Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hecht, Inbal, Skoge, Monica L., Charest, Pascale G., Ben-Jacob, Eshel, Firtel, Richard A., Loomis, William F., Levine, Herbert, Rappel, Wouter-Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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
_version_ 1782207377019240448
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
work_keys_str_mv AT hechtinbal activatedmembranepatchesguidechemotacticcellmotility
AT skogemonical activatedmembranepatchesguidechemotacticcellmotility
AT charestpascaleg activatedmembranepatchesguidechemotacticcellmotility
AT benjacobeshel activatedmembranepatchesguidechemotacticcellmotility
AT firtelricharda activatedmembranepatchesguidechemotacticcellmotility
AT loomiswilliamf activatedmembranepatchesguidechemotacticcellmotility
AT levineherbert activatedmembranepatchesguidechemotacticcellmotility
AT rappelwouterjan activatedmembranepatchesguidechemotacticcellmotility