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Area of Science:

  • Cellular Mechanobiology
  • Biophysics
  • Materials Science

Background:

  • Cellular responses to physical forces (shape, migration, cytoskeleton) are crucial.
  • Cells sense external fibrous environments, modulating internal forces (inside-out).
  • Previous work showed cells respond to fiber curvature and stiffness.

Purpose of the Study:

  • Develop and apply a nanonet platform to measure C2C11 mouse myoblast forces on fibers.
  • Investigate cell adhesion forces under symmetric/asymmetric external perturbations.
  • Extend the platform to study cell-cell junctions, drug effects, and cancer cell morphology.

Main Methods:

  • Utilized a suspended nanonet force microscopy platform.
  • Measured forces of C2C11 myoblasts attached to fibers of varying diameters (250-800 nm).
  • Applied single and cyclic external perturbations in symmetric and asymmetric modes.

Main Results:

  • Inside-out forces are edge-distributed and dependent on fiber structural stiffness.
  • External perturbations biased cell-fiber failure location but not outside-in adhesion forces.
  • Platform extended to measure forces in cell-cell junctions, drug-treated cells, and transitioning cancer cells.

Conclusions:

  • Cellular contractility is sensitive to the mechanical properties of the extracellular fibrous environment.
  • External mechanical cues direct cell-fiber detachment sites without altering adhesion strength.
  • The nanonet platform offers a versatile tool for probing cellular forces in diverse biological contexts.