Engineering Granular Hydrogels without Interparticle Cross-Linking to Support Multicellular Organization

Advancing three-dimensional (3D) tissue constructs is central to creating <i>in vitro</i> models and engineered tissues that recapitulate biology. Materials that are permissive to cellular behaviors, including proliferation, morphogenesis of multicellular structures, and motility, will support the emergence of tissue structures. Granular hydrogels in which there is no interparticle cross-linking exhibit dynamic properties that may be permissive to such cellular behaviors. However, designing granular hydrogels that lack interparticle cross-linking but support cellular self-organization remains underexplored relative to granular systems stabilized by interparticle cross-linking. In this study, we developed a polyethylene glycol-based granular hydrogel system, with average particle diameters under 40 μm. This granular hydrogel exhibited bulk stress-relaxing behaviors and compatibility with custom microdevices to sustain cell cultures without degradation. The system was studied in conjunction with cocultures of endothelial cells and fibroblasts, known for their spontaneous network formation. Cross-linking, porosity, and cell-adhesive ligands (such as RGD) were manipulated to control system properties. Toward supporting cellular activity, increased porosity was found to enhance the formation of cellular networks, whereas RGD reduced network formation in the system studied. This research highlights the potential of un-cross-linked granular systems to support morphogenetic processes, like vasculogenesis and tissue maturation, offering insights into material design for 3D cell culture systems.

Authors

Institutions

Publication Details

Journal
ACS Biomaterials Science & Engineering
Published
2024-11-25
DOI
https://doi.org/10.1021/acsbiomaterials.4c01563
Citations
8
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
1.48

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Engineering Granular Hydrogels without Interparticle Cross-Linking to Support Multicellular Organization

Melissa A. Luse, Brant E. Isakson, Christopher B. Highley, Natasha L. Claxton
8 citations
ACS Biomaterials Science & Engineering
3D Printing in Biomedical Research
1.48
article

Engineering Granular Hydrogels without Interparticle Cross-Linking to Support Multicellular Organization

Melissa A. Luse, Brant E. Isakson, Christopher B. Highley, Natasha L. Claxton
article en
8 citations

Abstract

Advancing three-dimensional (3D) tissue constructs is central to creating <i>in vitro</i> models and engineered tissues that recapitulate biology. Materials that are permissive to cellular behaviors, including proliferation, morphogenesis of multicellular structures, and motility, will support the emergence of tissue structures. Granular hydrogels in which there is no interparticle cross-linking exhibit dynamic properties that may be permissive to such cellular behaviors. However, designing granular hydrogels that lack interparticle cross-linking but support cellular self-organization remains underexplored relative to granular systems stabilized by interparticle cross-linking. In this study, we developed a polyethylene glycol-based granular hydrogel system, with average particle diameters under 40 μm. This granular hydrogel exhibited bulk stress-relaxing behaviors and compatibility with custom microdevices to sustain cell cultures without degradation. The system was studied in conjunction with cocultures of endothelial cells and fibroblasts, known for their spontaneous network formation. Cross-linking, porosity, and cell-adhesive ligands (such as RGD) were manipulated to control system properties. Toward supporting cellular activity, increased porosity was found to enhance the formation of cellular networks, whereas RGD reduced network formation in the system studied. This research highlights the potential of un-cross-linked granular systems to support morphogenetic processes, like vasculogenesis and tissue maturation, offering insights into material design for 3D cell culture systems.

ACS Biomaterials Science & EngineeringVol. 10(12)
University of Virginia (US)
National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Openalex Percentile: Top 19%
3D Printing in Biomedical Research
1.48
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.