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Hauptverfasser: Ho, Richard, Lång, Anna, Lång, Emma, Bøe, Stig Ove, Angheluta, Luiza
Format: Preprint
Veröffentlicht: 2026
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Online-Zugang:https://arxiv.org/abs/2605.23339
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author Ho, Richard
Lång, Anna
Lång, Emma
Bøe, Stig Ove
Angheluta, Luiza
author_facet Ho, Richard
Lång, Anna
Lång, Emma
Bøe, Stig Ove
Angheluta, Luiza
contents Transitions from quiescence to collective migration in epithelia underlie wound healing and cancer invasion, yet their physical origin remains poorly understood. Here we show that quiescent epithelial monolayers store spatially contractile stresses that function as a form of mechanical memory. Upon serum-induced reactivation, these pre-stressed regions nucleate extensile asters that emit propagating polarity domain walls. Along these interfaces, topological defects are created, advected and annihilated, leading to defect coarsening with faster kinetics than by elastic interactions. An active elastic model quantitatively reproduces the observed dynamics and identifies stored stress as the origin of rapid topological reorganization. Our results establish a mechanism in which mechanical memory in quiescent epithelia triggers active stress release, driving collective migration via rapid topological ordering, distinct from conventional unjamming and flocking transitions.
format Preprint
id arxiv_https___arxiv_org_abs_2605_23339
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Memory-driven topological ordering during the transition from dormant to migrating epithelia
Ho, Richard
Lång, Anna
Lång, Emma
Bøe, Stig Ove
Angheluta, Luiza
Soft Condensed Matter
Transitions from quiescence to collective migration in epithelia underlie wound healing and cancer invasion, yet their physical origin remains poorly understood. Here we show that quiescent epithelial monolayers store spatially contractile stresses that function as a form of mechanical memory. Upon serum-induced reactivation, these pre-stressed regions nucleate extensile asters that emit propagating polarity domain walls. Along these interfaces, topological defects are created, advected and annihilated, leading to defect coarsening with faster kinetics than by elastic interactions. An active elastic model quantitatively reproduces the observed dynamics and identifies stored stress as the origin of rapid topological reorganization. Our results establish a mechanism in which mechanical memory in quiescent epithelia triggers active stress release, driving collective migration via rapid topological ordering, distinct from conventional unjamming and flocking transitions.
title Memory-driven topological ordering during the transition from dormant to migrating epithelia
topic Soft Condensed Matter
url https://arxiv.org/abs/2605.23339