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DNA sensor cGAS-mediated immune recognition

The host takes use of pattern recognition receptors (PRRs) to defend against pathogen invasion or cellular damage. Among microorganism-associated molecular patterns detected by host PRRs, nucleic acids derived from bacteria or viruses are tightly supervised, providing a fundamental mechanism of host...

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Detalles Bibliográficos
Autores principales: Xia, Pengyan, Wang, Shuo, Gao, Pu, Gao, Guangxia, Fan, Zusen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084157/
https://www.ncbi.nlm.nih.gov/pubmed/27696330
http://dx.doi.org/10.1007/s13238-016-0320-3
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author Xia, Pengyan
Wang, Shuo
Gao, Pu
Gao, Guangxia
Fan, Zusen
author_facet Xia, Pengyan
Wang, Shuo
Gao, Pu
Gao, Guangxia
Fan, Zusen
author_sort Xia, Pengyan
collection PubMed
description The host takes use of pattern recognition receptors (PRRs) to defend against pathogen invasion or cellular damage. Among microorganism-associated molecular patterns detected by host PRRs, nucleic acids derived from bacteria or viruses are tightly supervised, providing a fundamental mechanism of host defense. Pathogenic DNAs are supposed to be detected by DNA sensors that induce the activation of NFκB or TBK1-IRF3 pathway. DNA sensor cGAS is widely expressed in innate immune cells and is a key sensor of invading DNAs in several cell types. cGAS binds to DNA, followed by a conformational change that allows the synthesis of cyclic guanosine monophosphate–adenosine monophosphate (cGAMP) from adenosine triphosphate and guanosine triphosphate. cGAMP is a strong activator of STING that can activate IRF3 and subsequent type I interferon production. Here we describe recent progresses in DNA sensors especially cGAS in the innate immune responses against pathogenic DNAs.
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spelling pubmed-50841572016-11-14 DNA sensor cGAS-mediated immune recognition Xia, Pengyan Wang, Shuo Gao, Pu Gao, Guangxia Fan, Zusen Protein Cell Review The host takes use of pattern recognition receptors (PRRs) to defend against pathogen invasion or cellular damage. Among microorganism-associated molecular patterns detected by host PRRs, nucleic acids derived from bacteria or viruses are tightly supervised, providing a fundamental mechanism of host defense. Pathogenic DNAs are supposed to be detected by DNA sensors that induce the activation of NFκB or TBK1-IRF3 pathway. DNA sensor cGAS is widely expressed in innate immune cells and is a key sensor of invading DNAs in several cell types. cGAS binds to DNA, followed by a conformational change that allows the synthesis of cyclic guanosine monophosphate–adenosine monophosphate (cGAMP) from adenosine triphosphate and guanosine triphosphate. cGAMP is a strong activator of STING that can activate IRF3 and subsequent type I interferon production. Here we describe recent progresses in DNA sensors especially cGAS in the innate immune responses against pathogenic DNAs. Higher Education Press 2016-09-30 2016-11 /pmc/articles/PMC5084157/ /pubmed/27696330 http://dx.doi.org/10.1007/s13238-016-0320-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Xia, Pengyan
Wang, Shuo
Gao, Pu
Gao, Guangxia
Fan, Zusen
DNA sensor cGAS-mediated immune recognition
title DNA sensor cGAS-mediated immune recognition
title_full DNA sensor cGAS-mediated immune recognition
title_fullStr DNA sensor cGAS-mediated immune recognition
title_full_unstemmed DNA sensor cGAS-mediated immune recognition
title_short DNA sensor cGAS-mediated immune recognition
title_sort dna sensor cgas-mediated immune recognition
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084157/
https://www.ncbi.nlm.nih.gov/pubmed/27696330
http://dx.doi.org/10.1007/s13238-016-0320-3
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