Abstract

We describe a method for quantifying the contractile forces that tumor spheroids collectively exert on highly nonlinear three-dimensional collagen networks. While three-dimensional traction force microscopy for single cells in a nonlinear matrix is computationally complex due to the variable cell shape, here we exploit the spherical symmetry of tumor spheroids to derive a scale-invariant relationship between spheroid contractility and the surrounding matrix deformations. This relationship allows us to directly translate the magnitude of matrix deformations to the total contractility of arbitrarily sized spheroids. We show that our method is accurate up to strains of 50% and remains valid even for irregularly shaped tissue samples when considering only the deformations in the far field. Finally, we demonstrate that collective forces of tumor spheroids reflect the contractility of individual cells for up to 1 hr after seeding, while collective forces on longer timescales are guided by mechanical feedback from the extracellular matrix.

Highlights

  • In the pathological process of tumor invasion, cancer cells leave a primary tumor, either individually or collectively[1]

  • Numerous biophysical assays have been developed to quantify the traction forces of individual cancer cells by measuring the deformations that a cell induces in linear elastic substrates (2D and 3D) with known stiffness[4,5,6]

  • Image acquisition can be done with low resolution (4x-10x objective, NA 0.1) brightfield microscopy in combination with micron-sized fiducial markers embedded in the collagen gel to quantify matrix deformations over time (Fig. 1c)

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Summary

Introduction

In the pathological process of tumor invasion, cancer cells leave a primary tumor, either individually or collectively[1]. Numerous biophysical assays have been developed to quantify the traction forces of individual cancer cells by measuring the deformations that a cell induces in linear elastic substrates (2D and 3D) with known stiffness[4,5,6].

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