PEER-REVIEWED PUBLICATION

2026

Mechanically graded granular scaffolds for osteochondral tissue engineering

Mierswa SC, Wheeler EE, et al.

Biomaterials Advances

UC Davis Health, Lawrence Livermore National Laboratory, University of California – Davis

RESEARCH SUMMARY
This study developed photoannealed polyethylene glycol granular scaffolds with a continuous stiffness gradient to model the mechanical transition of the osteochondral unit without introducing the sharp interfaces typical of biphasic scaffold designs. Using microfluidically generated PEG microgels of three diameters, the authors created macroporous scaffolds whose stiffness increased continuously across an 8 mm region from approximately 2–5 kPa to 50–60 kPa. Human mesenchymal stromal cells cultured in these constructs showed position-dependent responses to the local mechanical environment. Softer regions promoted rounded cell morphology, increased glycosaminoglycan-rich matrix deposition, and elevated chondrogenic-associated responses, while stiffer regions promoted cell elongation, greater cytoskeletal tension, increased alkaline phosphatase activity, mineral deposition, and osteogenic marker expression. Smaller and medium microgels amplified these regional effects relative to large microgels, indicating that scaffold architecture and available interfacial surface area influenced how cells interpreted the gradient. Inhibition of actomyosin contractility with blebbistatin reduced cytoskeletal organization and collapsed gradient-dependent transcriptional patterning, showing that tension-dependent mechanotransduction was required for MSC interpretation of the graded scaffold. Overall, the work establishes a single-material, macroporous gradient scaffold platform for studying mechanically regulated osteochondral tissue formation.

CELLSCALE INSTRUMENT USED

MicroTester

Mechanical properties of individual PEG microgels were characterized using a CellScale MicroTester before scaffold assembly. Microgels were placed on an anvil in a PBS water bath at pH 7.25 and compressed over 30 seconds to 50% of their original diameter using a 2 × 2 mm stainless-steel platen attached to a 0.2032 mm tungsten rod. Force and displacement were recorded for each microgel, and compressive modulus was calculated from the linear region of the compressive modulus versus nominal strain curve using a custom Python workflow. The MicroTester data showed that small, medium, and large microgels had comparable intrinsic compressive moduli of roughly 30–35 kPa, with no statistically significant differences across microgel sizes. These results were critical because they confirmed that later differences in cell behaviour within the assembled scaffolds were not caused by differences in the intrinsic stiffness of the individual microgels themselves, but instead arose from the photoimposed scaffold-scale stiffness gradient and the associated microgel architecture.
AUTHORS

Sabrina C. Mierswa, Erika E. Wheeler, Monica L. Moya, J. Kent Leach.

PUBLICATION DETAILS
JOURNAL

Biomaterials Advances

YEAR

2026

INSTITUTIONS

UC Davis Health, Lawrence Livermore National Laboratory, University of California – Davis

COUNTRIES

United States

INSTRUMENT USED

MicroTester

TESTING METHODS

Compression TestingHydrated and Temperature Controlled TestingMicro-Mechanical Testing

RESEARCH APPLICATIONS

Bone Tissue Engineering & MechanicsCartilage and Meniscus MechanicsScaffold Mechanical Testing

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