Cytokinesis machinery promotes cell dissociation from collectively migrating strands in confinement

Cells tune adherens junction dynamics to regulate epithelial integrity in diverse (patho)physiological processes, including cancer metastasis. We hypothesized that the spatially confining architecture of peritumor stroma promotes metastatic cell dissemination by remodeling cell-cell adhesive interactions. By combining microfluidics with live-cell imaging, FLIM/FRET biosensors, and optogenetic tools, we show that confinement induces leader cell dissociation from cohesive ensembles. Cell dissociation is triggered by myosin IIA (MIIA) dismantling of E-cadherin cell-cell junctions, as recapitulated by a mathematical model. Elevated MIIA contractility is controlled by RhoA/ROCK activation, which requires distinct guanine nucleotide exchange factors (GEFs). Confinement activates RhoA via nucleocytoplasmic shuttling of the cytokinesis-regulatory proteins RacGAP1 and Ect2 and increased microtubule dynamics, which results in the release of active GEF-H1. Thus, confining microenvironments are sufficient to induce cell dissemination from primary tumors by remodeling E-cadherin cell junctions via the interplay of microtubules, nuclear trafficking, and RhoA/ROCK/MIIA pathway and not by down-regulating E-cadherin expression.

Automated summary

Cells regulate epithelial integrity and cancer metastasis through adherens junction dynamics. This study shows that the spatial confinement of peritumor stroma promotes metastatic cell dissemination by disrupting cell-cell adhesion. The mechanism involves myosin IIA dismantling E-cadherin junctions, which is controlled by RhoA/ROCK activation mediated by nucleocytoplasmic shuttling of RacGAP1 and Ect2 and increased microtubule dynamics.