Exosomal miR-301 derived from mesenchymal stem cells protects myocardial infarction by inhibiting myocardial autophagy

被引:54
|
作者
Li, Yong [1 ,2 ]
Yang, Rong [1 ]
Guo, Bingyan [1 ]
Zhang, Hongbo [2 ]
Zhang, Hui [1 ]
Liu, Suyun [1 ]
Li, Yongjun [1 ]
机构
[1] Hebei Med Univ, Hosp 2, Dept Cardiol, 215 Heping West Rd, Shijiazhuang 050000, Hebei, Peoples R China
[2] Harris Int Peace Hosp, Dept Cardiol, 180 Renmin East Rd, Hengshui City 053000, Hebei, Peoples R China
关键词
BMSCs; Myocardial infarction; Exosomes; miR-301; Autophagy; TRANSPLANTATION;
D O I
10.1016/j.bbrc.2019.04.138
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: To investigate the protective effects of miR-301 in exosomes secreted by bone mesenchymal stem cells (BMSCs) on rats' myocardial infarction (MI). Methods: After isolation and culture, BMSCs were identified using flow cytometry. Then exosomes were then isolated. Rats MI models were established and they were divided into 4 groups: Sham group, Model group (injected with PBS), BMSC-Exos group (injected with exosomes secreted by BMSCs), BMSC-301-Exos group (injected with exosomes secreted by BMSCs transfected with miR-301 mimics). Cardiac function was assessed by cardiac echocardiography. Myocardial infarct area was measured by Masson trichrome staining mRNA and proteins expression were measured by qRT-PCR and western blot. Exosome morphology and myocardial cells autophagy were observed by transmission electron microscopy. Results: BMSCs were obtained. Rat MI models were successfully established. After rats were injected with exosomes secreted by BMSCs transfected with miR-301 mimics, MI tissues were found to have much higher miR-301 expression, LVEF, LVFS, P62 expression, and remarkably lower LVESD, LVEDD, MI area, LC3-II/LC3-I ratio and autophagosomes numbers compared with BMSC-Exos group (all P<0.05). Conclusion: miR-301 in exosomes secreted by BMSCs protected MI by inhibiting myocardial autophagy. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:323 / 328
页数:6
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