Species-specific recognition of single-stranded RNA via toll-like receptor 7 and 8

被引:3142
作者
Heil, F
Hemmi, H
Hochrein, H
Ampenberger, F
Kirschning, C
Akira, S
Lipford, G
Wagner, H
Bauer, S
机构
[1] Tech Univ Munich, Inst Med Microbiol Immunol & Hyg, D-81675 Munich, Germany
[2] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Suita, Osaka 5650871, Japan
[3] Japan Sci & Technol Corp, ERATO, Osaka 5650047, Japan
[4] Coley Pharmaceut Grp Inc, Wellesley, MA 02481 USA
关键词
D O I
10.1126/science.1093620
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Double-stranded ribonucleic acid (dsRNA) serves as a danger signal associated with viral infection and leads to stimulation of innate immune cells. In contrast, the immunostimulatory potential of single-stranded RNA (ssRNA) is poorly understood and innate immune receptors for ssRNA are unknown. We report that guanosine (G)- and uridine (U)-rich ssRNA oligonucleotides derived from human immunodeficiency virus-1 (HIV-1) stimulate dendritic cells (DC) and macrophages to secrete interferon-alpha and proinflammatory, as well as regulatory, cytokines. By using Toll-like receptor (TLR)-deficient mice and genetic complementation, we show that murine TLR7 and human TLR8 mediate species-specific recognition of GU-rich ssRNA. These data suggest that ssRNA represents a physiological ligand for TLR7 and TLR8.
引用
收藏
页码:1526 / 1529
页数:4
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