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      I’m coming to GEF you: Regulation of RhoGEFs during cell migration

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          Abstract

          Cell migration is a highly regulated multistep process that requires the coordinated regulation of cell adhesion, protrusion, and contraction. These processes require numerous protein–protein interactions and the activation of specific signaling pathways. The Rho family of GTPases plays a key role in virtually every aspect of the cell migration cycle. The activation of Rho GTPases is mediated by a large and diverse family of proteins; the guanine nucleotide exchange factors (RhoGEFs). GEFs work immediately upstream of Rho proteins to provide a direct link between Rho activation and cell–surface receptors for various cytokines, growth factors, adhesion molecules, and G protein-coupled receptors. The regulated targeting and activation of RhoGEFs is essential to coordinate the migratory process. In this review, we summarize the recent advances in our understanding of the role of RhoGEFs in the regulation of cell migration.

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          Most cited references147

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          FAK-Src signalling through paxillin, ERK and MLCK regulates adhesion disassembly.

          Cell migration is a complex, highly regulated process that involves the continuous formation and disassembly of adhesions (adhesion turnover). Adhesion formation takes place at the leading edge of protrusions, whereas disassembly occurs both at the cell rear and at the base of protrusions. Despite the importance of these processes in migration, the mechanisms that regulate adhesion formation and disassembly remain largely unknown. Here we develop quantitative assays to measure the rate of incorporation of molecules into adhesions and the departure of these proteins from adhesions. Using these assays, we show that kinases and adaptor molecules, including focal adhesion kinase (FAK), Src, p130CAS, paxillin, extracellular signal-regulated kinase (ERK) and myosin light-chain kinase (MLCK) are critical for adhesion turnover at the cell front, a process central to migration.
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            Mouse and human dendritic cell subtypes.

            Dendritic cells (DCs) collect and process antigens for presentation to T cells, but there are many variations on this basic theme. DCs differ in the regulatory signals they transmit, directing T cells to different types of immune response or to tolerance. Although many DC subtypes arise from separate developmental pathways, their development and function are modulated by exogenous factors. Therefore, we must study the dynamics of the DC network in response to microbial invasion. Despite the difficulty of comparing the DC systems of humans and mice, recent work has revealed much common ground.
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              Coordination of Rho GTPase activities during cell protrusion

              The GTPases Rac1, RhoA and Cdc42 act in concert to control cytoskeleton dynamics1-3. Recent biosensor studies have shown that all three GTPases are activated at the front of migrating cells4-7 and biochemical evidence suggests that they may regulate one another: Cdc42 can activate Rac18, and Rac1 and RhoA are mutually inhibitory9-12. However, their spatiotemporal coordination, at the seconds and single micron dimensions typical of individual protrusion events, remains unknown. Here, we examine GTPase coordination both through simultaneous visualization of two GTPase biosensors and using a “computational multiplexing” approach capable of defining the relationships between multiple protein activities visualized in separate experiments. We found that RhoA is activated at the cell edge synchronous with edge advancement, whereas Cdc42 and Rac1 are activated 2 μm behind the edge with a delay of 40 sec. This indicates that Rac1 and RhoA operate antagonistically through spatial separation and precise timing, and that RhoA plays a role in the initial events of protrusion, while Rac1 and Cdc42 activate pathways implicated in reinforcement and stabilization of newly expanded protrusions.
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                Author and article information

                Journal
                Cell Adh Migr
                Cell Adh Migr
                KCAM
                Cell Adhesion & Migration
                Taylor & Francis
                1933-6918
                1933-6926
                Nov-Dec 2014
                31 October 2014
                : 8
                : 6
                : 535-549
                Affiliations
                Department of Biological Sciences; University of Toledo ; Toledo, OH USA
                Author notes
                [* ]Correspondence to: Rafael Garcia-Mata; Email: Rafael.GarciaMata@ 123456utoledo.edu
                Article
                983666
                10.4161/cam.28721
                4594598
                25482524
                e268196d-4e65-4545-acd1-5c8f73c06f82
                © 2014; The Author(s). Published with license by Taylor & Francis Group, LLC© Silvia M Goicoechea, Sahezeel Awadia, and Rafael Garcia-Mata

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

                History
                : 22 February 2014
                : 17 March 2014
                : 31 March 2014
                Page count
                Figures: 2, Tables: 1, References: 161, Pages: 15
                Categories
                Review

                Cell biology
                cell migration,rho gtpases,rho gefs,guanine nucleotide exchange factors,cell polarization,focal adhesions

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