Elasticity-dependent response of malignant cells to viscous dissipation.
Elisabeth E CharrierKatarzyna PogodaRobin LiRebecca G WellsPaul A JanmeyPublished in: Biomechanics and modeling in mechanobiology (2020)
The stiffness of the cellular environment controls malignant cell phenotype and proliferation. However, the effect of viscous dissipation on these parameters has not yet been investigated, in part due to the lack of in vitro cell substrates reproducing the mechanical properties of normal tissues and tumors. In this article, we use a newly reported viscoelastic polyacrylamide gel cell substrate, and we characterize the impact of viscous dissipation on three malignant cell lines: DU145 and PC3 derived from prostate and LN229 from brain. The spreading, motility and proliferation rates of these cells were analyzed on 1 kPa and 5 kPa elastic and viscoelastic gels. Surprisingly, the effect of substrate viscous dissipation on cell behavior depended on substrate stiffness for the three cell types tested. We conclude that viscoelasticity controls the spreading, proliferation and migration of malignant cells in vitro. These results highlight the critical role of viscous dissipation in the phenotype and proliferation of malignant cells, especially in stiff tumor environments.
Keyphrases
- induced apoptosis
- single cell
- cell cycle arrest
- cell therapy
- signaling pathway
- prostate cancer
- gene expression
- stem cells
- oxidative stress
- escherichia coli
- high resolution
- cell death
- multiple sclerosis
- mesenchymal stem cells
- cystic fibrosis
- pseudomonas aeruginosa
- pi k akt
- mass spectrometry
- functional connectivity
- resting state
- biofilm formation
- structural basis