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Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting

Author

Listed:
  • Arthur Charles-Orszag

    (INSERM, Institut Pasteur
    Université Paris Descartes, Sorbonne Paris Cité)

  • Feng-Ching Tsai

    (Institut Curie, PSL Research University, CNRS UMR168
    Sorbonne Université)

  • Daria Bonazzi

    (INSERM, Institut Pasteur)

  • Valeria Manriquez

    (INSERM, Institut Pasteur
    Université Paris Descartes, Sorbonne Paris Cité)

  • Martin Sachse

    (Ultrapole, Institut Pasteur)

  • Adeline Mallet

    (Ultrapole, Institut Pasteur)

  • Audrey Salles

    (Imagopole, Institut Pasteur)

  • Keira Melican

    (INSERM, Institut Pasteur
    Karolinska Institutet)

  • Ralitza Staneva

    (Institut Curie, PSL Research University, CNRS, UMR 144)

  • Aurélie Bertin

    (Institut Curie, PSL Research University, CNRS UMR168
    Sorbonne Université)

  • Corinne Millien

    (Paris Cardiovascular Research Center)

  • Sylvie Goussard

    (INSERM, Institut Pasteur)

  • Pierre Lafaye

    (Antibody Engineering, Institut Pasteur)

  • Spencer Shorte

    (Imagopole, Institut Pasteur)

  • Matthieu Piel

    (Institut Pierre-Gilles De Gennes
    Institut Curie)

  • Jacomine Krijnse-Locker

    (Ultrapole, Institut Pasteur)

  • Françoise Brochard-Wyart

    (Institut Curie, PSL Research University, CNRS UMR168
    Sorbonne Université)

  • Patricia Bassereau

    (Institut Curie, PSL Research University, CNRS UMR168
    Sorbonne Université)

  • Guillaume Duménil

    (INSERM, Institut Pasteur)

Abstract

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.

Suggested Citation

  • Arthur Charles-Orszag & Feng-Ching Tsai & Daria Bonazzi & Valeria Manriquez & Martin Sachse & Adeline Mallet & Audrey Salles & Keira Melican & Ralitza Staneva & Aurélie Bertin & Corinne Millien & Sylv, 2018. "Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06948-x
    DOI: 10.1038/s41467-018-06948-x
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