Long-term imaging of cellular forces with high precision by elastic resonator interference stress microscopy

Nat Cell Biol. 2017 Jul;19(7):864-872. doi: 10.1038/ncb3561. Epub 2017 Jun 19.

Abstract

Cellular forces are crucial for many biological processes but current methods to image them have limitations with respect to data analysis, resolution and throughput. Here, we present a robust approach to measure mechanical cell-substrate interactions in diverse biological systems by interferometrically detecting deformations of an elastic micro-cavity. Elastic resonator interference stress microscopy (ERISM) yields stress maps with exceptional precision and large dynamic range (2 nm displacement resolution over a >1 μm range, translating into 1 pN force sensitivity). This enables investigation of minute vertical stresses (<1 Pa) involved in podosome protrusion, protein-specific cell-substrate interaction and amoeboid migration through spatial confinement in real time. ERISM requires no zero-force reference and avoids phototoxic effects, which facilitates force monitoring over multiple days and at high frame rates and eliminates the need to detach cells after measurements. This allows observation of slow processes such as differentiation and further investigation of cells, for example, by immunostaining.

Publication types

  • Video-Audio Media

MeSH terms

  • 3T3 Cells
  • Animals
  • Biomechanical Phenomena
  • Cell Adhesion
  • Cell Movement*
  • Dictyostelium / metabolism
  • Dictyostelium / physiology*
  • Elasticity
  • Extracellular Matrix / metabolism
  • Fibroblasts / metabolism
  • Fibroblasts / physiology*
  • Humans
  • Macrophages / metabolism
  • Macrophages / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Transgenic
  • Microscopy, Interference / methods*
  • Microscopy, Video
  • Podosomes / metabolism
  • Podosomes / physiology*
  • Stress, Mechanical
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / physiology*
  • Time Factors
  • Time-Lapse Imaging