微泡
炎症
TLR9型
心力衰竭
医学
机制(生物学)
外体
免疫学
生物
细胞生物学
小RNA
内科学
基因
遗传学
DNA甲基化
基因表达
哲学
认识论
作者
Wei Ye,Xiaojun Tang,Zhengquan Yang,Chu L,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.
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