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Activated Membrane Patches Guide Chemotactic Cell Motility
Many eukaryotic cells are able to crawl on surfaces and guide their motility based on environmental cues. These cues are interpreted by signaling systems which couple to cell mechanics; indeed membrane protrusions in crawling cells are often accompanied by activated membrane patches, which are local...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127810/ https://www.ncbi.nlm.nih.gov/pubmed/21738453 http://dx.doi.org/10.1371/journal.pcbi.1002044 |
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author | Hecht, Inbal Skoge, Monica L. Charest, Pascale G. Ben-Jacob, Eshel Firtel, Richard A. Loomis, William F. Levine, Herbert Rappel, Wouter-Jan |
author_facet | Hecht, Inbal Skoge, Monica L. Charest, Pascale G. Ben-Jacob, Eshel Firtel, Richard A. Loomis, William F. Levine, Herbert Rappel, Wouter-Jan |
author_sort | Hecht, Inbal |
collection | PubMed |
description | Many eukaryotic cells are able to crawl on surfaces and guide their motility based on environmental cues. These cues are interpreted by signaling systems which couple to cell mechanics; indeed membrane protrusions in crawling cells are often accompanied by activated membrane patches, which are localized areas of increased concentration of one or more signaling components. To determine how these patches are related to cell motion, we examine the spatial localization of RasGTP in chemotaxing Dictyostelium discoideum cells under conditions where the vertical extent of the cell was restricted. Quantitative analyses of the data reveal a high degree of spatial correlation between patches of activated Ras and membrane protrusions. Based on these findings, we formulate a model for amoeboid cell motion that consists of two coupled modules. The first module utilizes a recently developed two-component reaction diffusion model that generates transient and localized areas of elevated concentration of one of the components along the membrane. The activated patches determine the location of membrane protrusions (and overall cell motion) that are computed in the second module, which also takes into account the cortical tension and the availability of protrusion resources. We show that our model is able to produce realistic amoeboid-like motion and that our numerical results are consistent with experimentally observed pseudopod dynamics. Specifically, we show that the commonly observed splitting of pseudopods can result directly from the dynamics of the signaling patches. |
format | Online Article Text |
id | pubmed-3127810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31278102011-07-07 Activated Membrane Patches Guide Chemotactic Cell Motility Hecht, Inbal Skoge, Monica L. Charest, Pascale G. Ben-Jacob, Eshel Firtel, Richard A. Loomis, William F. Levine, Herbert Rappel, Wouter-Jan PLoS Comput Biol Research Article Many eukaryotic cells are able to crawl on surfaces and guide their motility based on environmental cues. These cues are interpreted by signaling systems which couple to cell mechanics; indeed membrane protrusions in crawling cells are often accompanied by activated membrane patches, which are localized areas of increased concentration of one or more signaling components. To determine how these patches are related to cell motion, we examine the spatial localization of RasGTP in chemotaxing Dictyostelium discoideum cells under conditions where the vertical extent of the cell was restricted. Quantitative analyses of the data reveal a high degree of spatial correlation between patches of activated Ras and membrane protrusions. Based on these findings, we formulate a model for amoeboid cell motion that consists of two coupled modules. The first module utilizes a recently developed two-component reaction diffusion model that generates transient and localized areas of elevated concentration of one of the components along the membrane. The activated patches determine the location of membrane protrusions (and overall cell motion) that are computed in the second module, which also takes into account the cortical tension and the availability of protrusion resources. We show that our model is able to produce realistic amoeboid-like motion and that our numerical results are consistent with experimentally observed pseudopod dynamics. Specifically, we show that the commonly observed splitting of pseudopods can result directly from the dynamics of the signaling patches. Public Library of Science 2011-06-30 /pmc/articles/PMC3127810/ /pubmed/21738453 http://dx.doi.org/10.1371/journal.pcbi.1002044 Text en Hecht et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hecht, Inbal Skoge, Monica L. Charest, Pascale G. Ben-Jacob, Eshel Firtel, Richard A. Loomis, William F. Levine, Herbert Rappel, Wouter-Jan Activated Membrane Patches Guide Chemotactic Cell Motility |
title | Activated Membrane Patches Guide Chemotactic Cell Motility |
title_full | Activated Membrane Patches Guide Chemotactic Cell Motility |
title_fullStr | Activated Membrane Patches Guide Chemotactic Cell Motility |
title_full_unstemmed | Activated Membrane Patches Guide Chemotactic Cell Motility |
title_short | Activated Membrane Patches Guide Chemotactic Cell Motility |
title_sort | activated membrane patches guide chemotactic cell motility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127810/ https://www.ncbi.nlm.nih.gov/pubmed/21738453 http://dx.doi.org/10.1371/journal.pcbi.1002044 |
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