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4D morphogenetic tissue engineering via gradient-crosslinked microporous hydrogel scaffolds.

Haitao Yu1, Guodong Wu1, Jian Zhang1

  • 1Cardiovascular Center, The First Hospital of Jilin University, Changchun, Jilin, 130021, China.

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PubMed
Summary
This summary is machine-generated.

Researchers developed shape-morphing, microporous gradient hydrogels for 4D tissue engineering. These dynamic scaffolds improve nutrient transport and cell function, enabling complex tissue development and bone regeneration.

Keywords:
4D fabricationGradientHydrogelMicroporosityTissue engineering

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Area of Science:

  • Biomaterials Science
  • Tissue Engineering
  • Regenerative Medicine

Background:

  • Shape-morphing hydrogels are promising for 4D tissue engineering, but dense networks hinder nutrient diffusion and tissue remodeling.
  • Existing hydrogels often lack porosity, limiting cell infiltration and extracellular matrix development.

Purpose of the Study:

  • To engineer microporous gradient hydrogels with programmable shape morphing for advanced 4D tissue engineering applications.
  • To overcome mass transport limitations in dynamic scaffolds by introducing controlled porosity.

Main Methods:

  • Fabrication of gradient hydrogels using light-attenuation-mediated photocrosslinking and sacrificial gelatin microspheres (GMSs) for microporosity.
  • Tuning GMS content, photocrosslinking time, and construct geometry to control microporosity, mechanical properties, swelling, and shape deformation.
  • Encapsulation of mesenchymal stem cells (MSCs) and osteogenic differentiation to evaluate tissue formation within the gradient hydrogels.

Main Results:

  • Achieved precise control over hydrogel microporosity, stiffness, swelling, and shape-morphing behavior.
  • Demonstrated high cell viability and maintained construct deformability after cell encapsulation.
  • Engineered complex 3D shapes and enhanced bone-like tissue formation (increased ALP activity and calcium deposition) in MSC-laden gradient hydrogels compared to nonporous controls.

Conclusions:

  • Established a versatile platform for creating tunable, microporous gradient hydrogels with spatiotemporal morphing capabilities.
  • The developed hydrogels offer a novel approach for dynamic, cell-instructive scaffolds in 4D tissue engineering.
  • Microporosity significantly enhances osteogenic differentiation and tissue development in shape-morphing scaffolds.