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      Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite

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          Abstract

          The removal of unwanted or damaged cells by phagocytes is achieved via a finely regulated cleaning process called efferocytosis. To characterize the mechanisms through which phagocytes control the intake of apoptotic cells, we investigated how the phagocyte’s appetite for engulfed cells may be coordinated by RhoA and Rac1 in the phagocytic cup. We used FRET biosensors to visualize the spatiotemporal dynamics of Rho-family GTPases, and found that RhoA, which is known to be downregulated during phagocytosis, was transiently upregulated at the phagocytic cup immediately prior to ingestion. Conversely, Rac1 was upregulated during the engulfment process and then downregulated prior to phagosomal maturation. Moreover, disturbance of the dynamic activities of RhoA led to uncontrolled engulfment, such as fast and undiscerning eating. Our results reveal that the temporal activity of RhoA GTPase alters the Rac1/RhoA balance at the phagocytic cup prior to ingestion, and that this plays a distinct role in orchestrating efferocytosis, with RhoA modulating the rate of engulfment to ensure that the phagocyte engulfs an appropriate amount of the correct material.

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          Most cited references37

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          Signaling from Rho to the actin cytoskeleton through protein kinases ROCK and LIM-kinase.

          The actin cytoskeleton undergoes extensive remodeling during cell morphogenesis and motility. The small guanosine triphosphatase Rho regulates such remodeling, but the underlying mechanisms of this regulation remain unclear. Cofilin exhibits actin-depolymerizing activity that is inhibited as a result of its phosphorylation by LIM-kinase. Cofilin was phosphorylated in N1E-115 neuroblastoma cells during lysophosphatidic acid-induced, Rho-mediated neurite retraction. This phosphorylation was sensitive to Y-27632, a specific inhibitor of the Rho-associated kinase ROCK. ROCK, which is a downstream effector of Rho, did not phosphorylate cofilin directly but phosphorylated LIM-kinase, which in turn was activated to phosphorylate cofilin. Overexpression of LIM-kinase in HeLa cells induced the formation of actin stress fibers in a Y-27632-sensitive manner. These results indicate that phosphorylation of LIM-kinase by ROCK and consequently increased phosphorylation of cofilin by LIM-kinase contribute to Rho-induced reorganization of the actin cytoskeleton.
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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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              The interaction between signal regulatory protein alpha (SIRPα) and CD47: structure, function, and therapeutic target.

              CD47 is a broadly expressed membrane protein that interacts with the myeloid inhibitory immunoreceptor SIRPα (also termed CD172a or SHPS-1). SIRPα is the prototypic member of the SIRP paired receptor family of closely related SIRP proteins. Engagement of SIRPα by CD47 provides a downregulatory signal that inhibits host cell phagocytosis, and CD47 therefore functions as a "don't-eat-me" signal. Here, we discuss recent structural analysis of CD47-SIRPα interactions and implications of this for the function and evolution of SIRPα and paired receptors in general. Furthermore, we review the proposed roles of CD47-SIRPα interactions in phagocytosis, (auto)immunity, and host defense, as well as its potential significance as a therapeutic target in cancer and inflammation and for improving graft survival in xenotransplantation.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                4 April 2017
                2017
                : 12
                : 4
                : e0174603
                Affiliations
                [1 ]Department of Biochemistry and Cell Biology, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Republic of Korea
                [2 ]ASAN Institute for Life Sciences, ASAN Medical Center, Seoul, Republic of Korea
                [3 ]Department of Convergence Medicine, University of Ulsan College of Medicine, Seoul, Republic of Korea
                [4 ]Department of Biochemistry, School of Medicine, Dongguk University, Gyeongju, Republic of Korea
                [5 ]Biomedical Research Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea
                [6 ]KU-KIST school, Korea University, Seoul, Republic of Korea
                Leiden University, NETHERLANDS
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: SYK SK ISK.

                • Data curation: SYK DJB.

                • Formal analysis: SYK DJB.

                • Funding acquisition: SK ISK.

                • Investigation: SYK SK DJB.

                • Methodology: SYK DJB.

                • Project administration: SYK SK ISK.

                • Resources: SYP GMP.

                • Supervision: SK ISK.

                • Validation: SYP GYL.

                • Visualization: SYK SK DJB.

                • Writing – original draft: SK.

                • Writing – review & editing: SYK SK SYP ISK.

                Author information
                http://orcid.org/0000-0003-1714-4521
                Article
                PONE-D-16-40964
                10.1371/journal.pone.0174603
                5380344
                28376111
                41b81e2f-c5ce-4a55-b612-01d2073f71b5
                © 2017 Kim et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 13 October 2016
                : 10 March 2017
                Page count
                Figures: 5, Tables: 0, Pages: 19
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100003725, National Research Foundation of Korea;
                Award ID: 2015R1D1A3A01019018
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100003725, National Research Foundation of Korea;
                Award ID: 2014R1A5A2009242
                Funded by: funder-id http://dx.doi.org/10.13039/501100003693, Korea Institute of Science and Technology;
                Award ID: Project No. 2E25270
                Award Recipient :
                This work was supported by the National Research Foundation of Korea(NRF) grant funded by the Korea government (2015R1D1A3A01019018); by the National Research Foundation of Korea(NRF) grant funded by the Korea government (2014R1A5A2009242); by the KIST Institutional Program (Project No. 2E25270). Author Soyoun Kim received a part of salary from the fund National Research Foundation of Korea (2014R1A5A2009242). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Cell Biology
                Cell Processes
                Phagocytosis
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Blood Cells
                White Blood Cells
                Phagocytes
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Immune Cells
                White Blood Cells
                Phagocytes
                Biology and Life Sciences
                Immunology
                Immune Cells
                White Blood Cells
                Phagocytes
                Medicine and Health Sciences
                Immunology
                Immune Cells
                White Blood Cells
                Phagocytes
                Biology and Life Sciences
                Cell Biology
                Cell Processes
                Cell Death
                Apoptosis
                Research and Analysis Methods
                Spectrum Analysis Techniques
                Spectrophotometry
                Fluorophotometry
                Fluorescence Resonance Energy Transfer
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Blood Cells
                White Blood Cells
                Macrophages
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Immune Cells
                White Blood Cells
                Macrophages
                Biology and Life Sciences
                Immunology
                Immune Cells
                White Blood Cells
                Macrophages
                Medicine and Health Sciences
                Immunology
                Immune Cells
                White Blood Cells
                Macrophages
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Stem Cells
                Hematopoietic Progenitor Cells
                Thymocytes
                Biology and Life Sciences
                Cell Biology
                Cellular Structures and Organelles
                Vesicles
                Liposomes
                Biology and Life Sciences
                Biochemistry
                Enzymology
                Enzymes
                Hydrolases
                Guanosine Triphosphatase
                Biology and Life Sciences
                Biochemistry
                Proteins
                Enzymes
                Hydrolases
                Guanosine Triphosphatase
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