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Force-control at cellular membranes
Force-regulation at cellular membranes relies on dynamic molecular platforms that integrate intra- and extracellular signals to control cell shape and function. To correctly respond to a continuously changing environment, activity of these platforms needs to be tightly controlled in space and time....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914016/ https://www.ncbi.nlm.nih.gov/pubmed/25715331 http://dx.doi.org/10.1080/19490992.2015.1005524 |
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author | Galic, Milos Begemann, Isabell Viplav, Abhiyan Matis, Maja |
author_facet | Galic, Milos Begemann, Isabell Viplav, Abhiyan Matis, Maja |
author_sort | Galic, Milos |
collection | PubMed |
description | Force-regulation at cellular membranes relies on dynamic molecular platforms that integrate intra- and extracellular signals to control cell shape and function. To correctly respond to a continuously changing environment, activity of these platforms needs to be tightly controlled in space and time. Over the last few years, curvature-dependent mechano-chemical signal translation—a receptor-independent signaling mechanism where physical forces at the plasma membrane trigger nanoscale membrane deformations that are then translated into chemical signal transduction cascades—has emerged as a new signaling principle that cells use to regulate forces at the membrane. However, until recently, technical limitations have precluded studies of this force-induced curvature-dependent signaling at the physiological scale. Here, we comment on recent advancements that allow studying curvature-dependent signaling at membranes, and discuss processes where it may be involved in. Considering its general impact on cell function, a particular focus will be put on the curvature-dependence of feedback loops that control actin-based forces at cellular membranes. |
format | Online Article Text |
id | pubmed-4914016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49140162016-07-06 Force-control at cellular membranes Galic, Milos Begemann, Isabell Viplav, Abhiyan Matis, Maja Bioarchitecture Commentary Force-regulation at cellular membranes relies on dynamic molecular platforms that integrate intra- and extracellular signals to control cell shape and function. To correctly respond to a continuously changing environment, activity of these platforms needs to be tightly controlled in space and time. Over the last few years, curvature-dependent mechano-chemical signal translation—a receptor-independent signaling mechanism where physical forces at the plasma membrane trigger nanoscale membrane deformations that are then translated into chemical signal transduction cascades—has emerged as a new signaling principle that cells use to regulate forces at the membrane. However, until recently, technical limitations have precluded studies of this force-induced curvature-dependent signaling at the physiological scale. Here, we comment on recent advancements that allow studying curvature-dependent signaling at membranes, and discuss processes where it may be involved in. Considering its general impact on cell function, a particular focus will be put on the curvature-dependence of feedback loops that control actin-based forces at cellular membranes. Taylor & Francis 2015-02-25 /pmc/articles/PMC4914016/ /pubmed/25715331 http://dx.doi.org/10.1080/19490992.2015.1005524 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Commentary Galic, Milos Begemann, Isabell Viplav, Abhiyan Matis, Maja Force-control at cellular membranes |
title | Force-control at cellular membranes |
title_full | Force-control at cellular membranes |
title_fullStr | Force-control at cellular membranes |
title_full_unstemmed | Force-control at cellular membranes |
title_short | Force-control at cellular membranes |
title_sort | force-control at cellular membranes |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914016/ https://www.ncbi.nlm.nih.gov/pubmed/25715331 http://dx.doi.org/10.1080/19490992.2015.1005524 |
work_keys_str_mv | AT galicmilos forcecontrolatcellularmembranes AT begemannisabell forcecontrolatcellularmembranes AT viplavabhiyan forcecontrolatcellularmembranes AT matismaja forcecontrolatcellularmembranes |