Micronuclei induced by radiation, replication stress, or chromosome segregation errors do not activate cGAS-STING
- PMID: 38749421
- DOI: 10.1016/j.molcel.2024.04.017
Micronuclei induced by radiation, replication stress, or chromosome segregation errors do not activate cGAS-STING
Abstract
The cyclic guanosine monophosphate (GMP)-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway plays a pivotal role in innate immune responses to viral infection and inhibition of autoimmunity. Recent studies have suggested that micronuclei formed by genotoxic stress can activate innate immune signaling via the cGAS-STING pathway. Here, we investigated cGAS localization, activation, and downstream signaling from micronuclei induced by ionizing radiation, replication stress, and chromosome segregation errors. Although cGAS localized to ruptured micronuclei via binding to self-DNA, we failed to observe cGAS activation; cGAMP production; downstream phosphorylation of STING, TBK1, or IRF3; nuclear accumulation of IRF3; or expression of interferon-stimulated genes. Failure to activate the cGAS-STING pathway was observed across primary and immortalized cell lines, which retained the ability to activate the cGAS-STING pathway in response to dsDNA or modified vaccinia virus infection. We provide evidence that micronuclei formed by genotoxic insults contain histone-bound self-DNA, which we show is inhibitory to cGAS activation in cells.
Keywords: DNA damage; IRF3; STING; cGAS; chromosome missegregation; innate immune response; micronuclei; radiation; replication stress.
Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests S.J.B. is a co-founder, VP Science Strategy, and shareholder at Artios Pharma Ltd. C.T.H. acknowledges grant support from Hoffman La Roche, has received speaker fees from AstraZeneca and Eli Lilly, and has a paid advisory role for GenesisCare UK.
Similar articles
-
The cGAS/STING/TBK1/IRF3 innate immunity pathway maintains chromosomal stability through regulation of p21 levels.Exp Mol Med. 2020 Apr;52(4):643-657. doi: 10.1038/s12276-020-0416-y. Epub 2020 Apr 13. Exp Mol Med. 2020. PMID: 32284536 Free PMC article.
-
DNA damage-triggered activation of cGAS-STING pathway induces apoptosis in human keratinocyte HaCaT cells.Mol Immunol. 2021 Mar;131:180-190. doi: 10.1016/j.molimm.2020.12.037. Epub 2021 Jan 8. Mol Immunol. 2021. PMID: 33423764
-
The cGas-Sting Signaling Pathway Is Required for the Innate Immune Response Against Ectromelia Virus.Front Immunol. 2018 Jun 14;9:1297. doi: 10.3389/fimmu.2018.01297. eCollection 2018. Front Immunol. 2018. PMID: 29963044 Free PMC article.
-
Potential cGAS-STING pathway functions in DNA damage responses, DNA replication and DNA repair.DNA Repair (Amst). 2024 Jan;133:103608. doi: 10.1016/j.dnarep.2023.103608. Epub 2023 Nov 30. DNA Repair (Amst). 2024. PMID: 38056369 Review.
-
The molecular mechanism of dsDNA sensing through the cGAS-STING pathway.Adv Immunol. 2024;162:1-21. doi: 10.1016/bs.ai.2024.02.003. Epub 2024 Mar 2. Adv Immunol. 2024. PMID: 38866436 Review.
Cited by
-
Cytosolic nucleic acid sensors and interferon beta-1 activation drive radiation-induced anti-tumour immune effects in human pancreatic cancer cells.Front Immunol. 2024 Sep 20;15:1286942. doi: 10.3389/fimmu.2024.1286942. eCollection 2024. Front Immunol. 2024. PMID: 39372406 Free PMC article.
-
Reduction of chromosomal instability and inflammation is a common aspect of adaptation to aneuploidy.EMBO Rep. 2024 Nov;25(11):5169-5193. doi: 10.1038/s44319-024-00252-0. Epub 2024 Sep 18. EMBO Rep. 2024. PMID: 39294502 Free PMC article.
-
DNA-sensing pathways in health, autoinflammatory and autoimmune diseases.Nat Immunol. 2024 Nov;25(11):2001-2014. doi: 10.1038/s41590-024-01966-y. Epub 2024 Oct 4. Nat Immunol. 2024. PMID: 39367124 Review.
-
Chromothripsis in cancer.Nat Rev Cancer. 2024 Nov 15. doi: 10.1038/s41568-024-00769-5. Online ahead of print. Nat Rev Cancer. 2024. PMID: 39548283 Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous