Spatiotemporal dynamics of RhoA activity in migrating cells

Olivier Pertz (), Louis Hodgson, Richard L. Klemke and Klaus M. Hahn ()
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Olivier Pertz: University of North Carolina at Chapel Hill
Louis Hodgson: University of North Carolina at Chapel Hill
Richard L. Klemke: The Scripps Research Institute
Klaus M. Hahn: University of North Carolina at Chapel Hill

Nature, 2006, vol. 440, issue 7087, 1069-1072

Abstract: Abstract Rho family GTPases regulate the actin and adhesion dynamics that control cell migration. Current models postulate that Rac promotes membrane protrusion at the leading edge and that RhoA regulates contractility in the cell body1,2. However, there is evidence that RhoA also regulates membrane protrusion3,4. Here we use a fluorescent biosensor, based on a novel design preserving reversible membrane interactions, to visualize the spatiotemporal dynamics of RhoA activity during cell migration. In randomly migrating cells, RhoA activity is concentrated in a sharp band directly at the edge of protrusions. It is observed sporadically in retracting tails, and is low in the cell body. RhoA activity is also associated with peripheral ruffles and pinocytic vesicles, but not with dorsal ruffles induced by platelet-derived growth factor (PDGF). In contrast to randomly migrating cells, PDGF-induced membrane protrusions have low RhoA activity, potentially because PDGF strongly activates Rac, which has previously been shown to antagonize RhoA activity5,6. Our data therefore show that different extracellular cues induce distinct patterns of RhoA signalling during membrane protrusion.

Date: 2006
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DOI: 10.1038/nature04665

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