微泡
外体
吸入
间充质干细胞
细胞凋亡
吸入烟雾
免疫印迹
HMGB1
NF-κB
医学
癌症研究
炎症
药理学
免疫学
肺
化学
病理
内科学
麻醉
小RNA
生物化学
基因
作者
Bin Xu,Chunxia Gan,Sisi Chen,Jiaqi Li,Mingzhuo Liu,Guang‐hua Guo
出处
期刊:Life Sciences
[Elsevier BV]
日期:2020-07-01
卷期号:257: 118042-118042
被引量:41
标识
DOI:10.1016/j.lfs.2020.118042
摘要
To investigate the role of bone marrow mesenchymal stem cell (BMSC)-derived exosomes in smoke inhalation lung injury.In this study, we initially isolated exosomes from BMSCs and identified them by western blot and transmission electron microscopy. BMSC-derived exosomes were then used to treat in vitro and in vivo models of smoke inhalation lung injury. Pathologic alterations in lung tissue, the levels of inflammatory factors and apoptosis-related factors, and the expression of HMGB1 and NF-κB were determined to evaluate the therapeutic effect of BMSC-derived exosomes.We found that BMSC-derived exosomes could alleviate the injury caused by smoke inhalation. Smoke inhalation increased the levels of inflammatory factors and apoptosis-related factors and the expression of HMGB1 and NF-κB, and these increases were reversed by BMSC-derived exosomes. HMGB1 overexpression abrogated the exosome-induced decreases in inflammatory factors, apoptosis-related factors and NF-κB.Collectively, these results indicate that BMSC-derived exosomes can effectively alleviate smoke inhalation lung injury by inhibiting the HMGB1/NF-κB pathway, suggesting that exosome, a noncellular therapy, is a potential therapeutic strategy for inhalation lung injury.
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