Pulsatile contractions and pattern formation in excitable actomyosin cortex.

The actin cortex is an active adaptive material, embedded with complex regulatory networks that can sense, generate, and transmit mechanical forces. The cortex exhibits a wide range of dynamic behaviours, from generating pulsatory contractions and travelling waves to forming organised structures. De...

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Main Authors: Michael F Staddon, Edwin M Munro, Shiladitya Banerjee
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-03-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1009981
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author Michael F Staddon
Edwin M Munro
Shiladitya Banerjee
author_facet Michael F Staddon
Edwin M Munro
Shiladitya Banerjee
author_sort Michael F Staddon
collection DOAJ
description The actin cortex is an active adaptive material, embedded with complex regulatory networks that can sense, generate, and transmit mechanical forces. The cortex exhibits a wide range of dynamic behaviours, from generating pulsatory contractions and travelling waves to forming organised structures. Despite the progress in characterising the biochemical and mechanical components of the actin cortex, the emergent dynamics of this mechanochemical system is poorly understood. Here we develop a reaction-diffusion model for the RhoA signalling network, the upstream regulator for actomyosin assembly and contractility, coupled to an active actomyosin gel, to investigate how the interplay between chemical signalling and mechanical forces regulates stresses and patterns in the cortex. We demonstrate that mechanochemical feedback in the cortex acts to destabilise homogeneous states and robustly generate pulsatile contractions. By tuning active stress in the system, we show that the cortex can generate propagating contraction pulses, form network structures, or exhibit topological turbulence.
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spelling doaj.art-5a7ce46e56aa41339a09e0ab4f0193152022-12-22T00:37:25ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582022-03-01183e100998110.1371/journal.pcbi.1009981Pulsatile contractions and pattern formation in excitable actomyosin cortex.Michael F StaddonEdwin M MunroShiladitya BanerjeeThe actin cortex is an active adaptive material, embedded with complex regulatory networks that can sense, generate, and transmit mechanical forces. The cortex exhibits a wide range of dynamic behaviours, from generating pulsatory contractions and travelling waves to forming organised structures. Despite the progress in characterising the biochemical and mechanical components of the actin cortex, the emergent dynamics of this mechanochemical system is poorly understood. Here we develop a reaction-diffusion model for the RhoA signalling network, the upstream regulator for actomyosin assembly and contractility, coupled to an active actomyosin gel, to investigate how the interplay between chemical signalling and mechanical forces regulates stresses and patterns in the cortex. We demonstrate that mechanochemical feedback in the cortex acts to destabilise homogeneous states and robustly generate pulsatile contractions. By tuning active stress in the system, we show that the cortex can generate propagating contraction pulses, form network structures, or exhibit topological turbulence.https://doi.org/10.1371/journal.pcbi.1009981
spellingShingle Michael F Staddon
Edwin M Munro
Shiladitya Banerjee
Pulsatile contractions and pattern formation in excitable actomyosin cortex.
PLoS Computational Biology
title Pulsatile contractions and pattern formation in excitable actomyosin cortex.
title_full Pulsatile contractions and pattern formation in excitable actomyosin cortex.
title_fullStr Pulsatile contractions and pattern formation in excitable actomyosin cortex.
title_full_unstemmed Pulsatile contractions and pattern formation in excitable actomyosin cortex.
title_short Pulsatile contractions and pattern formation in excitable actomyosin cortex.
title_sort pulsatile contractions and pattern formation in excitable actomyosin cortex
url https://doi.org/10.1371/journal.pcbi.1009981
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AT edwinmmunro pulsatilecontractionsandpatternformationinexcitableactomyosincortex
AT shiladityabanerjee pulsatilecontractionsandpatternformationinexcitableactomyosincortex