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      STING Signaling and Sterile Inflammation

      review-article
      ,
      Frontiers in Immunology
      Frontiers Media S.A.
      STING, cGAS, self-DNA, sterile inflammation, autophagy, type I IFN

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          Abstract

          Innate immunity is regulated by a broad set of evolutionary conserved receptors to finely probe the local environment and maintain host integrity. Besides pathogen recognition through conserved motifs, several of these receptors also sense aberrant or misplaced self-molecules as a sign of perturbed homeostasis. Among them, self-nucleic acid sensing by the cyclic GMP-AMP synthase (cGAS)/stimulator of interferon genes (STING) pathway alerts on the presence of both exogenous and endogenous DNA in the cytoplasm. We review recent literature demonstrating that self-nucleic acid detection through the STING pathway is central to numerous processes, from cell physiology to sterile injury, auto-immunity and cancer. We address the role of STING in autoimmune diseases linked to dysfunctional DNAse or related to mutations in DNA sensing pathways. We expose the role of the cGAS/STING pathway in inflammatory diseases, neurodegenerative conditions and cancer. Connections between STING in various cell processes including autophagy and cell death are developed. Finally, we review proposed mechanisms to explain the sources of cytoplasmic DNA.

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          Most cited references176

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          Pathogen recognition and innate immunity.

          Microorganisms that invade a vertebrate host are initially recognized by the innate immune system through germline-encoded pattern-recognition receptors (PRRs). Several classes of PRRs, including Toll-like receptors and cytoplasmic receptors, recognize distinct microbial components and directly activate immune cells. Exposure of immune cells to the ligands of these receptors activates intracellular signaling cascades that rapidly induce the expression of a variety of overlapping and unique genes involved in the inflammatory and immune responses. New insights into innate immunity are changing the way we think about pathogenesis and the treatment of infectious diseases, allergy, and autoimmunity.
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            Cyclic GMP-AMP synthase is a cytosolic DNA sensor that activates the type I interferon pathway.

            The presence of DNA in the cytoplasm of mammalian cells is a danger signal that triggers host immune responses such as the production of type I interferons. Cytosolic DNA induces interferons through the production of cyclic guanosine monophosphate-adenosine monophosphate (cyclic GMP-AMP, or cGAMP), which binds to and activates the adaptor protein STING. Through biochemical fractionation and quantitative mass spectrometry, we identified a cGAMP synthase (cGAS), which belongs to the nucleotidyltransferase family. Overexpression of cGAS activated the transcription factor IRF3 and induced interferon-β in a STING-dependent manner. Knockdown of cGAS inhibited IRF3 activation and interferon-β induction by DNA transfection or DNA virus infection. cGAS bound to DNA in the cytoplasm and catalyzed cGAMP synthesis. These results indicate that cGAS is a cytosolic DNA sensor that induces interferons by producing the second messenger cGAMP.
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              Mechanism and medical implications of mammalian autophagy

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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                01 October 2021
                2021
                : 12
                : 753789
                Affiliations
                [1] Experimental and Molecular Immunology and Neurogenetics Laboratory (INEM), Centre National de la Recherche Scientifique (CNRS), UMR7355 and University of Orleans , Orleans, France
                Author notes

                Edited by: Flavio Almeida Amaral, Federal University of Minas Gerais, Brazil

                Reviewed by: Akiko Takahashi, Japanese Foundation For Cancer Research, Japan; Pedro Elias Marques, KU Leuven, Belgium

                *Correspondence: Nicolas Riteau, nicolas.riteau@ 123456cnrs-orleans.fr

                This article was submitted to Inflammation, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2021.753789
                8517477
                34659260
                d97a5a67-f2c1-4eaf-bc2a-8a8fd4b77daa
                Copyright © 2021 Couillin and Riteau

                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) and the copyright owner(s) 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
                : 05 August 2021
                : 03 September 2021
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 176, Pages: 15, Words: 6552
                Categories
                Immunology
                Review

                Immunology
                sting,cgas,self-dna,sterile inflammation,autophagy,type i ifn
                Immunology
                sting, cgas, self-dna, sterile inflammation, autophagy, type i ifn

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