微泡
炎症
TLR9型
心力衰竭
医学
机制(生物学)
外体
免疫学
促炎细胞因子
先天免疫系统
免疫系统
生物
癌症研究
细胞生物学
小RNA
内科学
基因
遗传学
认识论
哲学
基因表达
DNA甲基化
作者
Wei Ye,Xiaojun Tang,Yang Zy,Liangliang Chu,Xin Zhang,Jing Jin,Jianxin Lyu
标识
DOI:10.1016/j.molimm.2017.03.011
摘要
Exosomes are small vesicles that contain proteins, DNA and RNA, and play an important role in inflammation; however, the underlying mechanism remains unclear. In the present study, we found increased plasma-derived exosomes in chronic heart failure patients compared with healthy controls. Further, our data demonstrated that plasma-derived exosomes carried mtDNA, and triggered an inflammatory response via the TLR9-NF-κB pathway, as well, the inflammatory effect was closely related to exosomal mtDNA copy number. However, the effect could be blocked by chloroquine (CQ), a TLR9 inhibitor. These findings reveal a new mechanism of exosome-induced inflammation, and provide a new perspective for intervention and treatment of inflammation-related diseases, such as chronic heart failure.
科研通智能强力驱动
Strongly Powered by AbleSci AI