMAs) and actomyosin-mediated forces, the underlying mechanisms remain unclear. Here, we examine how tensin3 contributes to the formation of fibrillar adhesions (FBs) and fibronectin fibrillogenesis. Using BioID mass spectrometry and a mitochondrial targeting assay, we establish that tensin3 associates with the mechanosensors such as talin and vinculin. We show that the talin R11 rod domain binds directly to a helical motif within the central intrinsically disordered region (IDR) of tensin3, whilst vinculin binds indirectly to tensin3 via talin. Using CRISPR knock-out cells in combination with defined tensin3 mutations, we show (i) that tensin3 is critical for the formation of α5β1-integrin FBs and for fibronectin fibrillogenesis, and (ii) the talin/tensin3 interaction drives this process, with vinculin acting to potentiate it. |
format | Online Article Text |
id | pubmed-9462884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94628842022-09-27 Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions Atherton, Paul Konstantinou, Rafaella Neo, Suat Peng Wang, Emily Balloi, Eleonora Ptushkina, Marina Bennett, Hayley Clark, Kath Gunaratne, Jayantha Critchley, David Barsukov, Igor Manser, Edward Ballestrem, Christoph J Cell Biol Article The formation of healthy tissue involves continuous remodeling of the extracellular matrix (ECM). Whilst it is known that this requires integrin-associated cell-ECM adhesion sites (CMAs) and actomyosin-mediated forces, the underlying mechanisms remain unclear. Here, we examine how tensin3 contributes to the formation of fibrillar adhesions (FBs) and fibronectin fibrillogenesis. Using BioID mass spectrometry and a mitochondrial targeting assay, we establish that tensin3 associates with the mechanosensors such as talin and vinculin. We show that the talin R11 rod domain binds directly to a helical motif within the central intrinsically disordered region (IDR) of tensin3, whilst vinculin binds indirectly to tensin3 via talin. Using CRISPR knock-out cells in combination with defined tensin3 mutations, we show (i) that tensin3 is critical for the formation of α5β1-integrin FBs and for fibronectin fibrillogenesis, and (ii) the talin/tensin3 interaction drives this process, with vinculin acting to potentiate it. Rockefeller University Press 2022-09-08 /pmc/articles/PMC9462884/ /pubmed/36074065 http://dx.doi.org/10.1083/jcb.202107022 Text en © 2022 Atherton et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Atherton, Paul Konstantinou, Rafaella Neo, Suat Peng Wang, Emily Balloi, Eleonora Ptushkina, Marina Bennett, Hayley Clark, Kath Gunaratne, Jayantha Critchley, David Barsukov, Igor Manser, Edward Ballestrem, Christoph Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
title | Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
title_full | Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
title_fullStr | Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
title_full_unstemmed | Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
title_short | Tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
title_sort | tensin3 interaction with talin drives the formation of fibronectin-associated fibrillar adhesions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462884/ https://www.ncbi.nlm.nih.gov/pubmed/36074065 http://dx.doi.org/10.1083/jcb.202107022 |
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