Integrin α5β1 nano-presentation regulates collective keratinocyte migration independent of substrate rigidity.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
23 09 2021
Historique:
received: 28 04 2021
accepted: 13 09 2021
entrez: 23 9 2021
pubmed: 24 9 2021
medline: 21 10 2021
Statut: epublish

Résumé

Nanometer-scale properties of the extracellular matrix influence many biological processes, including cell motility. While much information is available for single-cell migration, to date, no knowledge exists on how the nanoscale presentation of extracellular matrix receptors influences collective cell migration. In wound healing, basal keratinocytes collectively migrate on a fibronectin-rich provisional basement membrane to re-epithelialize the injured skin. Among other receptors, the fibronectin receptor integrin α5β1 plays a pivotal role in this process. Using a highly specific integrin α5β1 peptidomimetic combined with nanopatterned hydrogels, we show that keratinocyte sheets regulate their migration ability at an optimal integrin α5β1 nanospacing. This efficiency relies on the effective propagation of stresses within the cell monolayer independent of substrate stiffness. For the first time, this work highlights the importance of extracellular matrix receptor nanoscale organization required for efficient tissue regeneration.

Identifiants

pubmed: 34554089
doi: 10.7554/eLife.69861
pii: 69861
pmc: PMC8460267
doi:
pii:

Substances chimiques

Fibronectins 0
Hydrogels 0
Integrin alpha5beta1 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2021, Di Russo et al.

Déclaration de conflit d'intérêts

JD, JW, TS, HK, JS none, JY None

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Auteurs

Jacopo Di Russo (J)

Max Planck Institute for Medical Research, Heidelberg, Germany.
Interdisciplinary Centre for Clinical Research, Aachen, Germany.
DWI - Leibniz-Institute for Interactive Materials, Forckenbeckstrasse, Aachen, Germany.
Institute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany.

Jennifer L Young (JL)

Max Planck Institute for Medical Research, Heidelberg, Germany.
Mechanobiology Institute, National University of Singapore, Singapore, Singapore.
Department of Biomedical Engineering, National University of Singapore, Singapore, Singapore.

Julian Wr Wegner (JW)

Max Planck Institute for Medical Research, Heidelberg, Germany.

Timmy Steins (T)

Interdisciplinary Centre for Clinical Research, Aachen, Germany.
Institute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany.

Horst Kessler (H)

Institute for Advance Study, Department of Chemistry, Technical University of Munich, Garching, Germany.

Joachim P Spatz (JP)

Max Planck Institute for Medical Research, Heidelberg, Germany.
Institute for Molecular System Engineering - IMSE - Heidelberg University, Heidelberg, Germany.
Max Planck School Matter to Life, Heidelberg, Germany.

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