核糖核酸
生物
TLR3型
假尿苷
DNA
核苷
细胞生物学
Toll样受体
TLR9型
先天免疫系统
分子生物学
RNA沉默
受体
核酸
RNA干扰
TLR7型
基因
生物化学
基因表达
DNA甲基化
尿苷
作者
Katalin Karikó,Michael Buckstein,Houping Ni,Drew Weissman
出处
期刊:Immunity
[Elsevier]
日期:2005-08-01
卷期号:23 (2): 165-175
被引量:1955
标识
DOI:10.1016/j.immuni.2005.06.008
摘要
DNA and RNA stimulate the mammalian innate immune system through activation of Toll-like receptors (TLRs). DNA containing methylated CpG motifs, however, is not stimulatory. Selected nucleosides in naturally occurring RNA are also methylated or otherwise modified, but the immunomodulatory effects of these alterations remain untested. We show that RNA signals through human TLR3, TLR7, and TLR8, but incorporation of modified nucleosides m5C, m6A, m5U, s2U, or pseudouridine ablates activity. Dendritic cells (DCs) exposed to such modified RNA express significantly less cytokines and activation markers than those treated with unmodified RNA. DCs and TLR-expressing cells are potently activated by bacterial and mitochondrial RNA, but not by mammalian total RNA, which is abundant in modified nucleosides. We conclude that nucleoside modifications suppress the potential of RNA to activate DCs. The innate immune system may therefore detect RNA lacking nucleoside modification as a means of selectively responding to bacteria or necrotic tissue.
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