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Three-dimensional morphodynamic simulations of macropinocytic cups

Macropinocytosis refers to the non-specific uptake of extracellular fluid, which plays ubiquitous roles in cell growth, immune surveillance, and virus entry. Despite its widespread occurrence, it remains unclear how its initial cup-shaped plasma membrane extensions form without any external solid su...

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Detalles Bibliográficos
Autores principales: Saito, Nen, Sawai, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560551/
https://www.ncbi.nlm.nih.gov/pubmed/34755081
http://dx.doi.org/10.1016/j.isci.2021.103087
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author Saito, Nen
Sawai, Satoshi
author_facet Saito, Nen
Sawai, Satoshi
author_sort Saito, Nen
collection PubMed
description Macropinocytosis refers to the non-specific uptake of extracellular fluid, which plays ubiquitous roles in cell growth, immune surveillance, and virus entry. Despite its widespread occurrence, it remains unclear how its initial cup-shaped plasma membrane extensions form without any external solid support, as opposed to the process of particle uptake during phagocytosis. Here, by developing a computational framework that describes the coupling between the bistable reaction-diffusion processes of active signaling patches and membrane deformation, we demonstrated that the protrusive force localized to the edge of the patches can give rise to a self-enclosing cup structure, without further assumptions of local bending or contraction. Efficient uptake requires a balance among the patch size, magnitude of protrusive force, and cortical tension. Furthermore, our model exhibits cyclic cup formation, coexistence of multiple cups, and cup-splitting, indicating that these complex morphologies self-organize via a common mutually-dependent process of reaction-diffusion and membrane deformation.
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spelling pubmed-85605512021-11-08 Three-dimensional morphodynamic simulations of macropinocytic cups Saito, Nen Sawai, Satoshi iScience Article Macropinocytosis refers to the non-specific uptake of extracellular fluid, which plays ubiquitous roles in cell growth, immune surveillance, and virus entry. Despite its widespread occurrence, it remains unclear how its initial cup-shaped plasma membrane extensions form without any external solid support, as opposed to the process of particle uptake during phagocytosis. Here, by developing a computational framework that describes the coupling between the bistable reaction-diffusion processes of active signaling patches and membrane deformation, we demonstrated that the protrusive force localized to the edge of the patches can give rise to a self-enclosing cup structure, without further assumptions of local bending or contraction. Efficient uptake requires a balance among the patch size, magnitude of protrusive force, and cortical tension. Furthermore, our model exhibits cyclic cup formation, coexistence of multiple cups, and cup-splitting, indicating that these complex morphologies self-organize via a common mutually-dependent process of reaction-diffusion and membrane deformation. Elsevier 2021-10-01 /pmc/articles/PMC8560551/ /pubmed/34755081 http://dx.doi.org/10.1016/j.isci.2021.103087 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Saito, Nen
Sawai, Satoshi
Three-dimensional morphodynamic simulations of macropinocytic cups
title Three-dimensional morphodynamic simulations of macropinocytic cups
title_full Three-dimensional morphodynamic simulations of macropinocytic cups
title_fullStr Three-dimensional morphodynamic simulations of macropinocytic cups
title_full_unstemmed Three-dimensional morphodynamic simulations of macropinocytic cups
title_short Three-dimensional morphodynamic simulations of macropinocytic cups
title_sort three-dimensional morphodynamic simulations of macropinocytic cups
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560551/
https://www.ncbi.nlm.nih.gov/pubmed/34755081
http://dx.doi.org/10.1016/j.isci.2021.103087
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