| Literature DB >> 33187730 |
Bindu D Paul1, Solomon H Snyder2, Vilhelm A Bohr3.
Abstract
Recognition of foreign or misplaced nucleic acids is one of the principal modes by which the immune system detects pathogenic entities. When cytosolic DNA is sensed, a signal is relayed via the cGAS-STING pathway: this involves the activation of cyclic GMP-AMP (cGMP-AMP) synthase (cGAS) and generation of the cyclic dinucleotide cGAMP, followed by the induction of stimulator of interferon genes (STING). The cGAS-STING pathway responds to viral, bacterial, and self-DNA. Whereas it generally mediates immune surveillance and is often neuroprotective, excessive engagement of the system can be deleterious. This is relevant in aging and age-related neurological diseases, where neuroinflammation contributes to disease progression. This review focuses on cGAS-STING signaling in aging, neurodegeneration, and neuroinflammation, and on therapeutic implications.Entities:
Keywords: Huntington’s disease; ataxia telangiectasia; cyclic GAMP; innate immune system; interferon-stimulated genes; senescence
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Year: 2020 PMID: 33187730 PMCID: PMC8662531 DOI: 10.1016/j.tins.2020.10.008
Source DB: PubMed Journal: Trends Neurosci ISSN: 0166-2236 Impact factor: 13.837