Microgels With Electrostatically Controlled Molecular Affinity to Direct Morphogenesis

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Sebastian Kühn - , Leibniz Institute of Polymer Research Dresden (Author)
  • Valentina Magno - , Leibniz Institute of Polymer Research Dresden (Author)
  • Ralf Zimmermann - , Leibniz Institute of Polymer Research Dresden (Author)
  • Yanuar Dwi Putra Limasale - , Leibniz Institute of Polymer Research Dresden (Author)
  • Passant Atallah - , Leibniz Institute of Polymer Research Dresden (Author)
  • Aukha Stoppa - , Leibniz Institute of Polymer Research Dresden (Author)
  • Max J. Männel - , Leibniz Institute of Polymer Research Dresden (Author)
  • Julian Thiele - , Leibniz Institute of Polymer Research Dresden, Otto von Guericke University Magdeburg (Author)
  • Jens Friedrichs - , Leibniz Institute of Polymer Research Dresden (Author)
  • Uwe Freudenberg - , Leibniz Institute of Polymer Research Dresden, TUD Dresden University of Technology (Author)
  • Carsten Werner - , Center for Regenerative Therapies Dresden, Clusters of Excellence PoL: Physics of Life, Chair of Biofunctional Polymer Materials, Leibniz Institute of Polymer Research Dresden (Author)

Abstract

Concentration gradients of soluble signaling molecules—morphogens—determine the cellular organization in tissue development. Morphogen-releasing microgels have shown potential to recapitulate this principle in engineered tissue constructs, however, with limited control over the molecular cues in space and time. Inspired by the functionality of sulfated glycosaminoglycans (sGAGs) in morphogen signaling in vivo, a library of sGAG-based microgels is developed and designated as µGel Units to Instruct Development (µGUIDEs). Adjustment of the microgel's sGAG sulfation patterns and concentration enabled the programming of electrostatic affinities that control the release of morphogens. Based on computational analyses of molecular transport processes, µGUIDEs provided unprecedented precision in the spatiotemporal modulation of vascular endothelial growth factor (VEGF) gradients in a microgel-in-gel vasculogenesis model and kidney organoid cultures. The versatile approach offers new options for creating morphogen signaling centers to advance the understanding of tissue and organ development.

Details

Original languageEnglish
Article number2409731
JournalAdvanced materials
Publication statusE-pub ahead of print - 24 Oct 2024
Peer-reviewedYes

External IDs

ORCID /0000-0003-0189-3448/work/171063121

Keywords

Keywords

  • artificial signaling centers, beads, heparin, kidney organoids, microgels, morphogen gradients, sulfated glycosaminoglycans, vascular morphogenesis, VEGF