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Long-range mutual activation establishes Rho and Rac polarity during cell migration

  • Henry De Belly,
  • Andreu F. Gallén,
  • Evelyn Strickland,
  • Dorothy C. Estrada,
  • David Sanchez Godinez,
  • Eric Neiva,
  • Patrick J. Zager,
  • Tamas L. Nagy,
  • Janis K. Burkhardt,
  • Hervé Turlier,
  • Orion D. Weiner

摘要

In migrating cells, the GTPase Rac organizes a protrusive front, whereas Rho organizes a contractile back. How these GTPases are positioned at opposite poles remains unclear. We leverage optogenetics, mechanical perturbations, and mathematical modelling to reveal a surprising mechanochemical long-range mutual activation between front and back polarity programmes that complements their well-known local mutual inhibition. Rac-based protrusions elevate membrane tension, stimulating an mTORC2-dependent activation of Rho at the opposite side of the cell. Conversely, Rho-mediated contractility induces cortical-flow-based regulation of phosphoinositide signalling that triggers Rac activation distally. We develop a minimal mechanochemical model to explain how long-range facilitation, together with local inhibition, enables robust Rho and Rac partitioning. Our findings demonstrate how the actin cortex and plasma membrane interact as an integrated mechanochemical system for long-range Rac–Rho patterning. This circuit is required for efficient polarity and migration in primary human T cells and is conserved in epithelial cells, highlighting the generality of this mechanism.