2′-O-Methyl-guanosine RNA fragments antagonize TLR7 and TLR8 to limit autoimmunity
Taif University · Hudson Institute of Medical Research · +12 more institutions
Abstract
Recognition of RNA fragments by Toll-like receptor 7 (TLR7) and TLR8 helps to initiate the innate immune response against pathogens. An outstanding question is why RNA fragments generated during clearance of apoptotic cells fail to activate TLR7 and TLR8 signaling. Here we show that select 2'-O-methyl (2'-OMe) guanosine RNA fragments, including those derived from host RNAs, function as potent TLR7 and TLR8 antagonists and reduce TLR7 sensing in vivo. Mechanistically, these fragments bind to an antagonistic site on these proteins via their 5'-end 2'-OMe guanosine. These findings indicate that host RNAs evade detection because abundant ribosomal 2'-OMe-modified fragments naturally antagonize TLR7 and TLR8.…
Citation impact
- FWCI
- 46.87
- Percentile
- 100%
- References
- 42
Authors
33- AAArwaf Alharbi
Taif University, Hudson Institute of Medical Research, Monash University
- SSSunil SapkotaCorresponding
Hudson Institute of Medical Research, Monash University
- ZZZhikuan Zhang
The University of Tokyo
- RJRuitao Jin
Australian National University
- ERErandi Rupasinghe
Hudson Institute of Medical Research, Monash University
Topics & keywords
- TLR7
- RNA
- Autoimmunity
- Innate immune system
- Guanosine
- Immune system
- Function (biology)