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Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles

Author

Listed:
  • Suchet Nanda

    (TU Dortmund University
    Max Planck Institute of Molecular Physiology)

  • Abram Calderon

    (TU Dortmund University
    Max Planck Institute of Molecular Physiology)

  • Arya Sachan

    (TU Dortmund University)

  • Thanh-Thuy Duong

    (TU Dortmund University
    Max Planck Institute of Molecular Physiology)

  • Johannes Koch

    (Center of Medical Biotechnology, University of Duisburg-Essen)

  • Xiaoyi Xin

    (Umeå Centre for Microbial Research, Umeå University)

  • Djamschid Solouk-Stahlberg

    (TU Dortmund University
    Max Planck Institute of Molecular Physiology)

  • Yao-Wen Wu

    (Umeå Centre for Microbial Research, Umeå University)

  • Perihan Nalbant

    (Center of Medical Biotechnology, University of Duisburg-Essen)

  • Leif Dehmelt

    (TU Dortmund University)

Abstract

Rho GTPases play a key role in the spatio-temporal coordination of cytoskeletal dynamics during cell migration. Here, we directly investigate crosstalk between the major Rho GTPases Rho, Rac and Cdc42 by combining rapid activity perturbation with activity measurements in mammalian cells. These studies reveal that Rac stimulates Rho activity. Direct measurement of spatio-temporal activity patterns show that Rac activity is tightly and precisely coupled to local cell protrusions, followed by Rho activation during retraction. Furthermore, we find that the Rho-activating Lbc-type GEFs Arhgef11 and Arhgef12 are enriched at transient cell protrusions and retractions and recruited to the plasma membrane by active Rac. In addition, their depletion reduces activity crosstalk, cell protrusion-retraction dynamics and migration distance and increases migration directionality. Thus, our study shows that Arhgef11 and Arhgef12 facilitate exploratory cell migration by coordinating cell protrusion and retraction by coupling the activity of the associated regulators Rac and Rho.

Suggested Citation

  • Suchet Nanda & Abram Calderon & Arya Sachan & Thanh-Thuy Duong & Johannes Koch & Xiaoyi Xin & Djamschid Solouk-Stahlberg & Yao-Wen Wu & Perihan Nalbant & Leif Dehmelt, 2023. "Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43875-y
    DOI: 10.1038/s41467-023-43875-y
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    References listed on IDEAS

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    1. Yi I. Wu & Daniel Frey & Oana I. Lungu & Angelika Jaehrig & Ilme Schlichting & Brian Kuhlman & Klaus M. Hahn, 2009. "A genetically encoded photoactivatable Rac controls the motility of living cells," Nature, Nature, vol. 461(7260), pages 104-108, September.
    2. Daniel A. Fletcher & R. Dyche Mullins, 2010. "Cell mechanics and the cytoskeleton," Nature, Nature, vol. 463(7280), pages 485-492, January.
    3. Matthias Machacek & Louis Hodgson & Christopher Welch & Hunter Elliott & Olivier Pertz & Perihan Nalbant & Amy Abell & Gary L. Johnson & Klaus M. Hahn & Gaudenz Danuser, 2009. "Coordination of Rho GTPase activities during cell protrusion," Nature, Nature, vol. 461(7260), pages 99-103, September.
    4. Olivier Pertz & Louis Hodgson & Richard L. Klemke & Klaus M. Hahn, 2006. "Spatiotemporal dynamics of RhoA activity in migrating cells," Nature, Nature, vol. 440(7087), pages 1069-1072, April.
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