TY - JOUR
T1 - Polyinosinic acid is a ligand for toll-like receptor 3
AU - Marshall-Clarke, Stuart
AU - Downes, Joan E.
AU - Haga, Ismar R.
AU - Bowie, Andrew G.
AU - Borrow, Persephone
AU - Pennock, Joanne L.
AU - Grencis, Richard K.
AU - Rothwell, Paul
PY - 2007/8/24
Y1 - 2007/8/24
N2 - Innate immune responses are critical in controlling viral infections. Viral proteins and nucleic acids have been shown to be recognized by pattern recognition receptors of the Toll-like receptor (TLR) family, triggering downstream signaling cascades that lead to cellular activation and cytokine production. Viral DNA is sensed by TLR9, and TLRs 3, 7, and 8 have been implicated in innate responses to RNA viruses by virtue of their ability to sense double-stranded (ds) RNA (TLR3) or single-stranded RNA (murine TLR7 and human TLR8). Viral and synthetic dsRNAs have also been shown to be a potent adjuvant, promoting enhanced adaptive immune responses, and this property is also dependent on their recognition by TLR3. It has recently been shown that mRNA that is largely single-stranded is a ligand for TLR3. Here we have investigated the ability of single-stranded homopolymeric nucleic acids to induce innate responses by murine immune cells. We show for the first time that polyinosinic acid (poly(I)) activates B lymphocytes, dendritic cells, and macrophages and that these responses are dependent on the expression of both TLR3 and the adaptor molecule, Toll/IL-1 receptor domain-containing adaptor inducing IFN-β(TRIF). We therefore conclude that TLR3 is able to sense both single-stranded RNA and dsRNA. © 2007 by The American Society for Biochemistry and Molecular Biology, Inc.
AB - Innate immune responses are critical in controlling viral infections. Viral proteins and nucleic acids have been shown to be recognized by pattern recognition receptors of the Toll-like receptor (TLR) family, triggering downstream signaling cascades that lead to cellular activation and cytokine production. Viral DNA is sensed by TLR9, and TLRs 3, 7, and 8 have been implicated in innate responses to RNA viruses by virtue of their ability to sense double-stranded (ds) RNA (TLR3) or single-stranded RNA (murine TLR7 and human TLR8). Viral and synthetic dsRNAs have also been shown to be a potent adjuvant, promoting enhanced adaptive immune responses, and this property is also dependent on their recognition by TLR3. It has recently been shown that mRNA that is largely single-stranded is a ligand for TLR3. Here we have investigated the ability of single-stranded homopolymeric nucleic acids to induce innate responses by murine immune cells. We show for the first time that polyinosinic acid (poly(I)) activates B lymphocytes, dendritic cells, and macrophages and that these responses are dependent on the expression of both TLR3 and the adaptor molecule, Toll/IL-1 receptor domain-containing adaptor inducing IFN-β(TRIF). We therefore conclude that TLR3 is able to sense both single-stranded RNA and dsRNA. © 2007 by The American Society for Biochemistry and Molecular Biology, Inc.
U2 - 10.1074/jbc.M700188200
DO - 10.1074/jbc.M700188200
M3 - Article
C2 - 17573354
SN - 1083-351X
VL - 282
SP - 24759
EP - 24766
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 34
ER -