Adipose mesenchymal stem cell-derived exosomal microRNAs ameliorate polycystic ovary syndrome by protecting against metabolic disturbances

被引:27
|
作者
Cao, Maosheng [1 ]
Zhao, Yun [1 ]
Chen, Tong [1 ]
Zhao, Zijiao [1 ]
Zhang, Boqi [1 ]
Yuan, Chenfeng [1 ]
Wang, Xin [1 ]
Chen, Lu [1 ]
Wang, Nan [1 ]
Li, Chunjin [1 ]
Zhou, Xu [1 ]
机构
[1] Jilin Univ, Coll Anim Sci, Changchun 130062, Peoples R China
基金
中国国家自然科学基金;
关键词
Polycystic ovary syndrome; Adipose mesenchymal stem cell; Infertility; Exosomes; miR-21-5p; HEPATIC ISCHEMIA-REPERFUSION; TISSUE; DIFFERENTIATION; TRANSPLANTATION; APOPTOSIS; PATHWAY; MIRNAS; WOMEN; BTG2; GENE;
D O I
10.1016/j.biomaterials.2022.121739
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polycystic ovary syndrome (PCOS) is the most common endocrine and metabolic disorder in women of child-bearing age. Adipose mesenchymal stem cells (AMSCs) secrete cytokines involved in the regulation of meta-bolism and immunity. However, it remains unclear whether exosomes secreted by AMSCs (AMSC-EXOs) can rescue the polycystic phenotype and metabolic dysfunction in PCOS ovaries. Here, we show that AMSC-EXOs can protect against metabolic disturbances, ameliorate ovarian polycystic, and improve fertility in a rat model of PCOS. AMSC-EXOs inhibited the expression of B-cell translocation gene 2 by transferring miR-21-5p to the livers of rats with PCOS, thus activating the IRS1/AKT pathway and increasing hepatic metabolism. The role of AMSC-EXOs in transferring miRNAs to the liver to improve metabolic dysfunction in PCOS and reproduction by rescuing a non-coding RNA pathway was also discovered. This study provides a theoretical basis for the use of rat adipose stem cells and their secreted exosomes to treat PCOS.
引用
收藏
页数:16
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