Exosome Derived From Human Umbilical Cord Mesenchymal Stem Cell Mediates MiR-181c Attenuating Burn-induced Excessive Inflammation

被引:349
作者
Li, Xiao [1 ]
Liu, Lingying [1 ]
Yang, Jing [1 ]
Yu, Yonghui [1 ]
Chai, Jiake [1 ]
Wang, Lingyan [2 ]
Ma, Li [1 ]
Yin, Huinan [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Affiliated Hosp 1, Dept Burn & Plast Surg, 51 Fucheng Rd, Beijing 100048, Peoples R China
[2] Peoples Liberat Army Gen Hosp, Affiliated Hosp 1, Dept Med Adm, 51 Fucheng Rd, Beijing 100048, Peoples R China
来源
EBIOMEDICINE | 2016年 / 8卷
基金
美国国家科学基金会;
关键词
Exosome; miR-181c; Burn; Inflammation; ACUTE LUNG INJURY; EXTRACELLULAR VESICLES; BIOLOGICAL-PROPERTIES; MICRORNAS; SECRETION; MECHANISM; MICROVESICLES; BIOGENESIS; EXPRESSION; RESPONSES;
D O I
10.1016/j.ebiom.2016.04.030
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mesenchymal stem cell (MSC)-derived exosomes have diverse functions in regulating wound healing and inflammation; however, the molecular mechanism of human umbilical cord MSC (hUCMSC)-derived exosomes in regulating burn-induced inflammation is not well understood. We found that burn injury significantly increased the inflammatory reaction of rats or macrophages exposed to lipopolysaccharide (LPS), increased tumor necrosis factor alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) levels and decreased IL-10 levels. hUCMSC-exosome administration successfully reversed this reaction. Further studies showed that miR-181c in the exosomes played a pivotal role in regulating inflammation. Compared to control hUCMSC-exosomes, hUCMSC-exosomes overexpressing miR-181c more effectively suppressed the TLR4 signaling pathway and alleviated inflammation in burned rats. Administration of miR-181c-expressing hUCMSC-exosomes or TLR4 knockdown significantly reduced LPS-induced TLR4 expression by macrophages and the inflammatory reaction. In summary, miR-181c expression in hUCMSC-exosomes reduces burn-induced inflammation by downregulating the TLR4 signaling pathway. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:72 / 82
页数:11
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