Bio‐Metamaterials for Mechano‐Regulation of Mesenchymal Stem Cells

Cell behaviors significantly depend on the elastic properties of the microenvironments, which are distinct from commonly used polymer-based substrates. Artificial elastic materials called metamaterials offer large freedom to adjust their effective elastic properties as experienced by cells, provided (i) the metamaterial unit cell is sufficiently small compared to the biological cell size and (ii) the metamaterial is sufficiently soft to deform by the active cell contraction. Thus, metamaterials targeting bio-applications (bio-metamaterials) appear as a promising path toward the mechanical control of stem cells. Herein, human mesenchymal stem cells (hMSCs) are cultured on three different types of planar periodic elastic metamaterials. To fulfill the above two key requirements, microstructured bio-metamaterials have been designed and manufactured based on a silicon elastomer-like photoresist and two-photon laser printing. In addition to the conventional morphometric and immunocytochemical analysis, the traction force that hMSCs exert on metamaterials are inferred by converting the measured displacement-vector fields into force-vector fields. The differential responses of hMSCs, both on the cellular level and the sub-cellular level, correlate with the calculated effective elastic properties of the bio-metamaterials, suggesting the potential of bio-metamaterials toward mechanical regulation of cell behaviors by the arrangement of unit cells

One-Step Synthesis of Gelatin-Conjugated Supramolecular Hydrogels for Dynamic Regulation of Adhesion Contact and Morphology of Myoblasts

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

Reversible Host–Guest Crosslinks in Supramolecular Hydrogels for On‐Demand Mechanical Stimulation of Human Mesenchymal Stem Cells

Stem cells are regulated not only by biochemical signals but also by biophysical properties of extracellular matrix (ECM). The ECM is constantly monitored and remodeled because the fate of stem cells can be misdirected when the mechanical interaction between cells and ECM is imbalanced. A well-defined ECM model for bone marrow-derived human mesenchymal stem cells (hMSCs) based on supramolecular hydrogels containing reversible host–guest crosslinks is fabricated. The stiffness (Young\u27s modulus E) of the hydrogels can be switched reversibly by altering the concentration of non-cytotoxic, free guest molecules dissolved in the culture medium. Fine-adjustment of substrate stiffness enables the authors to determine the critical stiffness level E* at which hMSCs turn the mechano-sensory machinery on or off. Next, the substrate stiffness across E* is switched and the dynamic adaptation characteristics such as morphology, traction force, and YAP/TAZ signaling of hMSCs are monitored. These data demonstrate the instantaneous switching of traction force, which is followed by YAP/TAZ signaling and morphological adaptation. Periodical switching of the substrate stiffness across E* proves that frequent applications of mechanical stimuli drastically suppress hMSC proliferation. Mechanical stimulation across E* level using dynamic hydrogels is a promising strategy for the on-demand control of hMSC transcription and proliferation