The Galapagos Chip Platform for High-Throughput Screening of Cell Adhesive Chemical Micropatterns.

YAP high-throughput screening machine learning mechanosensing micropatterning silane surface modification thiol-ene click chemistry

Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
03 2022
Historique:
revised: 04 11 2021
received: 17 09 2021
pubmed: 6 1 2022
medline: 5 4 2022
entrez: 5 1 2022
Statut: ppublish

Résumé

In vivo cells reside in a complex extracellular matrix (ECM) that presents spatially distributed biochemical and -physical cues at the nano- to micrometer scales. Chemical micropatterning is successfully used to generate adhesive islands to control where and how cells attach and restore cues of the ECM in vitro. Although chemical micropatterning has become a powerful tool to study cell-material interactions, only a fraction of the possible micropattern designs was covered so far, leaving many other possible designs still unexplored. Here, a high-throughput screening platform called "Galapagos chip" is developed. It contains a library of 2176 distinct subcellular chemical patterns created using mathematical algorithms and a straightforward UV-induced two-step surface modification. This approach enables the immobilization of ligands in geometrically defined regions onto cell culture substrates. To validate the system, binary RGD/polyethylene glycol patterns are prepared on which human mesenchymal stem cells are cultured, and the authors observe how different patterns affect cell and organelle morphology. As proof of concept, the cells are stained for the mechanosensitive YAP protein, and, using a machine-learning algorithm, it is demonstrated that cell shape and YAP nuclear translocation correlate. It is concluded that the Galapagos chip is a versatile platform to screen geometrical aspects of cell-ECM interaction.

Identifiants

pubmed: 34985808
doi: 10.1002/smll.202105704
doi:

Substances chimiques

Adhesives 0
Polyethylene Glycols 3WJQ0SDW1A

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2105704

Informations de copyright

© 2022 The Authors. Small published by Wiley-VCH GmbH.

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Auteurs

Urandelger Tuvshindorj (U)

MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, 6229 ER, The Netherlands.
Department of Biomedical Engineering and Institute, for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, 5600 MB, The Netherlands.

Vanessa Trouillet (V)

Institute for Applied Materials and Karlsruhe Nano Micro Facility, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.

Aliaksei Vasilevich (A)

Department of Biomedical Engineering and Institute, for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, 5600 MB, The Netherlands.

Britta Koch (B)

Advanced Materials and Healthcare Technologies Division, The School of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.

Steven Vermeulen (S)

MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, 6229 ER, The Netherlands.

Aurélie Carlier (A)

MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, 6229 ER, The Netherlands.

Morgan R Alexander (MR)

Advanced Materials and Healthcare Technologies Division, The School of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.

Stefan Giselbrecht (S)

MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, 6229 ER, The Netherlands.

Roman Truckenmüller (R)

MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, 6229 ER, The Netherlands.

Jan de Boer (J)

Department of Biomedical Engineering and Institute, for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, 5600 MB, The Netherlands.

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