Cell mechanosensing is regulated by substrate strain energy rather than stiffness

Proc Natl Acad Sci U S A. 2019 Oct 29;116(44):22004-22013. doi: 10.1073/pnas.1904660116. Epub 2019 Sep 30.

Abstract

The ability of cells to perceive the mechanical identity of extracellular matrix, generally known as mechanosensing, is generally depicted as a consequence of an intricate balance between pulling forces actuated by the actin fibers on the adhesion plaques and the mechanical reaction of the supporting material. However, whether the cell is sensitive to the stiffness or to the energy required to deform the material remains unclear. To address this important issue, here the cytoskeleton mechanics of BALB/3T3 and MC3T3 cells seeded on linearly elastic substrates under different levels of deformation were studied. In particular, the effect of prestrain on cell mechanics was evaluated by seeding cells both on substrates with no prestrain and on substrates with different levels of prestrain. Results indicated that cells recognize the existence of prestrain, exhibiting a stiffer cytoskeleton on stretched material compared to cells seeded on unstretched substrate. Cytoskeleton mechanics of cells seeded on stretched material were, in addition, comparable to those measured after the stretching of the substrate and cells together to the same level of deformation. This observation clearly suggests that cell mechanosensing is not mediated only by the stiffness of the substrate, as widely assumed in the literature, but also by the deformation energy associated with the substrate. Indeed, the clutch model, based on the exclusive dependence of cell mechanics upon substrate stiffness, fails to describe our experimental results. By modifying the clutch model equations to incorporate the dependence on the strain energy, we were able to correctly interpret the experimental evidence.

Keywords: cell mechanosensing; mechanobiology; prestrain; strain energy.

MeSH terms

  • Animals
  • Cell Line
  • Extracellular Matrix / metabolism
  • Extracellular Matrix / physiology
  • Focal Adhesions / metabolism
  • Focal Adhesions / physiology
  • Mechanotransduction, Cellular / physiology*
  • Mice
  • Mice, Inbred BALB C
  • NIH 3T3 Cells