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      Integrin α5β1 nano-presentation regulates collective keratinocyte migration independent of substrate rigidity

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          Abstract

          Nanometer-scale properties of the extracellular matrix influence many biological processes, including cell motility. While much information is available for single-cell migration, to date, no knowledge exists on how the nanoscale presentation of extracellular matrix receptors influences collective cell migration. In wound healing, basal keratinocytes collectively migrate on a fibronectin-rich provisional basement membrane to re-epithelialize the injured skin. Among other receptors, the fibronectin receptor integrin α5β1 plays a pivotal role in this process. Using a highly specific integrin α5β1 peptidomimetic combined with nanopatterned hydrogels, we show that keratinocyte sheets regulate their migration ability at an optimal integrin α5β1 nanospacing. This efficiency relies on the effective propagation of stresses within the cell monolayer independent of substrate stiffness. For the first time, this work highlights the importance of extracellular matrix receptor nanoscale organization required for efficient tissue regeneration.

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          Most cited references46

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          A Comprehensive Evaluation of the Activity and Selectivity Profile of Ligands for RGD-binding Integrins

          Integrins, a diverse class of heterodimeric cell surface receptors, are key regulators of cell structure and behaviour, affecting cell morphology, proliferation, survival and differentiation. Consequently, mutations in specific integrins, or their deregulated expression, are associated with a variety of diseases. In the last decades, many integrin-specific ligands have been developed and used for modulation of integrin function in medical as well as biophysical studies. The IC50-values reported for these ligands strongly vary and are measured using different cell-based and cell-free systems. A systematic comparison of these values is of high importance for selecting the optimal ligands for given applications. In this study, we evaluate a wide range of ligands for their binding affinity towards the RGD-binding integrins αvβ3, αvβ5, αvβ6, αvβ8, α5β1, αIIbβ3, using homogenous ELISA-like solid phase binding assay.
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            Stretching single talin rod molecules activates vinculin binding.

            The molecular mechanism by which a mechanical stimulus is translated into a chemical response in biological systems is still unclear. We show that mechanical stretching of single cytoplasmic proteins can activate binding of other molecules. We used magnetic tweezers, total internal reflection fluorescence, and atomic force microscopy to investigate the effect of force on the interaction between talin, a protein that links liganded membrane integrins to the cytoskeleton, and vinculin, a focal adhesion protein that is activated by talin binding, leading to reorganization of the cytoskeleton. Application of physiologically relevant forces caused stretching of single talin rods that exposed cryptic binding sites for vinculin. Thus in the talin-vinculin system, molecular mechanotransduction can occur by protein binding after exposure of buried binding sites in the talin-vinculin system. Such protein stretching may be a more general mechanism for force transduction.
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              Tissue stiffening coordinates morphogenesis by triggering collective cell migration in vivo

              Collective cell migration (CCM) is essential for morphogenesis, tissue remodelling, and cancer invasion1,2. In vivo, groups of cells move in an orchestrated way through tissues. This movement requires forces and involves mechanical as well as molecular interactions between cells and their environment. While the role of molecular signals in CCM is comparatively well understood1,2, how tissue mechanics influence CCM in vivo remains unknown. Here we investigated the importance of mechanical cues in the collective migration of the Xenopus laevis neural crest cells, an embryonic cell population whose migratory behaviour has been likened to cancer invasion3. We found that, during morphogenesis, the head mesoderm underlying the cephalic neural crest stiffens. This stiffening initiated an epithelial-to-mesenchymal transition (EMT) in neural crest cells and triggered their collective migration. To detect changes in their mechanical environment, neural crest use integrin/vinculin/talin-mediated mechanosensing. By performing mechanical and molecular manipulations, we showed that mesoderm stiffening is necessary and sufficient to trigger neural crest migration. Finally, we demonstrated that convergent extension of the mesoderm, which starts during gastrulation, leads to increased mesoderm stiffness by increasing the cell density underneath the neural crest. These results unveil a novel role for mesodermal convergent extension as a mechanical coordinator of morphogenesis, and thus reveal a new link between two apparently unconnected processes, gastrulation and neural crest migration, via changes in tissue mechanics. Overall, we provide the first demonstration that changes in substrate stiffness can trigger CCM by promoting EMT in vivo. More broadly, our results raise the exciting idea that tissue mechanics combines with molecular effectors to coordinate morphogenesis4.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                23 September 2021
                2021
                : 10
                : e69861
                Affiliations
                [1 ] Max Planck Institute for Medical Research Heidelberg Germany
                [2 ] Interdisciplinary Centre for Clinical Research Aachen Germany
                [3 ] DWI – Leibniz-Institute for Interactive Materials, Forckenbeckstrasse Aachen Germany
                [4 ] Institute of Molecular and Cellular Anatomy, RWTH Aachen University Aachen Germany
                [5 ] Mechanobiology Institute, National University of Singapore Singapore Singapore
                [6 ] Department of Biomedical Engineering, National University of Singapore Singapore Singapore
                [7 ] Institute for Advance Study, Department of Chemistry, Technical University of Munich Garching Germany
                [8 ] Institute for Molecular System Engineering – IMSE - Heidelberg University Heidelberg Germany
                [9 ] Max Planck School Matter to Life Heidelberg Germany
                Max Planck Institute of Biochemistry Germany
                Fred Hutchinson Cancer Research Center United States
                Max Planck Institute of Biochemistry Germany
                Max Planck Institute of Biochemistry Germany
                Aix Marseille University, CNRS, IDBM France
                Author information
                https://orcid.org/0000-0001-6731-9612
                Article
                69861
                10.7554/eLife.69861
                8460267
                34554089
                8f2a49d5-e120-4a7e-90a8-4c5e0e3c7f2e
                © 2021, Di Russo et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 28 April 2021
                : 13 September 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100007210, RWTH Aachen University;
                Award ID: Interdisciplinary Centre for Clinical Research
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: EXC-2082/1 - 390761711
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100007672, Mechanobiology Institute, Singapore;
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100012319, Max Planck Institute for Dynamics of Complex Technical Systems Magdeburg;
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Cell Biology
                Physics of Living Systems
                Custom metadata
                The use of nanopatterned hydrogels and specific integrin α5β1 peptidomimetic revealed that keratinocytes require an optimum inter-ligand spacing to best propagate intercellular forces and efficiently coordinate cell sheet migration.

                Life sciences
                wound healing,keratocytes,integrin α5β1,collective cell migration,human
                Life sciences
                wound healing, keratocytes, integrin α5β1, collective cell migration, human

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