Rho GTPase dynamics distinguish between models of cortical excitability.

Abstract

The Rho GTPases pattern the cell cortex in a variety of fundamental cell-morphogenetic processes, including division, wound repair, and locomotion. It has recently become apparent that this patterning arises from the ability of the Rho GTPases to self-organize into static and migrating spots, contractile pulses, and propagating waves in cells from yeasts to mammals.¹ These self-organizing Rho GTPase patterns have been explained by a variety of theoretical models that require multiple interacting positive and negative feedback loops. However, it is often difficult, if not impossible, to discriminate between different models simply because the available experimental data do not simultaneously capture the dynamics of multiple molecular concentrations and biomechanical variables at fine spatial and temporal resolution. Specifically, most studies typically provide either the total Rho GTPase signal or the Rho GTPase activity, as reported by various sensors, but not both. Therefore, it remains largely unknown how membrane accumulation of Rho GTPases (i.e., Rho membrane enrichment) is related to Rho activity. Here, we dissect the dynamics of RhoA by simultaneously imaging both total RhoA and active RhoA in propagating waves of Rho activity and F-actin polymerization.^2,3,4,5 We find that within nascent waves, accumulation of active RhoA precedes that of total RhoA, and we exploit this finding to distinguish between two popular theoretical models previously used to explain propagating cortical Rho waves.