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      Small GTPases and phosphoinositides in the regulatory mechanisms of macropinosome formation and maturation

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          Abstract

          Macropinosome formation requires the sequential activation of numerous signaling pathways that coordinate the actin-driven formation of plasma membrane protrusions (ruffles) and circular ruffles (macropinocytic cups), followed by the closure of these macropinocytic cups into macropinosomes. In the process of macropinosome formation, localized productions of phosphoinositides such as PI(4,5)P 2 and PI(3,4,5)P 3 spatiotemporally orchestrate actin polymerization and rearrangement through recruiting and activating a variety of actin-associated proteins. In addition, the sequential activation of small GTPases, which are known to be master regulators of the actin cytoskeleton, plays a pivotal role in parallel with phosphoinositides. To complete macropinosome formation, phosphoinositide breakdown and Rho GTPase deactivation must occur in appropriate timings. After the nascent macropinosomes are formed, phosphoinositides and several Rab GTPases control macropinosome maturation by regulating vesicle trafficking and membrane fusion. In this review, we summarize recent advances in our understanding of the critical functions of phosphoinositide metabolism and small GTPases in association with their downstream effectors in macropinocytosis.

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          Most cited references81

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          Virus entry by macropinocytosis.

          As obligatory intracellular parasites, viruses rely on host-cell functions for most aspects of their replication cycle. This is born out during entry, when most viruses that infect vertebrate and insect cells exploit the endocytic activities of the host cell to move into the cytoplasm. Viruses belonging to vaccinia, adeno, picorna and other virus families have been reported to take advantage of macropinocytosis, an endocytic mechanism normally involved in fluid uptake. The virus particles first activate signalling pathways that trigger actin-mediated membrane ruffling and blebbing. Usually, this is followed by the formation of large vacuoles (macropinosomes) at the plasma membrane, internalization of virus particles and penetration by the viruses or their capsids into the cytosol through the limiting membrane of the macropinosomes. We review the molecular machinery involved in macropinocytosis and describe what is known about its role in virus entry.
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            Defining macropinocytosis.

            Macropinocytosis represents a distinct pathway of endocytosis in mammalian cells. This actin-driven endocytic process is not directly co-ordinated by the presence of cargo but can be induced upon activation of growth factor signalling pathways. The capacity to dissect the contribution of macropinocytosis to cellular processes has been hampered by a lack of unique molecular markers and defining features. While aspects of macropinosome formation and maturation are common to those shared by the other endocytic pathways, a number of key differences have recently begun to emerge and will be discussed in this study. It is now well established that macropinocytosis significantly contributes to antigen presentation by the immune system and is exploited by a range of pathogens for cellular invasion and avoidance of immune surveillance.
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              Spatiotemporal dynamics of RhoA activity in migrating cells.

              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 body. However, there is evidence that RhoA also regulates membrane protrusion. 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 activity. Our data therefore show that different extracellular cues induce distinct patterns of RhoA signalling during membrane protrusion.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                30 September 2014
                2014
                : 5
                : 374
                Affiliations
                [1] 1Department of Histology and Cell Biology, School of Medicine, Kagawa University Miki, Japan
                [2] 2Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo Tokyo, Japan
                [3] 3Pathological Cell Biology Laboratory, Graduate School of Pharmaceutical Sciences, University of Tokyo Tokyo, Japan
                [4] 4Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital Toronto, ON, Canada
                Author notes

                Edited by: Hiroyuki Kabayama, RIKEN Brain Science Institute, Japan

                Reviewed by: Paul Anthony Gleeson, University of Melbourne, Australia; Robert Roger Kay, Medical Research Council, UK

                *Correspondence: Nobukazu Araki, Department of Histology and Cell Biology, School of Medicine, Kagawa University, 1750-1 Ikenobe, Miki, Kagawa 761-0793, Japan e-mail: naraki@ 123456med.kagawa-u.ac.jp

                This article was submitted to Membrane Physiology and Membrane Biophysics, a section of the journal Frontiers in Physiology.

                Article
                10.3389/fphys.2014.00374
                4179697
                25324782
                f8cc8c07-e94f-49a9-9a3c-fd4b215665b0
                Copyright © 2014 Egami, Taguchi, Maekawa, Arai and Araki.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 July 2014
                : 10 September 2014
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 93, Pages: 11, Words: 8226
                Categories
                Physiology
                Review Article

                Anatomy & Physiology
                macropinocytosis,small gtpases,phosphoinositides,rac1,optogenetics,myotubularin-related proteins

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