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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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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