Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration

Migrating cells need to coordinate distinct leading and trailing edge dynamics but the underlying mechanisms are unclear. Here, we combine experiments and mathematical modeling to elaborate the minimal autonomous biochemical machinery necessary and sufficient for this dynamic coordination and cell m...

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Main Authors: Alfonso Bolado-Carrancio, Oleksii S Rukhlenko, Elena Nikonova, Mikhail A Tsyganov, Anne Wheeler, Amaya Garcia-Munoz, Walter Kolch, Alex von Kriegsheim, Boris N Kholodenko
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-07-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/58165
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spelling doaj-e234ace27d2849c19bad48f7f823ec302021-05-05T21:20:44ZengeLife Sciences Publications LtdeLife2050-084X2020-07-01910.7554/eLife.58165Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migrationAlfonso Bolado-Carrancio0Oleksii S Rukhlenko1https://orcid.org/0000-0003-1863-4987Elena Nikonova2Mikhail A Tsyganov3Anne Wheeler4Amaya Garcia-Munoz5Walter Kolch6Alex von Kriegsheim7https://orcid.org/0000-0002-4952-8573Boris N Kholodenko8https://orcid.org/0000-0002-9483-4975Edinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United KingdomSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, IrelandSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, IrelandSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland; Institute of Theoretical and Experimental Biophysics, Pushchino, Russian FederationEdinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United KingdomSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, IrelandSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland; Conway Institute of Biomolecular & Biomedical Research, University College Dublin, Belfield, IrelandEdinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom; Systems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, IrelandSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland; Conway Institute of Biomolecular & Biomedical Research, University College Dublin, Belfield, Ireland; Department of Pharmacology, Yale University School of Medicine, New Haven, United StatesMigrating cells need to coordinate distinct leading and trailing edge dynamics but the underlying mechanisms are unclear. Here, we combine experiments and mathematical modeling to elaborate the minimal autonomous biochemical machinery necessary and sufficient for this dynamic coordination and cell movement. RhoA activates Rac1 via DIA and inhibits Rac1 via ROCK, while Rac1 inhibits RhoA through PAK. Our data suggest that in motile, polarized cells, RhoA–ROCK interactions prevail at the rear, whereas RhoA-DIA interactions dominate at the front where Rac1/Rho oscillations drive protrusions and retractions. At the rear, high RhoA and low Rac1 activities are maintained until a wave of oscillatory GTPase activities from the cell front reaches the rear, inducing transient GTPase oscillations and RhoA activity spikes. After the rear retracts, the initial GTPase pattern resumes. Our findings show how periodic, propagating GTPase waves coordinate distinct GTPase patterns at the leading and trailing edge dynamics in moving cells.https://elifesciences.org/articles/58165cell migrationrho gtpasesmathematical modelingoscillations and wavesnonlinear dynamics
collection DOAJ
language English
format Article
sources DOAJ
author Alfonso Bolado-Carrancio
Oleksii S Rukhlenko
Elena Nikonova
Mikhail A Tsyganov
Anne Wheeler
Amaya Garcia-Munoz
Walter Kolch
Alex von Kriegsheim
Boris N Kholodenko
spellingShingle Alfonso Bolado-Carrancio
Oleksii S Rukhlenko
Elena Nikonova
Mikhail A Tsyganov
Anne Wheeler
Amaya Garcia-Munoz
Walter Kolch
Alex von Kriegsheim
Boris N Kholodenko
Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration
eLife
cell migration
rho gtpases
mathematical modeling
oscillations and waves
nonlinear dynamics
author_facet Alfonso Bolado-Carrancio
Oleksii S Rukhlenko
Elena Nikonova
Mikhail A Tsyganov
Anne Wheeler
Amaya Garcia-Munoz
Walter Kolch
Alex von Kriegsheim
Boris N Kholodenko
author_sort Alfonso Bolado-Carrancio
title Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration
title_short Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration
title_full Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration
title_fullStr Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration
title_full_unstemmed Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration
title_sort periodic propagating waves coordinate rhogtpase network dynamics at the leading and trailing edges during cell migration
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-07-01
description Migrating cells need to coordinate distinct leading and trailing edge dynamics but the underlying mechanisms are unclear. Here, we combine experiments and mathematical modeling to elaborate the minimal autonomous biochemical machinery necessary and sufficient for this dynamic coordination and cell movement. RhoA activates Rac1 via DIA and inhibits Rac1 via ROCK, while Rac1 inhibits RhoA through PAK. Our data suggest that in motile, polarized cells, RhoA–ROCK interactions prevail at the rear, whereas RhoA-DIA interactions dominate at the front where Rac1/Rho oscillations drive protrusions and retractions. At the rear, high RhoA and low Rac1 activities are maintained until a wave of oscillatory GTPase activities from the cell front reaches the rear, inducing transient GTPase oscillations and RhoA activity spikes. After the rear retracts, the initial GTPase pattern resumes. Our findings show how periodic, propagating GTPase waves coordinate distinct GTPase patterns at the leading and trailing edge dynamics in moving cells.
topic cell migration
rho gtpases
mathematical modeling
oscillations and waves
nonlinear dynamics
url https://elifesciences.org/articles/58165
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