Matrix stiffness reverses the effect of actomyosin tension on cell proliferation

J Cell Sci. 2012 Dec 15;125(Pt 24):5974-83. doi: 10.1242/jcs.108886. Epub 2012 Oct 24.

Abstract

The stiffness of the extracellular matrix exerts powerful effects on cell proliferation and differentiation, but the mechanisms transducing matrix stiffness into cellular fate decisions remain poorly understood. Two widely reported responses to matrix stiffening are increases in actomyosin contractility and cell proliferation. To delineate their relationship, we modulated cytoskeletal tension in cells grown across a physiological range of matrix stiffnesses. On both synthetic and naturally derived soft matrices, and across a panel of cell types, we observed a striking reversal of the effect of inhibiting actomyosin contractility, switching from the attenuation of proliferation on rigid substrates to the robust promotion of proliferation on soft matrices. Inhibiting contractility on soft matrices decoupled proliferation from cytoskeletal tension and focal adhesion organization, but not from cell spread area. Our results demonstrate that matrix stiffness and actomyosin contractility converge on cell spreading in an unexpected fashion to control a key aspect of cell fate.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Actomyosin / physiology*
  • Amides / pharmacology
  • Animals
  • Cantharidin / pharmacology
  • Cell Adhesion / drug effects
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Dogs
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Extracellular Matrix / physiology*
  • Fibroblasts / cytology*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Heterocyclic Compounds, 4 or More Rings / pharmacology
  • Humans
  • Madin Darby Canine Kidney Cells
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • NIH 3T3 Cells
  • Pyridines / pharmacology
  • Rats

Substances

  • Amides
  • Heterocyclic Compounds, 4 or More Rings
  • Pyridines
  • Y 27632
  • blebbistatin
  • Actomyosin
  • Cantharidin