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....
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Veröffentlicht in: | Bioarchitecture 2014, Vol.4 (4-5), p.164-168 |
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creator | Galic, Milos Begemann, Isabell Viplav, Abhiyan Matis, Maja |
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. |
doi_str_mv | 10.1080/19490992.2015.1005524 |
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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.</description><identifier>ISSN: 1949-0992</identifier><identifier>EISSN: 1949-100X</identifier><identifier>DOI: 10.1080/19490992.2015.1005524</identifier><identifier>PMID: 25715331</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>actin ; Cell Membrane - metabolism ; Cell Physiological Phenomena - physiology ; curvature ; Humans ; lipid ; plasma membrane ; signaling</subject><ispartof>Bioarchitecture, 2014, Vol.4 (4-5), p.164-168</ispartof><rights>2015 The Author(s). Published with license by Taylor & Francis Group, LLC 2014</rights><rights>2015 The Author(s). 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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.</description><subject>actin</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Physiological Phenomena - physiology</subject><subject>curvature</subject><subject>Humans</subject><subject>lipid</subject><subject>plasma membrane</subject><subject>signaling</subject><issn>1949-0992</issn><issn>1949-100X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><recordid>eNpVUVtLwzAUDqI4mfsJysAXXzpzadLkRZThVBj4ouBbOE0TrbTNTFtl_96UdaLn5dw-vnP5EDojeEGwxFdEpQorRRcUEx5LmHOaHqCToZ7E9PVwjAfQBM3a9gNH46lkEh-jCeUZ4YyRE3Sx8sHYxPimC76aQzc3tqr6CsK8tnUeoLHtKTpyULV2NvopelndPS8fkvXT_ePydp2UlMkuUTnNMmcpKJDSUZnmkBmcG1JIJlwuleIGg3MOVA6WpUI4jnMHTAARzBRsiq53vJs-r21hbNwJKr0JZQ1hqz2U-n-nKd_1m__SqSIpjhxTdDkSBP_Z27bTddkO98QrfN9qIgQTXKQ4i9Dzv7N-h-w_EwE3O0DZOB9q-PahKnQH28oHF99iylYzgvWgh97roQc99KgH-wHXaHwV</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Galic, Milos</creator><creator>Begemann, Isabell</creator><creator>Viplav, Abhiyan</creator><creator>Matis, Maja</creator><general>Taylor & Francis</general><scope>0YH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2014</creationdate><title>Force-control at cellular membranes</title><author>Galic, Milos ; Begemann, Isabell ; Viplav, Abhiyan ; Matis, Maja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i238t-9b277fe2a9a88f284ba7c0bc1d836fb8995c0afffa9bae3466f50bfa36a163cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>actin</topic><topic>Cell Membrane - metabolism</topic><topic>Cell Physiological Phenomena - physiology</topic><topic>curvature</topic><topic>Humans</topic><topic>lipid</topic><topic>plasma membrane</topic><topic>signaling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Galic, Milos</creatorcontrib><creatorcontrib>Begemann, Isabell</creatorcontrib><creatorcontrib>Viplav, Abhiyan</creatorcontrib><creatorcontrib>Matis, Maja</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Bioarchitecture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Galic, Milos</au><au>Begemann, Isabell</au><au>Viplav, Abhiyan</au><au>Matis, Maja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Force-control at cellular membranes</atitle><jtitle>Bioarchitecture</jtitle><addtitle>Bioarchitecture</addtitle><date>2014</date><risdate>2014</risdate><volume>4</volume><issue>4-5</issue><spage>164</spage><epage>168</epage><pages>164-168</pages><issn>1949-0992</issn><eissn>1949-100X</eissn><abstract>Force-regulation at cellular membranes relies on dynamic molecular platforms that integrate intra- and extracellular signals to control cell shape and function. 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subjects | actin Cell Membrane - metabolism Cell Physiological Phenomena - physiology curvature Humans lipid plasma membrane signaling |
title | Force-control at cellular membranes |
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