先天免疫系统
细胞生物学
核糖核酸
STAT1
小RNA
生物
信使核糖核酸
干扰素
信号转导
免疫系统
免疫学
基因
遗传学
作者
Henan Xu,Yan Jiang,Xiaoqing Xu,Xiaoping Su,Yang Liu,Yuanwu Ma,Yong Zhao,Zhongyang Shen,Bo Huang,Xuetao Cao
出处
期刊:Nature Immunology
[Springer Nature]
日期:2019-11-18
卷期号:20 (12): 1621-1630
被引量:147
标识
DOI:10.1038/s41590-019-0542-7
摘要
Interferon-γ (IFN-γ) is essential for the innate immune response to intracellular bacteria. Noncoding RNAs and RNA-binding proteins (RBPs) need to be further considered in studies of regulation of the IFN-γ-activated signaling pathway in macrophages. In the present study, we found that the microRNA miR-1 promoted IFN-γ-mediated clearance of Listeria monocytogenes in macrophages by indirectly stabilizing the Stat1 messenger RNA through the degradation of the cytoplasmic long noncoding RNA Sros1. Inducible degradation or genetic loss of Sros1 led to enhanced IFN-γ-dependent activation of the innate immune response. Mechanistically, Sros1 blocked the binding of Stat1 mRNA to the RBP CAPRIN1, which stabilized the Stat1 mRNA and, consequently, promoted IFN-γ-STAT1-mediated innate immunity. These observations shed light on the complex RNA-RNA regulatory networks involved in cytokine-initiated innate responses in host-pathogen interactions.
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