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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 83-96 |
| Number of pages | 14 |
| Journal | Trends in neurosciences |
| Volume | 44 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2021 |
Keywords
- Huntington's disease
- ataxia telangiectasia
- cyclic GAMP
- innate immune system
- interferon-stimulated genes
- senescence
ASJC Scopus subject areas
- General Neuroscience
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