Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters
Abstract The cellular interaction with the extracellular matrix (ECM) modulates many key processes such as proliferation, migration, differentiation and survival. In addition, cells cultured under 3D conditions in presence of an ECM display a marked radioresistance towards ionizing radiation (IR) in...
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Nature Portfolio
2017-06-01
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Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-017-03414-4 |
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author | Laura Babel Miriam Grunewald Robert Lehn Markus Langhans Tobias Meckel |
author_facet | Laura Babel Miriam Grunewald Robert Lehn Markus Langhans Tobias Meckel |
author_sort | Laura Babel |
collection | DOAJ |
description | Abstract The cellular interaction with the extracellular matrix (ECM) modulates many key processes such as proliferation, migration, differentiation and survival. In addition, cells cultured under 3D conditions in presence of an ECM display a marked radioresistance towards ionizing radiation (IR) in comparison to conventionally 2D cultured cells. This process, also known as “cell-adhesion-mediated-radio-resistance” (CAM-RR), has been linked to the chromatin structure that differs between cells cultured on stiff surfaces versus cell grown on soft planar supports or in 3D environments. As integrins are the key mediators of cell adhesion and mechanosensing, they originate the molecular signalling towards chromatin remodelling in response to a cell’s microenvironment. We aimed to investigate this molecular origin that leads to CAM-RR by investigating the distribution of integrins at the single molecule level and show that cells cultured in 2D keep a lower fraction of integrin β1 in clusters and maintain a less defined cluster status than 3D cultured cells. Upon X-irradiation this nanoscale distribution of integrin β1 is disturbed at much lower dosages in 2D versus 3D cultured cells. Radioresistance is thus linked to the ability to maintain a well defined organization of integrins in clusters, making integrin distribution a potential drug target for radiosensitization. |
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language | English |
last_indexed | 2024-12-18T04:42:28Z |
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spelling | doaj.art-2d8d543f15cf44068dd3f9191096d2612022-12-21T21:20:40ZengNature PortfolioScientific Reports2045-23222017-06-017111310.1038/s41598-017-03414-4Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clustersLaura Babel0Miriam Grunewald1Robert Lehn2Markus Langhans3Tobias Meckel4Membrane Dynamics, Department of Biology, Technische Universität DarmstadtMembrane Dynamics, Department of Biology, Technische Universität DarmstadtMembrane Dynamics, Department of Biology, Technische Universität DarmstadtMembrane Dynamics, Department of Biology, Technische Universität DarmstadtMembrane Dynamics, Department of Biology, Technische Universität DarmstadtAbstract The cellular interaction with the extracellular matrix (ECM) modulates many key processes such as proliferation, migration, differentiation and survival. In addition, cells cultured under 3D conditions in presence of an ECM display a marked radioresistance towards ionizing radiation (IR) in comparison to conventionally 2D cultured cells. This process, also known as “cell-adhesion-mediated-radio-resistance” (CAM-RR), has been linked to the chromatin structure that differs between cells cultured on stiff surfaces versus cell grown on soft planar supports or in 3D environments. As integrins are the key mediators of cell adhesion and mechanosensing, they originate the molecular signalling towards chromatin remodelling in response to a cell’s microenvironment. We aimed to investigate this molecular origin that leads to CAM-RR by investigating the distribution of integrins at the single molecule level and show that cells cultured in 2D keep a lower fraction of integrin β1 in clusters and maintain a less defined cluster status than 3D cultured cells. Upon X-irradiation this nanoscale distribution of integrin β1 is disturbed at much lower dosages in 2D versus 3D cultured cells. Radioresistance is thus linked to the ability to maintain a well defined organization of integrins in clusters, making integrin distribution a potential drug target for radiosensitization.https://doi.org/10.1038/s41598-017-03414-4 |
spellingShingle | Laura Babel Miriam Grunewald Robert Lehn Markus Langhans Tobias Meckel Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters Scientific Reports |
title | Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters |
title_full | Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters |
title_fullStr | Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters |
title_full_unstemmed | Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters |
title_short | Direct evidence for cell adhesion-mediated radioresistance (CAM-RR) on the level of individual integrin β1 clusters |
title_sort | direct evidence for cell adhesion mediated radioresistance cam rr on the level of individual integrin β1 clusters |
url | https://doi.org/10.1038/s41598-017-03414-4 |
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