Guiding cell adhesion and motility by modulating cross-linking and topographic properties of microgel arrays.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 25 03 2021
accepted: 02 09 2021
entrez: 23 9 2021
pubmed: 24 9 2021
medline: 18 11 2021
Statut: epublish

Résumé

Biomaterial-driven modulation of cell adhesion and migration is a challenging aspect of tissue engineering. Here, we investigated the impact of surface-bound microgel arrays with variable geometry and adjustable cross-linking properties on cell adhesion and migration. We show that cell migration is inversely correlated with microgel array spacing, whereas directionality increases as array spacing increases. Focal adhesion dynamics is also modulated by microgel topography resulting in less dynamic focal adhesions on surface-bound microgels. Microgels also modulate the motility and adhesion of Sertoli cells used as a model for cell migration and adhesion. Both focal adhesion dynamics and speed are reduced on microgels. Interestingly, Gas2L1, a component of the cytoskeleton that mediates the interaction between microtubules and microfilaments, is dispensable for the regulation of cell adhesion and migration on microgels. Finally, increasing microgel cross-linking causes a clear reduction of focal adhesion turnover in Sertoli cells. These findings not only show that spacing and rigidity of surface-grafted microgels arrays can be effectively used to modulate cell adhesion and motility of diverse cellular systems, but they also form the basis for future developments in the fields of medicine and tissue engineering.

Identifiants

pubmed: 34555082
doi: 10.1371/journal.pone.0257495
pii: PONE-D-21-09835
pmc: PMC8460069
doi:

Substances chimiques

Biocompatible Materials 0
Microgels 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0257495

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Janine Riegert (J)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Alexander Töpel (A)

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany.
DWI, Leibniz Institute for Interactive Materials e.V., Aachen, Germany.

Jana Schieren (J)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Renee Coryn (R)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Stella Dibenedetto (S)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Dominik Braunmiller (D)

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany.
DWI, Leibniz Institute for Interactive Materials e.V., Aachen, Germany.

Kamil Zajt (K)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Carmen Schalla (C)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Stephan Rütten (S)

Electron Microscopy Facility, Institute of Pathology, RWTH Aachen University, Aachen, Germany.

Martin Zenke (M)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

Andrij Pich (A)

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany.
DWI, Leibniz Institute for Interactive Materials e.V., Aachen, Germany.

Antonio Sechi (A)

Dept. of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

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Classifications MeSH