cGAS facilitates sensing of extracellular cyclic dinucleotides to activate innate immunity

H Liu, P Moura‐Alves, G Pei, HJ Mollenkopf… - EMBO …, 2019 - embopress.org
H Liu, P Moura‐Alves, G Pei, HJ Mollenkopf, R Hurwitz, X Wu, F Wang, S Liu, M Ma, Y Fei…
EMBO reports, 2019embopress.org
Cyclic dinucleotides (CDN s) are important second messenger molecules in prokaryotes
and eukaryotes. Within host cells, cytosolic CDN s are detected by STING and alert the host
by activating innate immunity characterized by type I interferon (IFN) responses.
Extracellular bacteria and dying cells can release CDN s, but sensing of extracellular CDN s
(eCDN s) by mammalian cells remains elusive. Here, we report that endocytosis facilitates
internalization of eCDN s. The DNA sensor cGAS facilitates sensing of endocytosed CDN s …
Abstract
Cyclic dinucleotides (CDNs) are important second messenger molecules in prokaryotes and eukaryotes. Within host cells, cytosolic CDNs are detected by STING and alert the host by activating innate immunity characterized by type I interferon (IFN) responses. Extracellular bacteria and dying cells can release CDNs, but sensing of extracellular CDNs (eCDNs) by mammalian cells remains elusive. Here, we report that endocytosis facilitates internalization of eCDNs. The DNA sensor cGAS facilitates sensing of endocytosed CDNs, their perinuclear accumulation, and subsequent STING‐dependent release of type I IFN. Internalized CDNs bind cGAS directly, leading to its dimerization, and the formation of a cGAS/STING complex, which may activate downstream signaling. Thus, eCDNs comprise microbe‐ and danger‐associated molecular patterns that contribute to host–microbe crosstalk during health and disease.
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