Microgels With Electrostatically Controlled Molecular Affinity to Direct Morphogenesis
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
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 language | English |
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Article number | 2409731 |
Journal | Advanced materials |
Publication status | E-pub ahead of print - 24 Oct 2024 |
Peer-reviewed | Yes |
External IDs
ORCID | /0000-0003-0189-3448/work/171063121 |
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Keywords
ASJC Scopus subject areas
Keywords
- artificial signaling centers, beads, heparin, kidney organoids, microgels, morphogen gradients, sulfated glycosaminoglycans, vascular morphogenesis, VEGF