High-resolution assessment of multidimensional cellular mechanics using label-free refractive-index traction force microscopy.
Moosung LeeHyuntae JeongChaeyeon LeeMahn Jae LeeBenedict Reve DelmoSeokhwi KimJennifer H ShinYong Keun ParkPublished in: Communications biology (2024)
A critical requirement for studying cell mechanics is three-dimensional assessment of cellular shapes and forces with high spatiotemporal resolution. Traction force microscopy with fluorescence imaging enables the measurement of cellular forces, but it is limited by photobleaching and a slow acquisition speed. Here, we present refractive-index traction force microscopy (RI-TFM), which simultaneously quantifies the volumetric morphology and traction force of cells using a high-speed illumination scheme with 0.5-Hz temporal resolution. Without labelling, our method enables quantitative analyses of dry-mass distributions and shear (in-plane) and normal (out-of-plane) tractions of single cells on the extracellular matrix. When combined with a constrained total variation-based deconvolution algorithm, it provides 0.55-Pa shear and 1.59-Pa normal traction sensitivity for a 1-kPa hydrogel substrate. We demonstrate its utility by assessing the effects of compromised intracellular stress and capturing the rapid dynamics of cellular junction formation in the spatiotemporal changes in non-planar traction components.
Keyphrases
- single molecule
- high speed
- high resolution
- label free
- atomic force microscopy
- extracellular matrix
- induced apoptosis
- fluorescence imaging
- cell cycle arrest
- machine learning
- deep learning
- cell death
- photodynamic therapy
- mass spectrometry
- endoplasmic reticulum stress
- single cell
- pi k akt
- bone marrow
- stress induced
- hyaluronic acid
- heat stress
- cell proliferation