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Regulation of cGAS and STING signaling during inflammation and infection

Stimulator of interferon genes (STING) is a sensor of cyclic dinucleotides including cyclic GMP-AMP, which is produced by cyclic GMP-AMP synthase (cGAS) in response to cytosolic DNA. The cGAS–STING signaling pathway regulates both innate and adaptive immune responses, as well as fundamental cellular...

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Detalles Bibliográficos
Autores principales: Chauvin, Samuel D., Stinson, W. Alexander, Platt, Derek J., Poddar, Subhajit, Miner, Jonathan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316007/
https://www.ncbi.nlm.nih.gov/pubmed/37247757
http://dx.doi.org/10.1016/j.jbc.2023.104866
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author Chauvin, Samuel D.
Stinson, W. Alexander
Platt, Derek J.
Poddar, Subhajit
Miner, Jonathan J.
author_facet Chauvin, Samuel D.
Stinson, W. Alexander
Platt, Derek J.
Poddar, Subhajit
Miner, Jonathan J.
author_sort Chauvin, Samuel D.
collection PubMed
description Stimulator of interferon genes (STING) is a sensor of cyclic dinucleotides including cyclic GMP-AMP, which is produced by cyclic GMP-AMP synthase (cGAS) in response to cytosolic DNA. The cGAS–STING signaling pathway regulates both innate and adaptive immune responses, as well as fundamental cellular functions such as autophagy, senescence, and apoptosis. Mutations leading to constitutive activation of STING cause devastating human diseases. Thus, the cGAS–STING pathway is of great interest because of its role in diverse cellular processes and because of the potential therapeutic implications of targeting cGAS and STING. Here, we review molecular and cellular mechanisms of STING signaling, and we propose a framework for understanding the immunological and other cellular functions of STING in the context of disease.
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spelling pubmed-103160072023-07-04 Regulation of cGAS and STING signaling during inflammation and infection Chauvin, Samuel D. Stinson, W. Alexander Platt, Derek J. Poddar, Subhajit Miner, Jonathan J. J Biol Chem JBC Reviews Stimulator of interferon genes (STING) is a sensor of cyclic dinucleotides including cyclic GMP-AMP, which is produced by cyclic GMP-AMP synthase (cGAS) in response to cytosolic DNA. The cGAS–STING signaling pathway regulates both innate and adaptive immune responses, as well as fundamental cellular functions such as autophagy, senescence, and apoptosis. Mutations leading to constitutive activation of STING cause devastating human diseases. Thus, the cGAS–STING pathway is of great interest because of its role in diverse cellular processes and because of the potential therapeutic implications of targeting cGAS and STING. Here, we review molecular and cellular mechanisms of STING signaling, and we propose a framework for understanding the immunological and other cellular functions of STING in the context of disease. American Society for Biochemistry and Molecular Biology 2023-05-27 /pmc/articles/PMC10316007/ /pubmed/37247757 http://dx.doi.org/10.1016/j.jbc.2023.104866 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle JBC Reviews
Chauvin, Samuel D.
Stinson, W. Alexander
Platt, Derek J.
Poddar, Subhajit
Miner, Jonathan J.
Regulation of cGAS and STING signaling during inflammation and infection
title Regulation of cGAS and STING signaling during inflammation and infection
title_full Regulation of cGAS and STING signaling during inflammation and infection
title_fullStr Regulation of cGAS and STING signaling during inflammation and infection
title_full_unstemmed Regulation of cGAS and STING signaling during inflammation and infection
title_short Regulation of cGAS and STING signaling during inflammation and infection
title_sort regulation of cgas and sting signaling during inflammation and infection
topic JBC Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316007/
https://www.ncbi.nlm.nih.gov/pubmed/37247757
http://dx.doi.org/10.1016/j.jbc.2023.104866
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