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Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length

In many biological settings, two or more cells come into physical contact to form a cell-cell interface. In some cases, the cell-cell contact must be transient, forming on timescales of seconds. One example is offered by the T cell, an immune cell which must attach to the surface of other cells in o...

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Autores principales: Liu, Kai, Chu, Brian, Newby, Jay, Read, Elizabeth L., Lowengrub, John, Allard, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504115/
https://www.ncbi.nlm.nih.gov/pubmed/31022168
http://dx.doi.org/10.1371/journal.pcbi.1006352
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author Liu, Kai
Chu, Brian
Newby, Jay
Read, Elizabeth L.
Lowengrub, John
Allard, Jun
author_facet Liu, Kai
Chu, Brian
Newby, Jay
Read, Elizabeth L.
Lowengrub, John
Allard, Jun
author_sort Liu, Kai
collection PubMed
description In many biological settings, two or more cells come into physical contact to form a cell-cell interface. In some cases, the cell-cell contact must be transient, forming on timescales of seconds. One example is offered by the T cell, an immune cell which must attach to the surface of other cells in order to decipher information about disease. The aspect ratio of these interfaces (tens of nanometers thick and tens of micrometers in diameter) puts them into the thin-layer limit, or “lubrication limit”, of fluid dynamics. A key question is how the receptors and ligands on opposing cells come into contact. What are the relative roles of thermal undulations of the plasma membrane and deterministic forces from active filopodia? We use a computational fluid dynamics algorithm capable of simulating 10-nanometer-scale fluid-structure interactions with thermal fluctuations up to seconds- and microns-scales. We use this to simulate two opposing membranes, variously including thermal fluctuations, active forces, and membrane permeability. In some regimes dominated by thermal fluctuations, proximity is a rare event, which we capture by computing mean first-passage times using a Weighted Ensemble rare-event computational method. Our results demonstrate a parameter regime in which the time it takes for an active force to drive local contact actually increases if the cells are being held closer together (e.g., by nonspecific adhesion), a phenomenon we attribute to the thin-layer effect. This leads to an optimal initial cell-cell separation for fastest receptor-ligand binding, which could have relevance for the role of cellular protrusions like microvilli. We reproduce a previous experimental observation that fluctuation spatial scales are largely unaffected, but timescales are dramatically slowed, by the thin-layer effect. We also find that membrane permeability would need to be above physiological levels to abrogate the thin-layer effect.
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spelling pubmed-65041152019-05-09 Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length Liu, Kai Chu, Brian Newby, Jay Read, Elizabeth L. Lowengrub, John Allard, Jun PLoS Comput Biol Research Article In many biological settings, two or more cells come into physical contact to form a cell-cell interface. In some cases, the cell-cell contact must be transient, forming on timescales of seconds. One example is offered by the T cell, an immune cell which must attach to the surface of other cells in order to decipher information about disease. The aspect ratio of these interfaces (tens of nanometers thick and tens of micrometers in diameter) puts them into the thin-layer limit, or “lubrication limit”, of fluid dynamics. A key question is how the receptors and ligands on opposing cells come into contact. What are the relative roles of thermal undulations of the plasma membrane and deterministic forces from active filopodia? We use a computational fluid dynamics algorithm capable of simulating 10-nanometer-scale fluid-structure interactions with thermal fluctuations up to seconds- and microns-scales. We use this to simulate two opposing membranes, variously including thermal fluctuations, active forces, and membrane permeability. In some regimes dominated by thermal fluctuations, proximity is a rare event, which we capture by computing mean first-passage times using a Weighted Ensemble rare-event computational method. Our results demonstrate a parameter regime in which the time it takes for an active force to drive local contact actually increases if the cells are being held closer together (e.g., by nonspecific adhesion), a phenomenon we attribute to the thin-layer effect. This leads to an optimal initial cell-cell separation for fastest receptor-ligand binding, which could have relevance for the role of cellular protrusions like microvilli. We reproduce a previous experimental observation that fluctuation spatial scales are largely unaffected, but timescales are dramatically slowed, by the thin-layer effect. We also find that membrane permeability would need to be above physiological levels to abrogate the thin-layer effect. Public Library of Science 2019-04-25 /pmc/articles/PMC6504115/ /pubmed/31022168 http://dx.doi.org/10.1371/journal.pcbi.1006352 Text en © 2019 Liu 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Kai
Chu, Brian
Newby, Jay
Read, Elizabeth L.
Lowengrub, John
Allard, Jun
Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length
title Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length
title_full Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length
title_fullStr Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length
title_full_unstemmed Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length
title_short Hydrodynamics of transient cell-cell contact: The role of membrane permeability and active protrusion length
title_sort hydrodynamics of transient cell-cell contact: the role of membrane permeability and active protrusion length
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504115/
https://www.ncbi.nlm.nih.gov/pubmed/31022168
http://dx.doi.org/10.1371/journal.pcbi.1006352
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