Trujillo, Juliana, Biomedical Engineering - School of Engineering and Applied Science, University of Virginia
Advisors
Griffin, Donald, Biomedical Engineering, University of Virginia
Abstract
Effective tissue integration of biomaterial scaffolds requires coordinated cellular infiltration driven by gradients of immobilized and soluble migration cues. This is particularly critical in impaired wound healing, where native tissue architecture and endogenous migratory cues are disrupted or lost. Incorporating bioactive signals into hydrogel scaffolds to direct cell migration is a common strategy to promote biomaterial-tissue integration. However, replicating the heterogeneous spatial presentation of these cues characteristic of native extracellular matrix remains a central challenge in translational scaffold design. Synthetic hydrogel systems are commonly functionalized through covalent immobilization of adhesion motifs or uniform exogenous delivery of soluble growth factors, but these approaches fail to replicate the spatially organized, affinity-based growth factor presentation that governs directed cell migration in native tissue. Incorporation of heparin—a negatively charged glycosaminoglycan that l
Degree
PHD (Doctor of Philosophy)
Keywords
biomaterials; cell migration; heparin
Language
English
Rights
All rights reserved by the author (no additional license for public reuse)
Trujillo, Juliana. Heterogeneous Heparin Presentation in Microporous Annealed Particle Scaffolds Modulates Directed Cell Migration. University of Virginia, Biomedical Engineering - School of Engineering and Applied Science, PHD (Doctor of Philosophy), 2026-04-24, https://doi.org/10.18130/afvp-4h63.
Files
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