间充质干细胞
细胞生物学
线粒体
细胞外
间质细胞
中性粒细胞胞外陷阱
微泡
再灌注损伤
细胞外小泡
生物
化学
缺血
癌症研究
免疫学
医学
生物化学
炎症
内科学
基因
小RNA
作者
Tongyu Lu,Jiebin Zhang,Jianye Cai,Jiaqi Xiao,Xin Sui,Xiaofeng Yuan,Rong Li,Yang Li,Jia Yao,Guoyue Lv,Xiaohong Chen,Haitian Chen,Kaining Zeng,Yasong Liu,Wenjie Chen,Guihua Chen,Yang Yang,Jun Zheng,Yingcai Zhang
出处
期刊:Biomaterials
[Elsevier]
日期:2022-04-02
卷期号:284: 121486-121486
被引量:61
标识
DOI:10.1016/j.biomaterials.2022.121486
摘要
As nanotherapeutics, mesenchymal stromal cell-derived extracellular vesicles (MSC-EVs) are considered a potent alternative for whole-cell therapy and are gradually entering the clinical field of liver diseases. In this study, neutrophil extracellular traps (NETs) formation in liver tissue was verified as a critical factor for liver ischaemia–reperfusion injury (IRI) in both clinical samples and animal models. Human umbilical cord-derived MSC-EVs (hUC-MSC-EVs) might function to reduce the NETs formation and subsequently improve liver IRI. Mechanistically, we showed that hUC-MSC-EVs contain functional mitochondria that are transferred to intrahepatic neutrophils. This effect triggers mitochondrial fusion and subsequently restores the mitochondrial status and functions in neutrophils to reduce NETs formation. Collectively, our findings suggest that MSC-EVs exert a nanotherapeutic effect on inhibiting local NETs formation by transferring functional mitochondria to intrahepatic neutrophils and repairing their mitochondrial function, which highlights the therapeutic value of hUC-MSC-EVs for liver IRI.
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