Modelling the rheology of living cell cytoplasm: Poroviscoelasticity and fluid-to-solid transition (original) (raw)

Thekkethil, Namshad, Köry, Jakub ORCID logoORCID: https://orcid.org/0000-0002-4476-2547, Guo, Ming, Stewart, Peter S. ORCID logoORCID: https://orcid.org/0000-0002-0971-8057, Hill, Nicholas A. ORCID logoORCID: https://orcid.org/0000-0003-3079-828X and Luo, Xiaoyu ORCID logoORCID: https://orcid.org/0000-0002-8753-4210(2024) Modelling the rheology of living cell cytoplasm: Poroviscoelasticity and fluid-to-solid transition.Biomechanics and Modeling in Mechanobiology, 23, pp. 1551-1569. (doi: 10.1007/s10237-024-01854-2)

Abstract

Eukaryotic cell rheology has important consequences for vital processes such as adhesion, migration, and differentiation. Experiments indicate that cell cytoplasm can exhibit both elastic and viscous characteristics in different regimes, while the transport of fluid (cytosol) through the cross-linked filamentous scaffold (cytoskeleton) is reminiscent of mass transfer by diffusion through a porous medium. To gain insights into this complex rheological behaviour, we construct a computational model for the cell cytoplasm as a poroviscoelastic material formulated on the principles of nonlinear continuum mechanics, where we model the cytoplasm as a porous viscoelastic scaffold with an embedded viscous fluid flowing between the pores to model the cytosol. Baseline simulations (neglecting the viscosity of the cytosol) indicate that the system exhibits seven different regimes across the parameter space spanned by the viscoelastic relaxation timescale of the cytoskeleton and the poroelastic diffusion timescale; these regimes agree qualitatively with experimental measurements. Furthermore, the theoretical model also allows us to elucidate the additional role of pore fluid viscosity, which enters the system as a distinct viscous timescale. We show that increasing this viscous timescale hinders the passage of the pore fluid (reducing the poroelastic diffusion) and makes the cytoplasm rheology increasingly incompressible, shifting the phase boundaries between the regimes.

Item Type: Articles
Additional Information: N.T., J.K., P.S.S, N.A.H., and X.Y.L. acknowledge funding from EPSRC grant no. EP/S030875/1.
Keywords: Cytoplasm, rheology, poroelasticity, viscoelasticity.
Status: Published
Refereed: Yes
Glasgow Author(s) Enlighten ID: Luo, Professor Xiaoyu and Stewart, Professor Peter and Hill, Professor Nicholas and Thekkethil, Mr Namshad and Koery, Dr Jakub
Authors: Thekkethil, N., Köry, J., Guo, M., Stewart, P. S., Hill, N. A., and Luo, X.
College/School: College of Science and Engineering > School of Mathematics and Statistics > Mathematics
Journal Name: Biomechanics and Modeling in Mechanobiology
Publisher: Springer
ISSN: 1617-7959
ISSN (Online): 1617-7940
Published Online: 08 July 2024
Copyright Holders: Copyright © The Author(s) 2024
First Published: First published in Biomechanics and Modeling in Mechanobiology 23:1551-1569
Publisher Policy: Reproduced under a Creative Commons licence

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Funder and Project Information

EPSRC Centre for Multiscale soft tissue mechanics with MIT and POLIMI (SofTMech-MP)

Xiaoyu Luo

EP/S030875/1

M&S - Mathematics

Deposit and Record Details

ID Code: 324669
Depositing User: Mr Matt Mahon
Datestamp: 19 Apr 2024 08:59
Last Modified: 10 Mar 2025 16:42
Date of acceptance: 17 April 2024
Date of first online publication: 8 July 2024
Date Deposited: 19 April 2024
Data Availability Statement: No