An excitable Rho GTPase signaling network generates dynamic subcellular contraction patterns

Author:

Graessl Melanie1,Koch Johannes1,Calderon Abram2,Kamps Dominic12,Banerjee Soumya2,Mazel Tomáš2,Schulze Nina1,Jungkurth Jana Kathrin12,Patwardhan Rutuja1,Solouk Djamschid2,Hampe Nico3,Hoffmann Bernd3ORCID,Dehmelt Leif2,Nalbant Perihan1ORCID

Affiliation:

1. Department of Molecular Cell Biology, Center for Medical Biotechnology, University of Duisburg-Essen, Essen, Germany

2. Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology and Fakultät für Chemie und Chemische Biologie, TU Dortmund University, Dortmund, Germany

3. Institute of Complex Systems, Forschungszentrum Jülich, Jülich, Germany

Abstract

Rho GTPase-based signaling networks control cellular dynamics by coordinating protrusions and retractions in space and time. Here, we reveal a signaling network that generates pulses and propagating waves of cell contractions. These dynamic patterns emerge via self-organization from an activator–inhibitor network, in which the small GTPase Rho amplifies its activity by recruiting its activator, the guanine nucleotide exchange factor GEF-H1. Rho also inhibits itself by local recruitment of actomyosin and the associated RhoGAP Myo9b. This network structure enables spontaneous, self-limiting patterns of subcellular contractility that can explore mechanical cues in the extracellular environment. Indeed, actomyosin pulse frequency in cells is altered by matrix elasticity, showing that coupling of contractility pulses to environmental deformations modulates network dynamics. Thus, our study reveals a mechanism that integrates intracellular biochemical and extracellular mechanical signals into subcellular activity patterns to control cellular contractility dynamics.

Funder

MERCUR

Bundesministerium fA1/4r Bildung und Forschung

Deutsche Forschungsgemeinschaft

Marie Skłodowska-Curie Innovative Training Network InCeM

Publisher

Rockefeller University Press

Subject

Cell Biology

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