14th Annual Symposium
Physics of Cancer
Leipzig, Germany
Oct. 4 - 6, 2023
Contributed Talk
Frictiotaxis underlies adhesion-independent durotaxis
Adam Shellard1, Peter Hampshire2,3, Namid Stillman1, Christina Dix4, Richard Thorogate1, Albane Imbert4, Guillaume Charras1, Ricard Alert2,3, Roberto Mayor1
1University College London, London, UK
2Max Planck Institute for the Physics of Complex Systems, Dresden, Germany
3Center for Systems Biology Dresden, Dresden, Germany
4The Francis Crick Institute, London, UK
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Cells migrate along gradients of substrate stiffness — a process called durotaxis. The physical explanation for durotaxis relies on focal adhesions transmitting the cell’s contractile forces to the substrate. Combining experiments and theory, I will show that confined cells can perform durotaxis despite lacking strong or specific adhesions. We show that the mechanism of this adhesion-independent durotaxis is based on the fact that stiffer substrate offers higher friction. We develop a physical model that predicts that non-adherent cells polarize and migrate towards higher friction — a process that we call frictiotaxis. We demonstrate frictiotaxis in experiments by showing that cells migrate up a friction gradient even when stiffness is uniform. These results broaden the potential of durotaxis to guide any cell that contacts a substrate. Our work also reveals a new mode of directed migration based on friction, with implications for immune and cancer cells, which commonly move with non-specific interactions.
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