Vimentin bridges scales to convert polarized cell locomotion into coordinated collective migration
The paper studied how the intermediate filament protein vimentin affects collective cell migration during wound closure in epithelial monolayers, using overexpression or knock-down of vimentin in cells undergoing partial epithelial-to-mesenchymal transition at the wound edge. Vimentin knock-down delayed wound closure, reduced cell coordination, disrupted leader-cell directionality, and decreased cohesion and coordinated motion in the monolayer, while also increasing traction forces on the substrate; conversely, vimentin promoted conversion of polarized single-cell locomotion into coordinated collective migration by polarizing actin, focal adhesions, and traction forces and sustaining leader lamellipodium protrusion and directionality. The authors’ main limitation, as implied by the experimental framing, is that findings are based on in vitro monolayer wound models and manipulation of vimentin rather than direct in vivo validation. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.
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- last seen: 2026-05-20T01:45:00.602351+00:00