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      A guide to chemokines and their receptors

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          Abstract

          The chemokines (or chemotactic cytokines) are a large family of small, secreted proteins that signal through cell surface G protein‐coupled heptahelical chemokine receptors. They are best known for their ability to stimulate the migration of cells, most notably white blood cells (leukocytes). Consequently, chemokines play a central role in the development and homeostasis of the immune system, and are involved in all protective or destructive immune and inflammatory responses. Classically viewed as inducers of directed chemotactic migration, it is now clear that chemokines can stimulate a variety of other types of directed and undirected migratory behavior, such as haptotaxis, chemokinesis, and haptokinesis, in addition to inducing cell arrest or adhesion. However, chemokine receptors on leukocytes can do more than just direct migration, and these molecules can also be expressed on, and regulate the biology of, many nonleukocytic cell types. Chemokines are profoundly affected by post‐translational modification, by interaction with the extracellular matrix ( ECM), and by binding to heptahelical ‘atypical’ chemokine receptors that regulate chemokine localization and abundance. This guide gives a broad overview of the chemokine and chemokine receptor families; summarizes the complex physical interactions that occur in the chemokine network; and, using specific examples, discusses general principles of chemokine function, focusing particularly on their ability to direct leukocyte migration.

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          Chemokines: a new classification system and their role in immunity.

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            CCR7 and its ligands: balancing immunity and tolerance.

            A key feature of the immune system is its ability to induce protective immunity against pathogens while maintaining tolerance towards self and innocuous environmental antigens. Recent evidence suggests that by guiding cells to and within lymphoid organs, CC-chemokine receptor 7 (CCR7) essentially contributes to both immunity and tolerance. This receptor is involved in organizing thymic architecture and function, lymph-node homing of naive and regulatory T cells via high endothelial venules, as well as steady state and inflammation-induced lymph-node-bound migration of dendritic cells via afferent lymphatics. Here, we focus on the cellular and molecular mechanisms that enable CCR7 and its two ligands, CCL19 and CCL21, to balance immunity and tolerance.
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              Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists.

              Chemokine receptors are critical regulators of cell migration in the context of immune surveillance, inflammation, and development. The G protein-coupled chemokine receptor CXCR4 is specifically implicated in cancer metastasis and HIV-1 infection. Here we report five independent crystal structures of CXCR4 bound to an antagonist small molecule IT1t and a cyclic peptide CVX15 at 2.5 to 3.2 angstrom resolution. All structures reveal a consistent homodimer with an interface including helices V and VI that may be involved in regulating signaling. The location and shape of the ligand-binding sites differ from other G protein-coupled receptors and are closer to the extracellular surface. These structures provide new clues about the interactions between CXCR4 and its natural ligand CXCL12, and with the HIV-1 glycoprotein gp120.
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                Author and article information

                Contributors
                robert.nibbs@glasgow.ac.uk
                Journal
                FEBS J
                FEBS J
                10.1111/(ISSN)1742-4658
                FEBS
                The Febs Journal
                John Wiley and Sons Inc. (Hoboken )
                1742-464X
                1742-4658
                24 April 2018
                August 2018
                : 285
                : 16 ( doiID: 10.1111/febs.2018.285.issue-16 )
                : 2944-2971
                Affiliations
                [ 1 ] Institute of Infection, Inflammation & Immunity College of Medical, Veterinary and Life Sciences University of Glasgow UK
                Author notes
                [*] [* ] Correspondence

                R. J. B. Nibbs, Sir Graeme Davies Building, 120 University Place, Glasgow, G12 8TA Scotland, UK

                Fax: +44 141 330 4297

                Tel: +44 141 330 3960

                E‐mail: robert.nibbs@ 123456glasgow.ac.uk

                Author information
                http://orcid.org/0000-0002-8150-0044
                Article
                FEBS14466
                10.1111/febs.14466
                6120486
                29637711
                6e19a585-11db-4f6c-ac9a-92f7a70a70c4
                © 2018 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 January 2018
                : 25 March 2018
                : 03 April 2018
                Page count
                Figures: 4, Tables: 0, Pages: 28, Words: 19855
                Funding
                Funded by: Medical Research Council
                Award ID: N023625/1
                Award ID: M019764/1
                Funded by: Wellcome Trust
                Award ID: 206284/Z/17/Z
                Categories
                A Guide to
                A Guide to
                Custom metadata
                2.0
                febs14466
                August 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.4.7.1 mode:remove_FC converted:03.09.2018

                Molecular biology
                atypical chemokine receptor,cell migration,chemokine,chemokine receptor,glycosaminoglycan,immune surveillance,inflammation,leukocyte,oligomerization,protease

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