Deformability determines confined cancer cell migration efficiency with limited effect on directionality
A. van der Net (TU Delft - BN/Gijsje Koenderink Lab)
R. C. Boot (TU Delft - ChemE/Product and Process Engineering)
I. Van Dijk (Student TU Delft)
J. P. Conboy (TU Delft - BN/Gijsje Koenderink Lab)
P. E. Boukany (TU Delft - ChemE/Product and Process Engineering)
G. H. Koenderink (TU Delft - BN/Gijsje Koenderink Lab)
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Abstract
Cancer cells can utilize different invasion strategies to overcome physical arrest during confined migration through tissues with small pores. Cancer cell plasticity allows switches between different migration modes and transitions between single-cell and collective migration. The biophysical parameters that guide these decisions are poorly understood. In this work, we investigated the link between cell deformability and migration efficacy in constrictions of two mesenchymal cancer cell-types with similar invasion strategies: HT1080 fibrosarcoma cells and MV3 melanoma cells. To this end, we designed microfluidic platforms for (1) high-throughput cell deformability measurements and (2) migration through a variety of confining geometries. We measured different deformabilities for HT1080 and MV3 cells and correlated this with their migration efficacy through confinements. However, higher deformability and improved squeezing ability did not impact path selection at junctions of channels of different widths. Our findings show that cell deformability correlates with better squeezing abilities through confinements, but minimally impacts confinement directionality.
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