TLR7型
先天免疫系统
生物
核糖核酸
模式识别受体
干扰素
RNA沉默
Toll样受体
TLR9型
受体
促炎细胞因子
免疫系统
TLR3型
细胞生物学
钻机-I
病毒学
RNA干扰
免疫学
基因
基因表达
炎症
生物化学
DNA甲基化
作者
Florian Heil,Hiroaki Hemmi,Hubertus Hochrein,Franziska Ampenberger,Carsten J. Kirschning,Shizuo Akira,Grayson B. Lipford,Hermann Wagner,Stefan Bauer
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2004-02-24
卷期号:303 (5663): 1526-1529
被引量:3841
标识
DOI:10.1126/science.1093620
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-α 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.
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