Vimentin bridges scales to convert polarized cell locomotion into coordinated collective migration

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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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Abstract Collective cell migration is central in development and disease. Vimentin is an intermediate filament protein expressed by epithelial cells at the edge of wounds where collective cell migration is most efficient. yet, its functional role in this context remains underexplored. Here, we show that vimentin, over-expressed in cells undergoing partial epithelial to mesenchymal transition at the edge of epithelial monolayers, has a multiscale impact on the whole monolayer mechano-dynamics. Vimentin knock-down delays wound closure, reduces cell coordination, while increasing traction forces exerted by cells on the substratum. It also disrupts the directionality of leader cells migration, as well as the cohesion and coordinated motion of cells deep in the monolayer. We further show that vimentin promotes the conversion of polarized cell locomotion into coordinate collective migration by polarizing actin, focal adhesions and traction forces, sustaining leader cell’s lamellipodium protrusive activity and directionality, while allowing mechanical coupling of leader with follower cells. Altogether, we show that vimentin is essential for bridging polarized single cell locomotion and coordinated collective migration to allow efficient collective migration. Significant statement Epithelial cells migrate coordinately to repair tissue. Vimentin, transiently enriched at the wound edge plays a key role in guiding this process by converting polarized cell locomotion into coordinate collective migration, enabling leader cells to polarize, form stable protrusions, and maintain directed migration, while allowing mechanical coupling of front cells with followers, necessary for efficient coordinated collective migration. These findings reveal vimentin, a known EMT marker, as a novel positive regulator of efficient wound healing.

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last seen: 2026-05-20T01:45:00.602351+00:00