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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
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.
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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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