Glassy dynamics in active epithelia emerge from an interplay of mechanochemical feedback and crowding

Fuente: arXiv
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Main Authors: Muthukrishnan, Sindhu, Dewan, Phanindra, Tejaswi, Tanishq, Sebastian, Michelle B, Chhabra, Tanya, Mondal, Soumyadeep, Kolya, Soumitra, Sarkar, Sumantra, Vishwakarma, Medhavi
Format: Preprint
Published: 2025
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author Muthukrishnan, Sindhu
Dewan, Phanindra
Tejaswi, Tanishq
Sebastian, Michelle B
Chhabra, Tanya
Mondal, Soumyadeep
Kolya, Soumitra
Sarkar, Sumantra
Vishwakarma, Medhavi
author_facet Muthukrishnan, Sindhu
Dewan, Phanindra
Tejaswi, Tanishq
Sebastian, Michelle B
Chhabra, Tanya
Mondal, Soumyadeep
Kolya, Soumitra
Sarkar, Sumantra
Vishwakarma, Medhavi
contents Glassy dynamics in active biological cells remain a subject of debate, as cellular activity rarely slows enough for true glassy features to emerge. In this study, we address this paradox of glassy dynamics in epithelial cells by integrating experimental observations with an active vertex model. We demonstrate that while crowding is essential, it is not sufficient for glassy dynamics to emerge. A mechanochemical feedback loop (MCFL), mediated by cell shape changes through the contractile actomyosin network, is required to drive glass transition in dense epithelial tissues, as revealed via a crosstalk between actin-based cell clustering and dynamic heterogeneity in experiments. Incorporating MCFL into the vertex model reveals contrasting results from those previously predicted by theories -- we show that the MCFL can counteract cell division-induced fluidisation and enable glassy dynamics to emerge through active cell-to-cell communication. Furthermore, our analysis reveals, for the first time, the existence of novel collective mechanochemical oscillations that arise from the crosstalk of two MCFLs. Together, we demonstrate that an interplay between crowding and active mechanochemical feedback enables the emergence of glass-like traits and collective biochemical oscillations in epithelial tissues with active cell-cell contacts.
format Preprint
id arxiv_https___arxiv_org_abs_2511_05469
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Glassy dynamics in active epithelia emerge from an interplay of mechanochemical feedback and crowding
Muthukrishnan, Sindhu
Dewan, Phanindra
Tejaswi, Tanishq
Sebastian, Michelle B
Chhabra, Tanya
Mondal, Soumyadeep
Kolya, Soumitra
Sarkar, Sumantra
Vishwakarma, Medhavi
Biological Physics
Soft Condensed Matter
Glassy dynamics in active biological cells remain a subject of debate, as cellular activity rarely slows enough for true glassy features to emerge. In this study, we address this paradox of glassy dynamics in epithelial cells by integrating experimental observations with an active vertex model. We demonstrate that while crowding is essential, it is not sufficient for glassy dynamics to emerge. A mechanochemical feedback loop (MCFL), mediated by cell shape changes through the contractile actomyosin network, is required to drive glass transition in dense epithelial tissues, as revealed via a crosstalk between actin-based cell clustering and dynamic heterogeneity in experiments. Incorporating MCFL into the vertex model reveals contrasting results from those previously predicted by theories -- we show that the MCFL can counteract cell division-induced fluidisation and enable glassy dynamics to emerge through active cell-to-cell communication. Furthermore, our analysis reveals, for the first time, the existence of novel collective mechanochemical oscillations that arise from the crosstalk of two MCFLs. Together, we demonstrate that an interplay between crowding and active mechanochemical feedback enables the emergence of glass-like traits and collective biochemical oscillations in epithelial tissues with active cell-cell contacts.
title Glassy dynamics in active epithelia emerge from an interplay of mechanochemical feedback and crowding
topic Biological Physics
Soft Condensed Matter
url https://arxiv.org/abs/2511.05469