Toll-like receptor 3 recognizes incomplete stem structures in single-stranded viral RNA
Megumi Tatematsu,
Fumiko Nishikawa,
Tsukasa Seya and
Misako Matsumoto ()
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Megumi Tatematsu: Hokkaido University Graduate School of Medicine
Fumiko Nishikawa: Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST)
Tsukasa Seya: Hokkaido University Graduate School of Medicine
Misako Matsumoto: Hokkaido University Graduate School of Medicine
Nature Communications, 2013, vol. 4, issue 1, 1-13
Abstract:
Abstract Endosomal Toll-like receptor 3 (TLR3) serves as a sensor of viral infection and sterile tissue necrosis. Although TLR3 recognizes double-stranded RNA, little is known about structural features of virus- or host-derived RNAs that activate TLR3 in infection/inflammatory states. Here we demonstrate that poliovirus-derived single-stranded RNA segments harbouring stem structures with bulge/internal loops are potent TLR3 agonists. Functional poliovirus-RNAs are resistant to degradation and efficiently induce interferon-α/β and proinflammatory cytokines in human and mouse cells in a TLR3-dependent manner. The N- and C-terminal double-stranded RNA-binding sites of TLR3 are required for poliovirus-RNA-mediated TLR3 activation. Like polyriboinosinic:polyribocytidylic acid, a synthetic double-stranded RNA, these RNAs are internalized into cells via raftlin-mediated endocytosis and colocalized with TLR3. Raftlin-associated RNA uptake machinery and the TLR3 RNA-sensing system appear to recognize an appropriate topology of multiple RNA duplexes in poliovirus-RNAs. Hence, TLR3 is a sensor of extracellular viral/host RNA with stable stem structures derived from infection or inflammation-damaged cells.
Date: 2013
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2857
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DOI: 10.1038/ncomms2857
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