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Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting
The shape of cellular membranes is highly regulated by a set of conserved mechanisms that can be manipulated by bacterial pathogens to infect cells. Remodeling of the plasma membrane of endothelial cells by the bacterium Neisseria meningitidis is thought to be essential during the blood phase of men...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202395/ https://www.ncbi.nlm.nih.gov/pubmed/30361638 http://dx.doi.org/10.1038/s41467-018-06948-x |
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author | Charles-Orszag, Arthur Tsai, Feng-Ching Bonazzi, Daria Manriquez, Valeria Sachse, Martin Mallet, Adeline Salles, Audrey Melican, Keira Staneva, Ralitza Bertin, Aurélie Millien, Corinne Goussard, Sylvie Lafaye, Pierre Shorte, Spencer Piel, Matthieu Krijnse-Locker, Jacomine Brochard-Wyart, Françoise Bassereau, Patricia Duménil, Guillaume |
author_facet | Charles-Orszag, Arthur Tsai, Feng-Ching Bonazzi, Daria Manriquez, Valeria Sachse, Martin Mallet, Adeline Salles, Audrey Melican, Keira Staneva, Ralitza Bertin, Aurélie Millien, Corinne Goussard, Sylvie Lafaye, Pierre Shorte, Spencer Piel, Matthieu Krijnse-Locker, Jacomine Brochard-Wyart, Françoise Bassereau, Patricia Duménil, Guillaume |
author_sort | Charles-Orszag, Arthur |
collection | PubMed |
description | The shape of cellular membranes is highly regulated by a set of conserved mechanisms that can be manipulated by bacterial pathogens to infect cells. Remodeling of the plasma membrane of endothelial cells by the bacterium Neisseria meningitidis is thought to be essential during the blood phase of meningococcal infection, but the underlying mechanisms are unclear. Here we show that plasma membrane remodeling occurs independently of F-actin, along meningococcal type IV pili fibers, by a physical mechanism that we term ‘one-dimensional’ membrane wetting. We provide a theoretical model that describes the physical basis of one-dimensional wetting and show that this mechanism occurs in model membranes interacting with nanofibers, and in human cells interacting with extracellular matrix meshworks. We propose one-dimensional wetting as a new general principle driving the interaction of cells with their environment at the nanoscale that is diverted by meningococci during infection. |
format | Online Article Text |
id | pubmed-6202395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62023952018-10-29 Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting Charles-Orszag, Arthur Tsai, Feng-Ching Bonazzi, Daria Manriquez, Valeria Sachse, Martin Mallet, Adeline Salles, Audrey Melican, Keira Staneva, Ralitza Bertin, Aurélie Millien, Corinne Goussard, Sylvie Lafaye, Pierre Shorte, Spencer Piel, Matthieu Krijnse-Locker, Jacomine Brochard-Wyart, Françoise Bassereau, Patricia Duménil, Guillaume Nat Commun Article The shape of cellular membranes is highly regulated by a set of conserved mechanisms that can be manipulated by bacterial pathogens to infect cells. Remodeling of the plasma membrane of endothelial cells by the bacterium Neisseria meningitidis is thought to be essential during the blood phase of meningococcal infection, but the underlying mechanisms are unclear. Here we show that plasma membrane remodeling occurs independently of F-actin, along meningococcal type IV pili fibers, by a physical mechanism that we term ‘one-dimensional’ membrane wetting. We provide a theoretical model that describes the physical basis of one-dimensional wetting and show that this mechanism occurs in model membranes interacting with nanofibers, and in human cells interacting with extracellular matrix meshworks. We propose one-dimensional wetting as a new general principle driving the interaction of cells with their environment at the nanoscale that is diverted by meningococci during infection. Nature Publishing Group UK 2018-10-25 /pmc/articles/PMC6202395/ /pubmed/30361638 http://dx.doi.org/10.1038/s41467-018-06948-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Charles-Orszag, Arthur Tsai, Feng-Ching Bonazzi, Daria Manriquez, Valeria Sachse, Martin Mallet, Adeline Salles, Audrey Melican, Keira Staneva, Ralitza Bertin, Aurélie Millien, Corinne Goussard, Sylvie Lafaye, Pierre Shorte, Spencer Piel, Matthieu Krijnse-Locker, Jacomine Brochard-Wyart, Françoise Bassereau, Patricia Duménil, Guillaume Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
title | Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
title_full | Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
title_fullStr | Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
title_full_unstemmed | Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
title_short | Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
title_sort | adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202395/ https://www.ncbi.nlm.nih.gov/pubmed/30361638 http://dx.doi.org/10.1038/s41467-018-06948-x |
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