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Integrin Conformational Dynamics and Mechanotransduction
The function of the integrin family of receptors as central mediators of cell-extracellular matrix (ECM) and cell–cell adhesion requires a remarkable convergence of interactions and influences. Integrins must be anchored to the cytoskeleton and bound to extracellular ligands in order to provide firm...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688440/ https://www.ncbi.nlm.nih.gov/pubmed/36429013 http://dx.doi.org/10.3390/cells11223584 |
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author | Kolasangiani, Reza Bidone, Tamara C. Schwartz, Martin A. |
author_facet | Kolasangiani, Reza Bidone, Tamara C. Schwartz, Martin A. |
author_sort | Kolasangiani, Reza |
collection | PubMed |
description | The function of the integrin family of receptors as central mediators of cell-extracellular matrix (ECM) and cell–cell adhesion requires a remarkable convergence of interactions and influences. Integrins must be anchored to the cytoskeleton and bound to extracellular ligands in order to provide firm adhesion, with force transmission across this linkage conferring tissue integrity. Integrin affinity to ligands is highly regulated by cell signaling pathways, altering affinity constants by 1000-fold or more, via a series of long-range conformational transitions. In this review, we first summarize basic, well-known features of integrin conformational states and then focus on new information concerning the impact of mechanical forces on these states and interstate transitions. We also discuss how these effects may impact mechansensitive cell functions and identify unanswered questions for future studies. |
format | Online Article Text |
id | pubmed-9688440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96884402022-11-25 Integrin Conformational Dynamics and Mechanotransduction Kolasangiani, Reza Bidone, Tamara C. Schwartz, Martin A. Cells Review The function of the integrin family of receptors as central mediators of cell-extracellular matrix (ECM) and cell–cell adhesion requires a remarkable convergence of interactions and influences. Integrins must be anchored to the cytoskeleton and bound to extracellular ligands in order to provide firm adhesion, with force transmission across this linkage conferring tissue integrity. Integrin affinity to ligands is highly regulated by cell signaling pathways, altering affinity constants by 1000-fold or more, via a series of long-range conformational transitions. In this review, we first summarize basic, well-known features of integrin conformational states and then focus on new information concerning the impact of mechanical forces on these states and interstate transitions. We also discuss how these effects may impact mechansensitive cell functions and identify unanswered questions for future studies. MDPI 2022-11-12 /pmc/articles/PMC9688440/ /pubmed/36429013 http://dx.doi.org/10.3390/cells11223584 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kolasangiani, Reza Bidone, Tamara C. Schwartz, Martin A. Integrin Conformational Dynamics and Mechanotransduction |
title | Integrin Conformational Dynamics and Mechanotransduction |
title_full | Integrin Conformational Dynamics and Mechanotransduction |
title_fullStr | Integrin Conformational Dynamics and Mechanotransduction |
title_full_unstemmed | Integrin Conformational Dynamics and Mechanotransduction |
title_short | Integrin Conformational Dynamics and Mechanotransduction |
title_sort | integrin conformational dynamics and mechanotransduction |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688440/ https://www.ncbi.nlm.nih.gov/pubmed/36429013 http://dx.doi.org/10.3390/cells11223584 |
work_keys_str_mv | AT kolasangianireza integrinconformationaldynamicsandmechanotransduction AT bidonetamarac integrinconformationaldynamicsandmechanotransduction AT schwartzmartina integrinconformationaldynamicsandmechanotransduction |