Send to

Choose Destination
Sci Rep. 2015 Dec 4;5:17527. doi: 10.1038/srep17527.

Distinct predictive performance of Rac1 and Cdc42 in cell migration.

Author information

Graduate School of Informatics, Kyoto University, Sakyo, Kyoto, Japan.
Imaging Platform for Spatio-temporal Information, Graduate School of Medicine, Kyoto University, Sakyo, Kyoto, Japan.
Graduate School of Science, University of Tokyo, Bunkyo, Tokyo, Japan.
Graduate School of Biostudies, Kyoto University, Sakyo, Kyoto, Japan.


We propose a new computation-based approach for elucidating how signaling molecules are decoded in cell migration. In this approach, we performed FRET time-lapse imaging of Rac1 and Cdc42, members of Rho GTPases which are responsible for cell motility, and quantitatively identified the response functions that describe the conversion from the molecular activities to the morphological changes. Based on the identified response functions, we clarified the profiles of how the morphology spatiotemporally changes in response to local and transient activation of Rac1 and Cdc42, and found that Rac1 and Cdc42 activation triggers laterally propagating membrane protrusion. The response functions were also endowed with property of differentiator, which is beneficial for maintaining sensitivity under adaptation to the mean level of input. Using the response function, we could predict the morphological change from molecular activity, and its predictive performance provides a new quantitative measure of how much the Rho GTPases participate in the cell migration. Interestingly, we discovered distinct predictive performance of Rac1 and Cdc42 depending on the migration modes, indicating that Rac1 and Cdc42 contribute to persistent and random migration, respectively. Thus, our proposed predictive approach enabled us to uncover the hidden information processing rules of Rho GTPases in the cell migration.

[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Nature Publishing Group Icon for PubMed Central
Loading ...
Support Center