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      PGH 1, the Precursor for the Anti-Inflammatory Prostaglandins of the 1-series, Is a Potent Activator of the Pro-Inflammatory Receptor CRTH2/DP2

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          Abstract

          Prostaglandin H 1 (PGH 1) is the cyclo-oxygenase metabolite of dihomo-γ-linolenic acid (DGLA) and the precursor for the 1-series of prostaglandins which are often viewed as “anti-inflammatory”. Herein we present evidence that PGH 1 is a potent activator of the pro-inflammatory PGD 2 receptor CRTH2, an attractive therapeutic target to treat allergic diseases such as asthma and atopic dermatitis. Non-invasive, real time dynamic mass redistribution analysis of living human CRTH2 transfectants and Ca 2+ flux studies reveal that PGH 1 activates CRTH2 as PGH 2, PGD 2 or PGD 1 do. The PGH 1 precursor DGLA and the other PGH 1 metabolites did not display such effect. PGH 1 specifically internalizes CRTH2 in stable CRTH2 transfectants as assessed by antibody feeding assays. Physiological relevance of CRTH2 ligation by PGH 1 is demonstrated in several primary human hematopoietic lineages, which endogenously express CRTH2: PGH 1 mediates migration of and Ca 2+ flux in Th2 lymphocytes, shape change of eosinophils, and their adhesion to human pulmonary microvascular endothelial cells under physiological flow conditions. All these effects are abrogated in the presence of the CRTH2 specific antagonist TM30089. Together, our results identify PGH 1 as an important lipid intermediate and novel CRTH2 agonist which may trigger CRTH2 activation in vivo in the absence of functional prostaglandin D synthase.

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          Most cited references72

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          Endocytosis and signalling: intertwining molecular networks.

          Cell signalling and endocytic membrane trafficking have traditionally been viewed as distinct processes. Although our present understanding is incomplete and there are still great controversies, it is now recognized that these processes are intimately and bidirectionally linked in animal cells. Indeed, many recent examples illustrate how endocytosis regulates receptor signalling (including signalling from receptor tyrosine kinases and G protein-coupled receptors) and, conversely, how signalling regulates the endocytic pathway. The mechanistic and functional principles that underlie the relationship between signalling and endocytosis in cell biology are becoming increasingly evident across many systems.
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            Evolving concepts in G protein-coupled receptor endocytosis: the role in receptor desensitization and signaling.

            G protein-coupled receptors (GPCRs) are seven transmembrane proteins that form the largest single family of integral membrane receptors. GPCRs transduce information provided by extracellular stimuli into intracellular second messengers via their coupling to heterotrimeric G proteins and the subsequent regulation of a diverse variety of effector systems. Agonist activation of GPCRs also initiates processes that are involved in the feedback desensitization of GPCR responsiveness, the internalization of GPCRs, and the coupling of GPCRs to heterotrimeric G protein-independent signal transduction pathways. GPCR desensitization occurs as a consequence of G protein uncoupling in response to phosphorylation by both second messenger-dependent protein kinases and G protein-coupled receptor kinases (GRKs). GRK-mediated receptor phosphorylation promotes the binding of beta-arrestins, which not only uncouple receptors from heterotrimeric G proteins but also target many GPCRs for internalization in clathrin-coated vesicles. beta-Arrestin-dependent endocytosis of GPCRs involves the direct interaction of the carboxyl-terminal tail domain of beta-arrestins with both beta-adaptin and clathrin. The focus of this review is the current and evolving understanding of the contribution of GRKs, beta-arrestins, and endocytosis to GPCR-specific patterns of desensitization and resensitization. In addition to their role as GPCR-specific endocytic adaptor proteins, beta-arrestins also serve as molecular scaffolds that foster the formation of alternative, heterotrimeric G protein-independent signal transduction complexes. Similar to what is observed for GPCR desensitization and resensitization, beta-arrestin-dependent GPCR internalization is involved in the intracellular compartmentalization of these protein complexes.
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              Prostaglandin D2 Selectively Induces Chemotaxis in T Helper Type 2 Cells, Eosinophils, and Basophils via Seven-Transmembrane Receptor Crth2

              Prostaglandin (PG)D2, which has long been implicated in allergic diseases, is currently considered to elicit its biological actions through the DP receptor (DP). Involvement of DP in the formation of allergic asthma was recently demonstrated with DP-deficient mice. However, proinflammatory functions of PGD2 cannot be explained by DP alone. We show here that a seven-transmembrane receptor, CRTH2, which is preferentially expressed in T helper type 2 (Th2) cells, eosinophils, and basophils in humans, serves as the novel receptor for PGD2. In response to PGD2, CRTH2 induces intracellular Ca2+ mobilization and chemotaxis in Th2 cells in a Gαi-dependent manner. In addition, CRTH2, but not DP, mediates PGD2-dependent cell migration of blood eosinophils and basophils. Thus, PGD2 is likely involved in multiple aspects of allergic inflammation through its dual receptor systems, DP and CRTH2.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                19 March 2012
                : 7
                : 3
                : e33329
                Affiliations
                [1 ]Molecular-, Cellular- and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany
                [2 ]Biomedical Research Centre, NDM Experimental Medicine, University of Oxford, Oxford, United Kingdom
                [3 ]Institute of Experimental and Clinical Pharmacology, Medical University Graz, Graz, Austria
                [4 ]Ernest Gallo Clinic and Research Center, University of California San Francisco, Emeryville, California, United States of America
                [5 ]Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, Denmark
                [6 ]Oxagen Ltd, Abingdon, Oxon, United Kingdom
                Medical School of Hannover, United States of America
                Author notes

                Conceived and designed the experiments: RS LX VK LM NK. Performed the experiments: RS LX VK LM NK. Analyzed the data: RS LX VK LM NK . Contributed reagents/materials/analysis tools: TU JLW. Wrote the paper: EK. Edited the manuscript and provided valuable comments: TU JLW. Contributed to data interpretation: AH RP. Contributed to conception and design of the study: AH RP. Edited the manuscript: AH RP TU JLW.

                Article
                PONE-D-11-24384
                10.1371/journal.pone.0033329
                3307725
                22442685
                efdac942-7689-4327-bfc6-fef0740708bc
                Schröder 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
                : 1 December 2011
                : 7 February 2012
                Page count
                Pages: 10
                Categories
                Research Article
                Biology
                Computational Biology
                Immunology
                Immunity
                Molecular Cell Biology
                Signal Transduction
                Signaling Cascades
                Signaling in Cellular Processes

                Uncategorized
                Uncategorized

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