STING is a direct innate immune sensor of cyclic di-GMP
Dara L. Burdette,
Kathryn M. Monroe,
Katia Sotelo-Troha,
Jeff S. Iwig,
Barbara Eckert,
Mamoru Hyodo,
Yoshihiro Hayakawa and
Russell E. Vance ()
Additional contact information
Dara L. Burdette: University of California
Kathryn M. Monroe: University of California
Katia Sotelo-Troha: University of California
Jeff S. Iwig: University of California
Barbara Eckert: University of California
Mamoru Hyodo: Faculty of Pharmaceutical Science, Hokkaido University, Kita 12, Nishi 6, Kita-ku, Sapporo, Hokkaido 060-0812, Japan
Yoshihiro Hayakawa: Faculty of Engineering, Aichi Institute of Technology, 1247 Yachigusa, Yakusa, Toyota 470-0392, Japan
Russell E. Vance: University of California
Nature, 2011, vol. 478, issue 7370, 515-518
Abstract:
Bacterial metabolites recognized by STING Cyclic dinucleotides, used as signalling molecules in bacteria but not in mammalian cells, are recognized by the mammalian innate immune system, triggering the production of type I interferon. Here the mammalian protein STING (stimulator of IFN genes) is identified as the direct molecular sensor for cyclic diguanylate monophosphate and other cyclic dinucleotides. Previously, STING was thought to act solely as a downstream signalling adaptor. Cyclic dinucleotides are potent immunostimulants, and may prove useful therapeutically.
Date: 2011
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:478:y:2011:i:7370:d:10.1038_nature10429
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DOI: 10.1038/nature10429
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