Hydrogels possessing
fine-adjustable and switchable elasticity
emulate the mechanical microenvironments of biological cells, which
are known to change dynamically during development and disease progression.
In this study, a supramolecular hydrogel conjugated with gelatin side
chains was synthesized. By systematically screening the molar fraction
of supramolecular host/guest cross-linkers, Young’s modulus
of the substrate was fine-adjusted to the level for myoblasts, E ≈ 10 kPa. C2C12 myoblasts reproducibly and firmly
adhered to the gelatin-conjugated hydrogel via focal adhesion contacts
consisting of integrin clusters, whereas only a few cells adhered
to the gel without gelatin side chains. The elasticity of the gelatin-conjugated
hydrogel was switchable to desired levels by simply adding and removing
free guest molecules in appropriate concentrations without interfering
with cell viability. Immunofluorescence confocal microscopy images
of fixed cells confirmed the adaptation of focal adhesions and remodeling
of actin cytoskeletons on the gelatin-conjugated hydrogel. Time-lapse
phase-contrast images demonstrated the dynamic response of the cells,
manifested in their morphology, to an abrupt change in the substrate
elasticity. Gelatin-conjugated hydrogels with switchable elasticity
enable the direct and reversible mechanical stimulation of cells in
one step without tedious surface functionalization with adhesion ligands.