Wave-pinning and cell polarity from a bistable reaction-diffusion system

Yoichiro Mori, Alexandra Jilkine, Leah Edelstein-Keshet

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295 Scopus citations


Motile eukaryotic cells polarize in response to external signals. Numerous mechanisms have been suggested to account for this symmetry breaking and for the ensuing robust polarization. Implicated in this process are various proteins that are recruited to the plasma membrane and segregate at an emergent front or back of the polarizing cell. Among these are PI3K, PTEN, and members of the Rho family GTPases such as Cdc42, Rac, and Rho. Many such proteins, including the Rho GTPases, cycle between active membrane-bound forms and inactive cytosolic forms. In previous work, we have shown that this property, together with appropriate crosstalk, endows a biochemical circuit (Cdc42, Rac, and Rho) with the property of inherent polarizability. Here we show that this property is present in an even simpler system comprised of a single active/inactive protein pair with positive feedback to its own activation. The simplicity of this minimal system also allows us to explain the mechanism using insights from mathematical analysis. The basic idea resides in a well-known property of reaction-diffusion systems with bistable kinetics, namely, propagation of fronts. However, it crucially depends on exchange between active and inactive forms of the chemicals with unequal rates of diffusion, and overall conservation to pin the waves into a stable polar distribution. We refer to these dynamics as wave-pinning and we show that this phenomenon is distinct from Turing-instability-generated pattern formation that occurs in reaction-diffusion systems that appear to be very similar. We explain the mathematical basis of the phenomenon, relate it to spatial segregation of Rho GTPases, and show how it can account for spatial amplification and maintenance of polarity, as well as sensitivity to new stimuli typical in polarization of eukaryotic cells.

Original languageEnglish (US)
Pages (from-to)3684-3697
Number of pages14
JournalBiophysical journal
Issue number9
StatePublished - May 1 2008
Externally publishedYes

Bibliographical note

Funding Information:
The authors have been supported by a subcontract (to L.E.K.) from the National Science Foundation, United States, grant No. DMS-0240770 to Anders Carlsson, Washington University, St. Louis, Missouri; by the Mathematics of Information Technology and Complex Systems, Canada; and by a Natural Sciences and Engineering Research Council discovery grant held by L.E.K.


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