Tethering Cells via Enzymatic Oxidative Crosslinking Enables Mechanotransduction in Non-Cell-Adhesive Materials

Tom Kamperman*, Sieger Henke, João F. Crispim, Niels G.A. Willemen, Pieter J. Dijkstra, Wooje Lee, Herman L. Offerhaus, Martin Neubauer, Alexandra M. Smink, Paul de Vos, Bart J. de Haan, Marcel Karperien, Su Ryon Shin, Jeroen Leijten*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Cell–matrix interactions govern cell behavior and tissue function by facilitating transduction of biomechanical cues. Engineered tissues often incorporate these interactions by employing cell-adhesive materials. However, using constitutively active cell-adhesive materials impedes control over cell fate and elicits inflammatory responses upon implantation. Here, an alternative cell–material interaction strategy that provides mechanotransducive properties via discrete inducible on-cell crosslinking (DOCKING) of materials, including those that are inherently non-cell-adhesive, is introduced. Specifically, tyramine-functionalized materials are tethered to tyrosines that are naturally present in extracellular protein domains via enzyme-mediated oxidative crosslinking. Temporal control over the stiffness of on-cell tethered 3D microniches reveals that DOCKING uniquely enables lineage programming of stem cells by targeting adhesome-related mechanotransduction pathways acting independently of cell volume changes and spreading. In short, DOCKING represents a bioinspired and cytocompatible cell-tethering strategy that offers new routes to study and engineer cell–material interactions, thereby advancing applications ranging from drug delivery, to cell-based therapy, and cultured meat.

Original languageEnglish
Article number2102660
JournalAdvanced materials
Volume33
Issue number42
Early online date3 Sep 2021
DOIs
Publication statusPublished - 21 Oct 2021

Keywords

  • adhesomes
  • biomechanics
  • cell volume
  • inflammation
  • lineage commitment
  • single-cell analysis
  • stem cell microniches
  • UT-Hybrid-D

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