Quantifying cellular traction forces in three dimensions

TLDR

Cells engage in mechanical force exchange with their extracellular environment through tension generated by the cytoskeleton. A method combining laser scanning confocal microscopy and digital volume correlation tracks and quantifies cell‑mediated deformation of the extracellular matrix in all three spatial dimensions. Time‑lapse confocal imaging of 3T3 fibroblasts on fibronectin‑modified polyacrylamide gels of varying thickness revealed substantial in‑plane and normal displacements that were independent of gel stiffness, demonstrating that normal forces contribute significantly even during nominally two‑dimensional migration.

Abstract

Cells engage in mechanical force exchange with their extracellular environment through tension generated by the cytoskeleton. A method combining laser scanning confocal microscopy (LSCM) and digital volume correlation (DVC) enables tracking and quantification of cell-mediated deformation of the extracellular matrix in all three spatial dimensions. Time-lapse confocal imaging of migrating 3T3 fibroblasts on fibronectin (FN)-modified polyacrylamide gels of varying thickness reveals significant in-plane (x, y) and normal (z) displacements, and illustrates the extent to which cells, even in nominally two-dimensional (2-D) environments, explore their surroundings in all three dimensions. The magnitudes of the measured displacements are independent of the elastic moduli of the gels. Analysis of the normal displacement profiles suggests that normal forces play important roles even in 2-D cell migration.